8. Psycho-oncological Interventions – Psycho-oncology
8.1 Concept and General Principles for the Indication of Psycho-oncological Treatment
The indication for psycho-oncological interventions shall be made on the basis of the individual needs identified in accordance with recommendations 7.1. to 7.5, the setting, as well as the phase of the patient's illness (initial diagnosis, surgery, adjuvant therapy, recurrence-free phase, recurrence phase, palliative phase) and shall take into account the patient's wish for psycho-oncological support.
- Consensus
- Strong consensus (100%)
Change note
The indication for psycho-oncological interventions should be made according to the individual need identified according to recommendations 7.1. to 7.5, the setting, and the patient's phase of illness (initial diagnosis, surgery, adjuvant therapy, relapse-free phase, recurrence phase, palliative phase) and should take into account the patient's wishes.Patients with no or low distress (determined through screening and further diagnostics) shall be offered or given patient-oriented information and psychosocial counseling.
- Consensus
- Strong consensus (97,2%)
Change note
Patients with no or low burden (determined via screening and by further diagnostics) should be offered patient-oriented information and psychosocial counseling.In addition to Recommendation 8.2, patients with subsyndromal psychological distress (determined through screening and further diagnostics) shall be offered an individual and/or group psychotherapeutic/psycho-oncological intervention.
- Recommendation grade
- A: Starke Empfehlung für oder gegen ein Maßnahme - verwendete Ausdrucksweise = soll/soll nicht
- Level of evidence
- 1a
- Consensus
- Strong consensus (100%)
- References
- [582] [583] [584] [585] [586] [587] [588] [589] [590] [591] [592] [593] [594] [595] [596] [597] [598] [599] [600] [601] [602] [603] [604] [605] [606] [607] [608] [609] [610] [611] [612] [613] [614] [615] [616] [617] [618] [619] [620] [621] [622] [623] [624] [625] [626] [627] [628]
Change note
Patients with subsyndromal psychological distress (identified via screening and through further diagnostic testing) should be offered additional individual and/or group psychotherapeutic intervention.Patients with diagnosed psychiatric disorders shall be treated according to current disorder-specific guidelines.
- Consensus
- Strong consensus (100%)
Change note
Patients diagnosed with mental disorders should be cared for according to existing disorder-specific guidelines.Patients with an adjustment disorder according to ICD-10 (determined through screening and further diagnostics) shall be offered patient-centered information and psychosocial counseling and also an individual and/or group psychotherapeutic intervention.
- Consensus
- Strong consensus (100%)
Change note
Patients with adjustment disorder (identified via screening and further diagnostic testing) should be offered patient-centered information and psychosocial counseling, as well as additional individual and/or group psychotherapeutic intervention.The recommendations in this chapter refer to psycho-oncological interventions in the narrower sense.
The recommendations of Chapter 8.2 "Relaxation and Imaginative Procedures" to 8.5 "Psychotherapeutic Interventions" are based on a systematic literature search and review. A search was conducted for systematic reviews for the period 2010 - 2020, as well as a search for randomized controlled trials for the period 2015 - 2020 (Chapter 8.2-8.5). Similarly, the recommendations of Chapter 8.8 are based on a systematic literature search for the period 2012 - 2020. The data on the evaluation of effect sizes are based on the classification according to Cohen (Cohen’s d): d=0.2 corresponds to a small effect, d=0.5 to a medium effect, and d=0.8 to a large effect [629]. Short-term effects refer to measurement immediately after completion of an intervention, medium-term effects refer to measurement by a follow-up survey within a period of 6 months, and long-term effects refer to a catamnestic measurement period of more than six months [630]. The effect sizes described are always between-group effects (comparison of the intervention group with the control group), not pre-post effects within the intervention group. A detailed explanation of the systematic searches can be found in the Guideline Report.
Due to the insufficient evidence available, a systematic literature search was not performed for Chapters 8.6 and 8.7.
A psycho-oncological intervention in the narrower sense is defined as a non-pharmacological intervention in which psychological, psychotherapeutic, and social work methods are used alone or in combination, by professional therapists or counselors in a face-to-face interaction with cancer patients to reduce their psychological and social distress and improve their quality of life. A detailed explanation of this definition based on the PICO criteria can be found in the Guideline Report.
Furthermore, psycho-oncological interventions also include the Creative Arts Therapies.
In the course of updating the guideline, e-health based interventions (Chapter 8.4) as well as specific psycho-oncological interventions for patients in the palliative situation (Chapter 8.5.3.) have been added.
For further forms of intervention, please refer to Chapter 9 „Additional Therapies“.
As already mentioned at the beginning of the guideline, mind-body interventions for cancer patients such as yoga, qigong, and mindfulness-based methods are covered in the S3 guideline "Complementary Medicine in the Treatment of Oncological Patients" (AWMF register number: 032-055OL, https://www.awmf.org/leitlinien/detail/ll/032-055OL.html) and are therefore not part of this guideline. In addition, reference is also made here to the S3 guideline „Supportive Therapy for Oncological Patients“ (AWMF register number: 032-054OL, https://www.awmf.org/leitlinien/detail/ll/032-054OL.html) and the "Extended S3 Guideline Palliative Care for Patients with a Non-curable Cancer" (AWMF register number: 128-001OL, https://www.awmf.org/leitlinien/detail/ll/128-001OL.html).
In general:
- The indication for psycho-oncological interventions is based on individual need. The individual need is determined by psycho-oncological screening procedures such as self-description questionnaires or clinical screening questions, further diagnostic clarification and differential diagnosis, as well as the identification of the individual wishes of the patient with regard to psycho-oncological support. Further diagnostic procedures can be implemented in order to support the diagnosis (see Chapter 7.).
- Pycho-oncological measures are recommeded based upon the degree of distress or the type of psychological disorder identified.
In cases of no or low distress, information and psychosocial counseling are the appropriate interventions [582].
For subsyndromal distress, the updated evidence on psycho-oncological interventions shows that cancer patients benefit from psychoeducation, relaxation techniques, and psychotherapeutic procedures with respect to various complaints (see Chapter 8.2, 8.3 and 8.5). Art therapy should be offered, music and dance therapy as well as psycho-oncological e-health interventions can be offered (see Chapter 8.4 and 8.8).
Patients with ICD-10 diagnoses of a mental disorder are treated according to the available guidelines. Guidelines are available for the disorders or aspects covered in Chapter 7. Here, the somatic and social factors identified during the diagnosis and their interactions should be taken into account. The following two examples illustrate the consideration of cancer-specific somatic and social factors in guideline-based treatment:
- Progression anxiety as a "typical" subsyndromal distress in people with cancer must be differentiated from an anxiety disorder according to ICD-10 in the diagnosis process.
- For the diagnosis of a somatoform disorder according to ICD-10, it should be taken into account that physical symptoms (such as fatigue, nausea, hot flashes) can often occur as a result of oncological therapy.
For the ICD-10 diagnosis of an adjustment disorder (F43.2), there is currently no separate guideline available in German. Since adjustment disorders are common in cancer patients along with affective and anxiety disorders (see Chapter 6.2), the treatment of cancer patients with an adjustment disorder according to ICD-10 is specified in the corresponding recommendations in this chapter.
- According to the definition of evidence-based medicine, the preferences of the patient should be taken into consideration in addition to the best evidence and clinical expertise when determining indications. Consideration of patient preference for psycho-oncological interventions is particularly important because (a) patient motivation is an important efficacy factor of therapy and (b) there is little evidence to compare and test the efficacy of different psycho-oncological interventions so the choice between indicated interventions can be made on the basis of patient preference.
- The recommendation for psycho-oncological interventions should take into account the treatment setting (hospital, rehabilitation facility, outpatient setting) and the stage of disease (initial diagnosis, surgery, adjuvant therapy, recurrence-free phase, recurrence phase, palliative phase). For example, during an inpatient stay in an acute hospital, a psychoeducational program is not indicated due to the short length of stay. Here, priority will be given to an individual psychotherapeutic intervention supportive in nature or relaxation techniques.
- Based on the identified need for intervention, the diagnostic assessment, clinical evidence, patient preference, setting, and phase of illness, a clinical care algorithm can be formulated as follows:
Table 5: Overview of German S3 Guidelines on Mental Disorders
|
Disorder/Guideline |
AWMF number |
Source (http://www.awmf.org/leitlinien/aktuelle-leitlinien.html) |
|
Anxiety disorders |
051-028 |
|
|
Post-traumatic stress disorder |
055-001 |
|
|
Functional physical complaints |
051-001 |
|
|
Eating disorders |
051-026 |
|
|
Bipolar disorders |
038-019 |
|
|
Insomnia in adults Still being drafted at the time of this update, scheduled for completion in late 2022 |
063-001 |
|
|
Unipolar depression |
nvl-005 |
8.2 Relaxation and Imaginative Techniques
Relaxation techniques shall be offered to cancer patients, regardless of their level of distress, in order to reduce anxiety, depression, mental distress, fatigue, and nausea, as well as to improve quality of life.
- Recommendation grade
- A: Starke Empfehlung für oder gegen ein Maßnahme - verwendete Ausdrucksweise = soll/soll nicht
- Level of evidence
- 1a
- Consensus
- Strong consensus (100%)
- References
- [582] [631] [585] [632] [633] [634] [635] [636] [637] [638] [639]
Change note
Relaxation techniques should be offered to people with cancer regardless of the level of stress.- Recommendation grade
- 0: offene Empfehlung (Option) bzgl. einer Maßnahme - verwendete Ausdrucksweise = kann
- Level of evidence
- 1b
- Consensus
- Consent (77%)
- References
- [634] [640] [637] [638] [641] [642]
Change note
Relaxation techniques should be offered to people with cancer regardless of the level of stress.Relaxation techniques are a collective term for various methods that actively focus on physical, mental or spiritual relaxation. The most common methods are autogenic training, progressive muscle relaxation according to Jacobson (PMR), and guided imagery. Mindfulness-based methods (e.g. Mindfulness-based stress reduction (MBSR)) also belong to the relaxation techniques, however, as mentioned in Chapter 3.3, they are covered in Chapter 5 of the S3 guideline "Complementary Medicine in the Treatment of Oncological Patients" (AWMF register number: 032-055OL) and therefore not listed here. Relaxation techniques can be carried out by patients on their own after having received instruction and practice under professional guidance. This provides them with an instrument that enables them to reduce emotional tension (self-management) and strengthens their ability to regulate emotions (resource orientation). Compared to more intensive forms of psychotherapy, relaxation techniques are low-threshold and can be offered in an individual or group format. Likewise, relaxation techniques are often used as a component of other individual or group psycho-oncological interventions.
Relaxation techniques can be used in all phases of medical treatment for cancer, as well as in rehabilitation and follow-up care. They are particularly suitable for use before or during stressful diagnostic procedures, in preparation for radiotherapy or during chemotherapeutic treatments in order to reduce their side effects (e.g. nausea or anxiety).
Systematic literature review
The evaluation of the effectiveness of relaxation techniques in cancer patients and –survivors is based on five systematic reviews as well as ten RCTs. Three of the ten RCTs were already included in the systematic reviews; therefore, the results of these three studies are not reported separately in the presentation of results.
The five systematic reviews (three meta-analyses, two systematic reviews) included between five and 245 primary studies in the analysis. All reviews included mixed cancer populations. Primary studies included were from the US, China, Japan, UK, and the EU, among others. One meta-analysis addressed only the effectiveness of relaxation techniques in reducing anxiety [585], another exclusively fatigue [631], and one systematic review only pain reduction [639].
The sample size of the ten RCTs varied from 50 to 236 patients (N=1088), of which 28-100% were female. Studies were from Turkey (n=2) and Iran (n=2); the others were from Belgium, Italy, Greece, Romania, France, Thailand, and Taiwan (n=1 each). Often, the studies investigated specifically breast cancer (n=5) and breast and prostate cancer (n=2). One study specifically investigated head and neck cancer. The remaining studies (n=2) included patients with mixed cancer diagnoses. Common relaxation techniques offered were progressive muscle relaxation combined with guided imagery (n=2), progressive muscle relaxation alone (n=2), and hypnosis (n=2). Other relaxation methods offered were autogenic training (n=1) and other methods (n=3). The number of sessions ranged from one session to 12 sessions. Fatigue (n=4), pain (n=4), and anxiety (n=3) were most frequently assessed as primary endpoints. Furthermore, quality of life, depressiveness, and psychological distress (n=2 each) as well as nausea (n=1) represented primary endpoints in the RCTs.
Results
Quality of life, psychological distress, depressiveness, anxiety, fatigue, and nausea (Recommendation 8.6)
The short-term effectiveness of relaxation techniques on global quality of life was examined in a meta-analysis [582]. This was able to determine a significant short-term effect in favor of relaxation techniques (d=0.35). In addition, the results of three RCTs [634], [635], [636] were available, one of which was able to demonstrate a significant short-term effect in favor of relaxation techniques.
The medium-term effectiveness of relaxation techniques with regard to global quality of life was investigated in a meta-analysis [582]. This meta-analysis demonstrated a significant medium-term effect in favor of relaxation techniques (d=0.78). In addition, the results of three RCTs [634], [635], [636] were available, one of which was able to determine a significant medium-term effect in favor of relaxation techniques.
The short-term effectiveness of relaxation techniques with regard to mental stress (distress) was investigated in a meta-analysis [582]. This was able to determine a significant, short-term effect in favor of relaxation techniques (d=–0.29). In addition, the results of an RCT were available [637] which also demonstrated a significant short-term effect in favor of relaxation techniques.
The medium- and long-term effectiveness of relaxation techniques with regard to mental stress (distress) was investigated in only one meta-analysis [582]. This was unable to demonstrate any significant medium- or long-term effects in favor of relaxation techniques.
The short-term effectiveness of relaxation techniques with regard to depressiveness was investigated in one meta-analysis [582]. This showed a significant short-term effect in favor of relaxation techniques (d=–0.37). In addition, the results of one RCT [633] also demonstrated a significant short-term effect in favor of relaxation techniques.
The short-term effectiveness of relaxation techniques with regard to anxiety was examined in two meta-analyses [585], [582]. Both were able to establish significant, short-term effects in favor of relaxation techniques (d=–0.53 in each case). In addition, the results of two RCTs [633], [638] were available, one of which was able to demonstrate a significant, short-term effect in favor of relaxation techniques.
The medium-term effectiveness of relaxation techniques with regard to anxiety was investigated in one meta-analysis [582]. This was able to determine a significant, medium-term effect in favor of relaxation techniques (d=–1.12). In addition, the results of one RCT [638] were available which could not determine a significant, medium-term effect in favor of relaxation techniques.
The short-term effectiveness of relaxation techniques with regard to fatigue was investigated in one meta-analysis [631]. This demonstrated a significant short-term effect in favor of relaxation techniques (d=-0.77²). In addition, the results of four RCTs [633], [634], [635], [638] were available, two of which demonstrated significant short-term effects in favor of relaxation techniques.
No systematic reviews were available to evaluate the medium-term effectiveness of relaxation techniques on fatigue. Only the results of three RCTs were available [634], [635], [638], one of which demonstrated a significant, medium-term effect in favor of relaxation techniques.
The short- and medium-term efficacy of relaxation techniques with regard to chemotherapy-induced nausea was investigated in one systematic review [639], which descriptively described that significant short- and medium-term effects in favor of relaxation techniques were demonstrated in six of six RCTs included in the review. No additional RCTs were available.
² Effect significant only for patients after completion of treatment, not significant for patients receiving treatment.
Pain (Recommendation 8.7)
No systematic reviews were available to assess the short-term effectiveness of relaxation techniques with respect to pain. Only the results from six RCTs [634], [640], [637], [638], [641], [642] were available, four of which demonstrated significant short-term effects in favor of relaxation techniques. One of the six RCTs demonstrated a greater short-term reduction of pain in the control group (TAU) than in the relaxation group.
No systematic reviews were available to assess the medium-term effectiveness of relaxation techniques on pain either. Only the results of two RCTs [634], [638] were available, none of which found a significant medium-term effect in favor of relaxation techniques.
The findings on the effectiveness of relaxation techniques on pain in people with cancer can be considered heterogeneous. Pain represented the primary outcome in five of the six RCTs, and two of these five RCTs had a sufficiently large sample size according to a priori power analysis. Two of the six RCTs provided information on side effects and interactions, but these did not occur in either the control or relaxation groups. The methodological quality of all RCTs can be rated as moderate to low. The use of relaxation techniques to reduce pain is assessed by experts of the guideline group as common clinical practice. It should also be noted that evidence of efficacy exists for various forms of non-cancer pain. However, additional, methodologically high-quality studies are needed to formulate a more accurate recommendation for the use of relaxation techniques to reduce pain in people with cancer.
Supplementary evidence
In addition to the above findings per endpoint, a systematic review by Kapogiannis et al. [632] describes that significant effects in favor of relaxation techniques on at least one endpoint (including mood, anxiety, depressiveness, as well as nausea) were detectable in seven of 10 included RCTs.
Assessment of study quality
4/5 (80%) SRs had deficiencies in more than one critical assessment domain (critical low quality), 1/5 (20%) in one critical assessment domain (low quality). It should be noted that in 2/4 SRs, there was a downgrading of the quality assessment due to the lack of a list of excluded primary studies and their reasons for exclusion (critical domain 7, AMSTAR-2).
7/10 RCTs (70%) used an adequate method to generate the randomization sequence (selection bias), and in 7/10 RCTs (70%) the amount of missing data was sufficiently small (<20%) or missing data were appropriately imputed (attrition bias), and in 2/10 RCTs (20%) selective reporting of end points could be excluded through an existing study protocol (reporting bias). No conclusions could be drawn about the secrecy and unpredictability of group allocation of the RCTs (selection bias) (9/10, 90%), and in one RCT this was explicitly not possible. Due to the nature of the interventions used and the collection of endpoints by self-assessment, blinding of study personnel/participants (performance bias) was not possible in any of the RCTs and thus, nor was blinding of endpoint collection (detection bias), with the exception of one RCT.
7/10 RCTs performed a priori sample size estimation. 5/7 RCTs achieved their a priori planned sample size.
8.3 Psychoeducation
Psychoeducational interventions shall be offered to cancer patients, regardless of their level of distress, in order to reduce mental distress, anxiety, and pain, as well as to improve quality of life.
- Recommendation grade
- A: Starke Empfehlung für oder gegen ein Maßnahme - verwendete Ausdrucksweise = soll/soll nicht
- Level of evidence
- 1a
- Consensus
- Strong consensus (100%)
- References
- [582] [586] [643] [644] [645] [646] [647] [648] [649] [650] [600] [651] [652] [653] [654] [655] [656] [657] [658] [659] [660]
Change note
Psychoeducational interventions should be offered to people with cancer regardless of the level of distress.Psychoeducational interventions should be offered to cancer patients, regardless of the level of distress, in order to reduce depressiveness and fatigue.
- Recommendation grade
- B: Empfehlung für oder gegen eine Maßnahme - verwendete Ausdrucksweise = sollte/sollte nicht
- Level of evidence
- 1a
- Consensus
- Strong consensus (100%)
- References
- [592] [644] [582] [660] [600] [659] [651] [652] [653] [658] [654] [655]
Change note
Psychoeducational interventions should be offered to people with cancer regardless of the level of distress.Psychoeducational interventions are standardized, multimodal, interactive interventions that include a broad range of topics (Faller, 2016): Information about the illness, health-related behaviors, stress management, coping with disease, psychosocial support. „Standardized“ means the existence of a curriculum in which the learning objectives are defined and also a manual in which the learning objectives are specified and the didactic approach is defined. „Multimodal“ means the use of various, and especially interactive, activating didactic methods. This definition corresponds to the consensus definition of the Center for Patient Education. Giving information alone is not classified as patient education. Psychoeducation is offered in individual or group format.
Systematic literature review
The evaluation of the effectiveness of psychoeducational interventions in cancer patients and -survivors is based on eleven systematic reviews and 13 RCTs.
The eleven systematic reviews (eight meta-analyses, three systematic reviews) included between ten and 198 primary studies in the analysis. Nine of the reviews included mixed cancer populations, and in three cases [646], [647], [648], tumor-related pain also had to be present. One review examined lung cancer. The primary studies included were from the USA, Canada, Australia, China, and the EU, among others. One meta-analysis looked exclusively at the efficacy of psychoeducation in increasing quality of life [661], another looked exclusively at anxiety reduction [585], three systematic reviews looked only at pain reduction [646], [646], [647], [648], [647], and one systematic review looked at efficacy in reducing fatigue [662].
The sample size of the 13 RCTs varied between 40 and 2,140 patients (N=3,931), of which 15.5-100% were female. The studies were mostly from China (n=4) and Singapore (n=2). The remaining studies were from Iran, Qatar, Malaysia, Taiwan, France, Germany, and Sweden (n=1 each). Most studies specifically investigated breast cancer (n=4) or no specific cancer type (n=4). Further types of cancer specifically represented were laryngeal cancer, gynecologic cancers, bladder cancer, lung cancer, and anal and colorectal cancers (n=1 each). In most cases, psychoeducation was provided in the form of individual sessions (n=6); three studies examined a psychoeducational intervention presented in a group format. Three studies supplemented psychoeducation with other interventions, such as a training manual (n=1), self-management skills training (n=1), as well as a rehabilitation program (n=1). The number of psychoeducational intervention sessions presented ranged from one session to eight sessions. The most frequently assessed primary endpoints of the RCTs represented anxiety (n=7), depressiveness (n=6), and quality of life (n=6). Furthermore, pain (n=2), fatigue (n=2), sexual function (n=1), nausea (n=1), and psychological distress (n=1) were also collected as primary endpoints.
Results
Quality of life, psychological distress, anxiety, and pain (Recommendation 8.8)
The short-term effectiveness of psychoeducational interventions on global quality of life was examined in four meta-analyses [586], [644], [645], [582], three of which identified significant short-term effects in favor of psychoeducational interventions (0.19 < d <0.20³). In addition, the results of seven RCTs [660], [650], [600], [652], [653], [655], [657], [656] were available, two of which were able to demonstrate significant, short-term effects in favor of psychoeducational interventions. One of the seven RCTs provided mixed results and found a significant, short-term effect in favor of psychoeducational interventions for psychological quality of life, but not for physical quality of life.
The medium-term effectiveness of psychoeducational interventions on global quality of life was examined in one meta-analysis [582]. This failed to find a significant medium-term effect in favor of psychoeducational interventions. In addition, the results of two RCTs [600], [656] were available, neither of which could demonstrate a significant, medium-term effect in favor of psychoeducational interventions.
The long-term effectiveness of psychoeducational interventions regarding global quality of life was investigated in one meta-analysis [582]. This was able to demonstrate a significant long-term effect in favor of psychoeducational interventions (d=0.18). The result of one RCT [656] was also available, however, a significant long-term effect in favor of the psychoeducational intervention was not demonstrated.
³ Bennett 2016 report a non-standardized MD = 11.47 in global quality of life (EORTC QLQ-C30)
The short-term effectiveness of psychoeducational interventions on psychological distress was examined in one meta-analysis [582]. This was able to determine a significant short-term effect in favor of psychoeducational interventions (d=–0.18). In addition, the result of one RCT [657] was available which found no significant short-term effect in favor of psychoeducation.
The medium-term effectiveness of psychoeducational interventions with regard to psychological distress was also examined in a meta-analysis [582]. This was able to demonstrate a significant medium-term effect in favor of psychoeducational interventions (d=–0.30). No additional RCTs were available.
The long-term effectiveness of psychoeducational interventions on psychological distress was examined in one meta-analysis [582]. This failed to demonstrate a significant, long-term effect in favor of psychoeducational interventions. No additional RCTs were available.
The short-term effectiveness of psychoeducational interventions on anxiety was examined in three meta-analyses [585], [644], [582] , all of which were able to determine significant, short-term effects in favor of psychoeducational interventions (–0.18 < d < –1.47). In addition, the results of ten RCTs [649], [660], [600], [659], [651], [652], [653], [658], [655], [657] were available, five of which demonstrated significant, short-term effects in favor of psychoeducational interventions.
The medium-term effectiveness of psychoeducational interventions on anxiety was examined in one meta-analysis [582]. This demonstrated a significant medium-term effect in favor of psychoeducational interventions (d=–0.24). In addition, the result of one RCT [600] was available which also demonstrated a significant medium-term effect in favor of psychoeducation.
The long-term effectiveness of psychoeducational interventions on anxiety was also examined in one meta-analysis [582]. This found no significant long-term effect in favor of psychoeducational interventions. No additional RCTs were available.
The short-term efficacy of psychoeducational interventions on pain was examined in two meta-analyses [646][647], both of which found a significant short-term effect in favor of psychoeducational interventions (d=-0.11 and d=-0.27). Furthermore, the systematic review by Oldenmenger et al. [648] describes that eight of 26 included RCTs (31%) reported significant pain differences between groups in favor of the psychoeducation group. In addition, the results of two RCTs were available from our search [650], [654], one of which demonstrated a significant short-term effect in favor of psychoeducation.
No systematic reviews were available on the medium-term effectiveness of psychoeducational interventions regarding pain. Only the result of one RCT [650] was available, which found a significant, medium-term effect in favor of psychoeducation.
Depressiveness and fatigue (Recommendation 8.9)
The short-term efficacy of psychoeducational interventions on depressivity was examined in three meta-analyses [592], [644], [582], one of which was able to determine a significant, short-term effect in favor of psychoeducational interventions (d=–0.18). In addition, the results of eight RCTs [660], [600], [659], [651], [652], [653], [658], [655]) were available, four of which found significant, short-term effects in favor of psychoeducational interventions.
The medium-term effectiveness of psychoeducational interventions on depressivity was examined in one meta-analysis [582]. This was able to determine a significant, medium-term effect in favor of psychoeducational interventions (d=–0.23). In addition, the result of one RCT [600] was available which could also prove a significant, medium-term effect in favor of psychoeducational interventions.
The long-term efficacy of psychoeducational interventions on depressivity was examined in one meta-analysis [582]. This found no significant long-term effect in favor of psychoeducational interventions. No additional RCTs were available.
The short-term effectiveness of psychoeducational interventions on fatigue was examined in one meta-analysis [644]. This demonstrated a significant short-term effect in favor of psychoeducational interventions (d=-0.27). Furthermore, the systematic review by Du et al. [662] describes that five of the ten RCTs included in the review found a significant effect in favor of psychoeducation⁴. In addition, the results of two RCTs were available from our search [653], [654] but none of these found a significant short-term effect in favor of psychoeducation.
Nausea and sexual dysfunction (Statement 8.10)
No systematic reviews were available on the short-term effectiveness of psychoeducational interventions regarding nausea. Only the result of one RCT [654] was available which demonstrated no significant short-term effect in favor of psychoeducation.
No systematic reviews were available on the short-term effectiveness of psychoeducational interventions regarding sexual function. Only the result of one RCT [649] was available, here significant short-term effects in favor of psychoeducation on one of five subscales of the multidimensional questionnaire were demonstrated.
The studies on the reduction of nausea as well as sexual dysfunction are not sufficiently reliable. The guideline group therefore reserves the right to refrain from making a recommendation for or against the use of psychoeducational interventions by cancer patients and these complaints. Further studies of high methodological quality are needed to formulate a recommendation.
⁴ In 8 out of 10 RCTs included in the review from Du et al. 2015 [662], sport and exercise therapy were included in the psychoeducational interventions.
Supporting evidence
In addition to the above-mentioned findings per endpoint, a systematic review by Li et al. [663] shows that in 12 of 15 included RCTs there were significant effects in favor of psychoeducation on at least one primary endpoint (including quality of life, mental distress, pain, fatigue).
Assessment of study quality
8/11 (73%) SRs had deficiencies in more than one critical assessment domain (critical low quality) and 1/11 (9%) SRs in one critical assessment domain (low quality). 1/11 (9%) SRs had no critical but more than one non-critical deficiency (moderate quality), and one (9%) SR had no critical and only one non-critical deficiency (high quality). It should be noted that 2/10 SRs had a downgraded quality score due to the lack of a list of excluded primary studies and their reasons for exclusion (critical domain 7, AMSTAR-2).
9/13 RCTs (69%) used an adequate method to generate the randomization sequence (selection bias), 2/13 RCTs (15%) ensured secrecy and unpredictability of group allocation (selection bias), and in 6/13 RCTs (46%), the amount of missing data was sufficiently small (<20%) or missing data were appropriately imputed (attrition bias). Due to the nature of the interventions used and the collection of endpoints by self-assessment, blinding of study personnel/participants (performance bias) and thus blinding of endpoint collection (detection bias) were not possible in any of the RCTs. No statement could be made about the selective reporting of endpoints(reporting bias) due to the lack of study protocols.
10/13 RCTs performed a priori sample size estimation. 7/10 RCTs achieved their a priori planned sample size.
8.4 Psycho-oncology E-health Interventions
Psycho-oncological e-health interventions should be offered to cancer patients, regardless of the level of distress, in order to improve quality of life.
Psycho-oncological e-health interventions can be offered to cancer patients regardless of their level of distress, in order to reduce mental distress, depressiveness, anxiety, and fatigue.
- Recommendation grade
- 0: offene Empfehlung (Option) bzgl. einer Maßnahme - verwendete Ausdrucksweise = kann
- Level of evidence
- 1a
- Consensus
- Strong consensus (100%)
- References
- [667] [666] [665] [682] [669] [668] [670] [683] [684] [672] [685] [673] [674] [675] [686] [687] [688] [676] [677] [678] [679] [689] [680] [690] [691] [692] [693] [681]
The German Federal Ministry of Health uses the term "e-health" to refer to applications and services that use the possibilities of modern information and communication technologies (ICT) to support the treatment and care of patients (https://www.bundesgesundheitsministerium.de/service/begriffe-von-a-z/e/e-health.html). In the context of psycho-oncological care, the use of health apps or websites, as well as telemedicine services, are of primary importance. In terms of content, the interventions are usually multimodal. In practice, educational, counseling and low-threshold psychotherapeutic services are implemented and,through the use of an ICT, can be used regardless of location. Psycho-oncological care services can thus be made available to patients who live in regions with a low density of care and/or who are unable to take advantage of face-to-face services due to psychological or physical limitations.
In accordance with the definition of psycho-oncological interventions (in Chapter 8.1), the systematic literature review only included studies that involved personal interaction between professional therapists and cancer patients and dealt with psycho-oncological issues. For example, personal interaction could be via telephone, videoconference, or face-to-face contacts in addition to the use of websites or apps.
Digital health applications (DiGA) are also becoming increasingly important. Apps and browser-based applications tested by the Federal Institute for Drugs and Medical Devices (BfArM) for evidence-based positive care effects are now available for numerous areas of application, including oncology (https://diga.bfarm.de/de). It should be specifically noted once again that the pure use of health apps and websites, as well as video or audio recordings, or exclusive contact by mail, chats or forums, was excluded in the following systematic literature search.
It should be emphasized at this point that, in the viewpoint of the guideline group, psycho-oncological e-health interventions in clinical practice should not replace psycho-oncological services based on personal contact, but rather should be offered in addition to these services, especially when accessibility barriers exist.
Systematic literature review
The evaluation of the effectiveness of e-health/telehealth interventions in cancer patients and survivors is based on five systematic reviews and 28 RCTS from 30 publications⁵. Three of the 28 RCTs were already included in at least one of the systematic reviews, therefore, the results of these three studies are not reported separately in the results.
The five systematic reviews (four meta-analyses, one systematic review) included between 11 and 20 primary studies in the analysis. Cancer types studied were breast cancer (n=2) and mixed cancer populations (n=3). Primary studies included were from the US, Australia, China, Canada, UK, and the EU, among others. One meta-analysis focused exclusively on the efficacy of psycho-oncology e-health interventions on improving quality of life [664], all others reported outcomes on multiple relevant endpoints.
The sample size of the 28 RCTs varied between 38 and 254 patients (N=3,125), of which 0-100% were female. The studies were largely from the United States (n=15), Netherlands (n=3), and Australia (n=3); the remainder of the studies were from China (n=2), Singapore, Norway, France, Germany, and Sweden (n=1 each). The most common target group of e-health/telehealth interventions were breast cancer patients (n=10); other cancer types studied were prostate cancer (n=3) lung cancer (n=3), (colorectal) cancer (n=2), black skin cancer, cervical cancer, esophageal cancer, rectal and anal cancer, and leukemia (n=1 each). Five studies included patients with different cancer diagnoses. Intervention was frequently offered by telephone (n=16) and videoconferencing (n=5). In five studies, supplemental analog or digital materials were given. Some studies combined contact via telephone or video contacts together with face-to-face contacts (n=4). Other forms of delivery represented online modules (n=2) and apps (n=1) combined with face-to-face contacts. Content often involved cognitive-behavioral therapy elements (n=12) or general psychosocial support (n=9, including couples counseling). Furthermore, psychoeducation (n=3), acceptance and commitment therapy (ACT; n=1), as well as imagery-based (n=1) and other (n=2) approaches were offered. The number of intervention sessions offered ranged from a single session to weekly sessions over 24 weeks or sessions with larger time intervals inbetween of up to six months. Anxiety (n=12), depressiveness (n=11), and quality of life (n=7) represented the most common primary endpoints in the RCTs. Furthermore, fatigue (n=5), sexual function/satisfaction (n=5), mental distress (n=2), and pain (n=1) were collected as primary endpoints in the RCTs.
⁵ Dieng et al. 2020 [664] and Dieng et al. 2016 [665], as well as Chambers et al. 2015 [690] and Chambers et al. 2019 [691] all refer to the same sample but report results of additional points of measurement.
Results
Quality of life (Recommendation 8.11)
The short-term effectiveness of psycho-oncology e-health interventions on global quality of life was examined in four meta-analyses [664], [665], [666], [667], three of which identified significant short-term effects in favor of psycho-oncology e-health interventions (0.54 ≤ d ≤ 0.75). In addition, the results of ten RCTs [670], [672], [673], [674], [675], [676], [677], [678],[679], [680] were available, three of which were able to establish significant, short-term effects in favor of psycho-oncological e-health interventions.
The medium-term effectiveness of psycho-oncological e-health interventions with respect to global quality of life has not been investigated in any systematic review. However, the results of eight RCTs [669], [668], [671], [672], [676], [677], [678], [679], [681] were available, one of which demonstrated a significant medium-term effect in favor of the psycho-oncological e-health intervention.
No systematic reviews were available to assess the long-term effectiveness of psycho-oncology e-health interventions on global quality of life. Only the results of two RCTs were available [669], [668], [681] , one of which demonstrated a significant long-term effect in favor of the psycho-oncological e-health intervention.
Psychological distress, depressiveness, anxiety, and fatigue (Recommendation 8.12)
The short-term effectiveness of psycho-oncological e-health interventions with regard to psychological distress was investigated in one meta-analysis [667]. This could not determine a significant effect. In addition, the results of six RCTs [670], [673], [675], [677], [690], [693] were available, three of which were able to demonstrate a significant short-term effect in favor of psycho-oncological e-health interventions.
No systematic reviews were available to assess the medium-term effectiveness of psycho-oncological e-health interventions with regard to psychological distress. Only three RCTs were available [677], [690], [681], one of which was able to determine a significant medium-term effect in favor of the psycho-oncological e-health intervention.
The long-term effectiveness of psycho-oncological e-health interventions was not investigated in any systematic review. Only one RCT [681] was available, a significant long-term effect in favor of the psycho-oncological e-health intervention could not be determined.
The short-term efficacy of psycho-oncology e-health interventions with respect to depression was examined in two meta-analyses [666], [667]. Neither meta-analysis demonstrated significant short-term effects in favor of psycho-oncological e-health interventions. In addition, the results of 17 RCTs [670], [683], [672], [685], [674], [686], [687], [688], [676], [677], [678], [679], [689], [690], [691], [692], [693] were available, five of which were able to identify significant short-term effects in favor of psycho-oncological e-health interventions.
No systematic reviews were available to assess the medium-term effectiveness of psycho-oncological e-health interventions with regard to depression. However, the results of twelve RCTs [668], [669], [672], [685], [686], [687], [688], [676], [677], [678], [679], [690], [691] were available, one of which demonstrated a significant medium-term effect in favor of the psycho-oncological e-health intervention.
The long-term efficacy of psycho-oncological e-health interventions with regard to depression has not been investigated in any systematic review. Only the results of one RCT [669], [668] were available, but could not demonstrate a significant long-term effect.
The short-term effectiveness of psycho-oncological e-health interventions regarding anxiety was investigated in two meta-analyses [666], [667]. One of the meta-analyses demonstrated significant short-term effects in favor of psycho-oncological e-health interventions (d=-0.16). In addition, the results of 16 RCTs [670], [683], [685], [674], [686][687][688], [676], [677], [678], [679], [689], [690], [691], [692], [693] were available, four of which identified significant short-term effects in favor of psycho-oncological e-health interventions.
The medium-term effectiveness of psycho-oncological e-health interventions with regard to anxiety was not investigated in any systematic review. Only twelve RCTs were available [669], [668], [684], [685], [686], [687], [688], [676], [677], [678], [679] [690], [691], two of which were able to demonstrate significant medium-term effects in favor of psycho-oncological e-health interventions. One of the RCTs provided mixed results (significant effect regarding recurrence anxiety, but not regarding general anxiety).
No systematic reviews were available to assess the long-term effectiveness of psycho-oncology e-health interventions on anxiety. Only the results of two RCTs were available [669], [668], [684], one of which found mixed results regarding psycho-oncological e-health interventions (significant effect regarding recurrence anxiety, but not regarding general anxiety). The other RCT failed to identify a significant long-term effect.
The short-term efficacy of psycho-oncological e-health interventions with regard to fatigue was examined in two meta-analyses [665], [666], one of which demonstrated significant short-term effects in favor of psycho-oncological e-health interventions (d=-0.30). In addition, eight RCTs on the short-term efficacy of fatigue were available [675], [686], [687], [688], [676], [679], [680], [692], two of which found significant short-term effects in favor of psycho-oncological e-health interventions.
The medium-term efficacy of psycho-oncological e-health interventions on fatigue was not investigated in any systematic review. Only five RCTs were available [686], [687], [688], [676] [679], none of which found significant medium-term effects in favor of psycho-oncological e-health interventions.
Pain and sexual dysfunction (Statement 8.13)
The short- and medium-term efficacy of psycho-oncological e-health interventions on pain has only been investigated in two RCTs [686], [688], neither of which, however, was able to determine significant, short- and medium-term effects in favor of psycho-oncological e-health interventions.
The short-term effectiveness of psycho-oncological e-health interventions on sexual function was not investigated in any systematic review. Only four RCTs were available [672], [673], [678], [694], [695], [693], one of which was able to demonstrate a significant, short-term effect in favor of psycho-oncological e-health interventions.
The medium-term effectiveness of psycho-oncological e-health interventions regarding sexual function has not been investigated in any systematic review. Only the results of four RCTs were available [672], [678], [694][695], [681], none of which, however, could demonstrate a significant, medium-term effect in favor of psycho-oncological e-health interventions.
There were also no systematic reviews available for assessing the long-term effectiveness of psycho-oncological e-health interventions with respect to sexual function. In addition, the results of the two available RCTs [694], [695], [681], showed no significant long-term effects in favor of psycho-oncological e-health interventions.
The studies on the reduction of pain and sexual dysfunction are not sufficiently reliable. In particular, the RCTs on sexual function are very heterogeneous in terms of content; only two studies have a priori power analyses with a sufficient number of cases. Furthermore, none of the studies included makes statements on side effects and interactions of the interventions investigated. The guideline group therefore refrains from making a recommendation for or against the use of psycho-oncological e-health interventions for these complaints. Additional, methodologically high-quality studies are needed to formulate a recommendation.
Supporting evidence
In addition to the above results, the systematic review by Okuyama et al. [682] descriptively describes that in eight of 20 included RCTs, significant short-term effects in favor of psycho-oncological e-health interventions on at least one surveyed psychosocial endpoint (including quality of life, depressiveness, anxiety, mental distress, recurrence anxiety) was demonstrated. Furthermore, four RCTs in the review reported outcomes at follow-up time points, and one of these demonstrated significant effects in favor of psycho-oncology e-health interventions.
Assessment of study quality
All SRs (5/5; 100%) had deficiencies in more than one critical assessment domain (critical low quality).
In total, 21/28 RCTs (75%) used an adequate method to generate the randomization sequence (selection bias), 12/28 RCTs (43%) ensured secrecy and unpredictability of group allocation (selection bias), in 24/28 RCTs (86%), the amount of missing data was sufficiently small (<20%) or missing data were appropriately imputed (attrition bias), and in 8/28 RCTs (29%), selective reporting of endpoints could be excluded by an existing study protocol (reporting bias). Due to the nature of the interventions used and the collection of endpoints by self-assessment, blinding of study personnel/participants (performance bias) was not possible in any of the RCTs. In a large number of RCTs (n=23), blinding of the endpoint survey (detection bias) was not possible; in five RCTs, no statement could be made in this regard.
16/28 RCTs performed a priori case number planning, of which 12 RCTs achieved their a priori planned number of cases.
8.5 Psychotherapeutic Interventions
8.5.1 Psychotherapeutic Interventions in Individual and Group Settings
Psychotherapeutic interventions shall be offered to cancer patients with an adjustment disorder or subsyndromal distress in order to reduce psychological distress, depressiveness, anxiety, and nausea, as well as to improve quality of life.
- Recommendation grade
- A: Starke Empfehlung für oder gegen ein Maßnahme - verwendete Ausdrucksweise = soll/soll nicht
- Level of evidence
- 1a
- Consensus
- Strong consensus (100%)
- References
- [582] [583] [584] [585] [586] [587] [588] [589] [590] [591] [592] [593] [696] [697] [594] [595] [596] [598] [599] [600] [628] [601] [602] [603] [604] [605] [606] [607] [608] [609] [610] [611] [612] [613] [614] [615] [627] [616] [617] [618] [619] [620] [621] [623] [622] [624] [625] [626]
Change note
Individual psychotherapeutic interventions are to be offered to people with cancer and an adjustment disorder or subsyndromal distress. The somatic and social factors identified in the diagnostic process and their interactions are to be taken into account.Psychotherapeutic interventions can be offered to cancer patients with an adjustment disorder or subsyndromal distress in order to reduce pain as an adjunct to guideline-based pain management.
- Consensus
- Strong consensus (97,2%)
- References
- [582]
Systematic literature review
The evaluation of the effectiveness of psychotherapeutic interventions in cancer patients and survivors is based on 16 systematic reviews as well as 21 RCTs for individual psychotherapy, and 18 RCTs for group psychotherapy. One of these 39 RCTs was already included in one of the systematic reviews, therefore, the results of this study are not reported separately in the results.
The 16 systematic reviews (13 meta-analyses, three systematic reviews) included between six and 245 primary studies in the analysis. Regarding the tumor entities studied, seven reviews focused exclusively on breast cancer and one each on lung and prostate cancer. The remaining reviews (n=7) examined mixed cancer populations. The primary studies included were from the US, Asia, Australia, UK, and the EU, among others. Several reviews focused on only one endpoint: three meta-analyses reported exclusively on the efficacy of psychotherapeutic interventions for reducing depression [583], [591], [592], one for increasing quality of life [586], one for reducing anxiety [585], and one for reducing fatigue [631].
The sample size of the 21 RCTs that examined individual psychotherapy varied from 30 to 1012 patients (N=3,624), of whom 14.5-100% were female. The studies were mostly from the United States (n=3), Canada (n=2), Iran (n=2), China (n=2), and Germany (n=2). The remaining studies were from the Netherlands, Italy, Denmark, Turkey, Norway, Greece, New Zealand, Qatar, South Korea, and Brazil (n=1 each). Regarding the tumor entities investigated, eight studies focused exclusively on breast cancer, two on gynecologic cancers, and one study each on leukemia, esophageal cancer, colorectal cancer, head and neck cancer, and patients undergoing hematopoietic stem cell transplantation. The remaining studies (n=6) examined patients with various cancer diagnoses without focusing on a specific cancer type. Most individual psychotherapies were multimodal interventions with different components. Elements of psychosocial counseling (n=10), skills and management training (n=6), cognitive (-behavioral) elements (n=3), and problem-solving training (n=2) were frequently implemented. The number of intervention sessions presented ranged from one session to 35 sessions. Most frequently, depressiveness (n=10), quality of life (n=9), anxiety (n=8), and psychological distress (n=5) were collected as primary outcomes. Furthermore, pain (n=3), sexual function (n=2), nausea (n=1), and fatigue (n=1) represented primary endpoints in the RCTs.
The sample size of the 18 RCTs that investigated group psychotherapy varied from 25 to 392 patients (n=2,299), of whom 47-100% were female. The studies were mostly from the USA (n=4) and Iran (n=4), as well as China (n=3), Canada (n=2), China (n=2), and Germany (n=2). The remaining studies were from the Netherlands, Spain, and Brazil (n=1 each). Regarding the tumor entities investigated, 11 studies focused exclusively on breast cancer and one study on gynecologic cancer and breast cancer. Furthermore, one study each focused exclusively on lung cancer and prostate cancer, and one study on prostate cancer and gastrointestinal tumors. The remaining studies (n=3) examined patients* with different cancer diagnoses. In the group psychotherapies, cognitive-behavioral (n=4), social-supportive (n=3), and supportive-expressive and psychodynamic therapy elements (n=3) were most frequently used. The primary endpoints most frequently assessed in the RCTs represented depressiveness (n=7), anxiety (n=7), and quality of life (n=7). In addition, sexual function/satisfaction (n=2), psychological distress (n=1), and fatigue (n=1) were collected as primary endpoints.
Results
Of the 16 included reviews, only two differentiated between individual and group psychotherapy in the presentation of results [582], [593]. Therefore, the results of the systematic reviews are also reported below for psychotherapeutic interventions as a whole, i.e., not differentiated between individual and group therapy.
The results of the additionally searched RCTs are presented separately for individual psychotherapy and group psychotherapy.
Since no studies were available which directly compare psychotherapeutic interventions in individual versus group settings, Recommendation 8.1 was formulated in the guideline group on the basis of expert consensus. The choice between individual and group psychotherapy should be based on the patient's preference. However, since group offerings are not as common in the reality of care, the choice will essentially depend on which offerings are available locally.
Quality of life, psychological distress, depressiveness, anxiety, and nausea (Recommendation 8.14)
The short-term effectiveness of psychotherapeutic interventions on global quality of life has been examined in seven meta-analyses [584], [586], [588], [589], [590], [593], [582], all of which demonstrated a significant short-term effect in favor of psychotherapeutic interventions (0.09 ≤ d ≤ 0.65). In contrast, one systematic review [697] describes that only one of the six RCTs included in the review found a significant effect in favor of psychotherapeutic interventions. In addition, our research found ten RCTs on individual psychotherapy [597], [600], [604], [605], [607], [610], [595], [603], [609], [606] and eight RCTs on group psychotherapy [614], [618] [619], [616], [623], [622], [624], [617] which investigated short-term efficacy with regard to global quality of life. Of these, five RCTs on individual psychotherapy and one RCT on group psychotherapy were able to show a significant effect with regard to global quality of life.
The medium-term efficacy of psychotherapeutic interventions with respect to global quality of life was examined in three meta-analyses [588], [589], [582], two of which demonstrated a significant medium-term effect in favor of psychotherapeutic interventions (d = 0.15 and d = 0.38). In addition, our research found eight RCTs on individual psychotherapy [597], [604], [605], [610], [595], [603], [609], [606] and six RCTs on group psychotherapy [618], [619], [616], [622], [624], [617] which examined medium-term efficacy with respect to global quality of life. Three RCTs on individual psychotherapy and one RCT on group psychotherapy showed a significant effect on global quality of life.
The long-term efficacy of psychotherapeutic interventions regarding global quality of life was examined in two meta-analyses [589], [582] and could only be demonstrated in Faller et al. (d=0.37). In addition, our research found two RCTs on individual psychotherapy [597], [600] and three RCTs on group psychotherapy [618], [626], [616] that examined long-term efficacy with respect to global quality of life. None of the RCTs on individual psychotherapy and one RCT on group psychotherapy showed a significant effect on global quality of life. One RCT [618] on group psychotherapy described mixed findings (significant effects for 6 and 12 months, but not for 18 months).
The short-term efficacy of psychotherapeutic interventions regarding psychological distress was examined in four meta-analyses [584], [588], [590], [582], all of which demonstrated a significant short-term effect in favor of psychotherapeutic interventions (-0.23 ≤ d ≤ -0.48). Furthermore, three systematic reviews describe that two of two [593], one of two [696], and eight of 13 [697] RCTs included in the respective reviews found a significant, short-term effect in favor of psychotherapeutic interventions. In addition, our research found six RCTs on individual psychotherapy [596], [597], [610], [595], [608], [606] and five RCTs on group psychotherapy [611], [619], [612], [624], [617] which investigated the short-term efficacy regarding psychological distress. Two RCTs on individual psychotherapy and two RCTs on group psychotherapy showed a significant effect on psychological distress.
The medium-term effectiveness of psychotherapeutic interventions with regard to psychological distress was examined in two meta-analyses [588], [582], both of which demonstrated a significant medium-term effect in favor of psychotherapeutic interventions (d=-0.18 and d=-0.21). In addition, our research found six RCTs on individual psychotherapy [596], [597], [610], [595], [608], [606] and five RCTs on group psychotherapy [611], [619], [612], [624] which investigated the medium-term efficacy regarding psychological distress. Two RCTs on individual psychotherapy and two RCTs on group psychotherapy showed a significant effect on psychological distress. One RCT [619] on group psychotherapy showed mixed findings (significant effect after three months, but not after six months).
The long-term effectiveness of psychotherapeutic interventions on psychological distress was examined in one meta-analysis [582], which demonstrated a significant long-term effect in favor of psychotherapeutic interventions (d=-0.15). In addition, one RCT on individual psychotherapy [597] was available from our search that examined long-term efficacy with respect to psychological distress. No significant effect in favor of psychotherapy could be demonstrated.
The short-term efficacy of psychotherapeutic interventions regarding depressiveness has been examined in eight meta-analyses [583], [584], [588], [589], [591], [592], [593], [582], six of which demonstrated a significant short-term effect in favor of psychotherapeutic interventions (-0.25 ≤ d ≤ -1.11). Furthermore, one systematic review [696] describes that in four of six RCTs included in the review, a significant, short-term effect in favor of psychotherapeutic interventions was found. In addition, our search found 12 RCTs on individual psychotherapy [596], [597], [598], [599], [600], [628], [601], [604], [610], [594], [595], [609] and nine RCTs on group psychotherapy [611], [615], [627], [619], [620], [625], [612], [621], [622] which investigated short-term efficacy with regard to depression. Of these, seven RCTs on individual psychotherapy and five RCTs on group psychotherapy were able to show a significant effect with regard to depressiveness.
The medium-term efficacy of psychotherapeutic interventions with respect to depressiveness was examined in three meta-analyses [588], [589], [582], one of which demonstrated a significant medium-term effect in favor of psychotherapeutic interventions (d=-0.13 (individual), d=-0.21 (group)). In addition, our search found nine RCTs on individual psychotherapy [596], [597], [599], [628], [604], [610], [594], [595], [609] and seven RCTs on group psychotherapy [611], [615], [627], [619], [612], [621], [622] which examined medium-term efficacy with respect to depression. Of these, four RCTs on individual psychotherapy and three RCTs on group psychotherapy were able to show a significant effect with regard to depressiveness. One RCT [619] on group psychotherapy showed mixed findings (significant effect at three months but not at six months).
The long-term effectiveness of psychotherapeutic interventions with respect to depressiveness was examined in three meta-analyses [588], [589], [582], one of which demonstrated a significant long-term effect in favor of psychotherapeutic interventions (d=-0.28). In addition, our research found two RCTs on individual psychotherapy [600], [594] and two RCTs on group psychotherapy [626], [621] that examined long-term efficacy with respect to depression. One RCT on individual psychotherapy and one RCT on group psychotherapy showed a significant effect on depression.
The short-term effectiveness of psychotherapeutic interventions regarding anxiety was examined in seven meta-analyses [584], [585], [587], [588], [589], [593], [582], six of which demonstrated a significant short-term effect in favor of psychotherapeutic interventions (-0.21 ≤ d ≤ -1.1). Furthermore, one systematic review [696] describes that in two of the three RCTs included in the review, a significant short-term effect in favor of psychotherapeutic interventions was found. In addition, our search found nine RCTs on individual psychotherapy [596], [597], [598], [600], [604], [610], [594], [595], [602] and nine RCTs on group psychotherapy [611], [613], [615], [627], [619], [625], [621], [622], [617] that examined short-term efficacy with respect to anxiety. Three RCTs on individual psychotherapy and six RCTs on group psychotherapy showed a significant effect on anxiety. One RCT [598] on individual psychotherapy showed mixed findings (significant effect on HADS-A, but no significant effect on SAS).
The medium-term effectiveness of psychotherapeutic interventions on anxiety was examined in four meta-analyses [587], [588], [589], [582], two of which demonstrated a significant medium-term effect in favor of psychotherapeutic interventions (d=-0.19 and d=-0.33 (individual) and d=-0.22 (group), respectively). In addition, our search found six RCTs on individual psychotherapy [596], [597], [604], [610], [594], [595] and seven RCTs on group psychotherapy [611], [615], [627], [619], [621], [622], [617] which investigated the medium-term efficacy regarding anxiety. One RCT on individual psychotherapy and four RCTs on group psychotherapy showed a significant effect on anxiety. In one RCT on group psychotherapy [622] patients in the psychotherapy group experienced more anxiety than patients in the control group three months after the intervention.
The long-term efficacy of psychotherapeutic interventions with regard to anxiety was examined in two meta-analyses [589], [582], one of which demonstrated a significant long-term effect in favor of psychotherapeutic interventions (d=-0.46). In addition, our search found three RCTs on individual psychotherapy [597], [600], [594] and one RCT on group psychotherapy [621] which examined long-term efficacy with respect to anxiety. Only two RCTs on individual psychotherapy showed a significant long-term effect on anxiety.
The short-term effectiveness of psychotherapeutic interventions regarding nausea was investigated in one meta-analysis [588]. A significant short-term effect in favor of psychotherapeutic intervention was demonstrated (d=-0.39). In addition, our search found one RCT on individual psychotherapy [701] which investigated the short-term efficacy regarding nausea. A significant short-term effect in favor of psychotherapy was demonstrated.
Regarding the medium-term efficacy of psychotherapeutic interventions on nausea, only one RCT [701] on individual psychotherapy was available according to our research. A significant medium-term effect in favor of psychotherapy could be demonstrated.
According to our search, no studies on the long-term effectiveness of psychotherapeutic interventions regarding nausea were available.
Fatigue (Recommendation 8.15)
The short-term efficacy of psychotherapeutic interventions regarding fatigue has been examined in two meta-analyses [631], [588], one of which demonstrated a significant short-term effect in favor of psychotherapeutic interventions (d=-0.42⁶). Furthermore, two systematic reviews describe that in one of five [697] and two of two [698] RCTs included in the review, a significant short-term effect in favor of psychotherapeutic interventions was found. In addition, our search found three RCTs on individual psychotherapy [597], [604], [607] and two RCTs on group psychotherapy [702], [624] that examined short-term efficacy with respect to fatigue. Two RCTs on individual psychotherapy and one RCT on group psychotherapy showed a significant effect on fatigue.
The medium-term efficacy of psychotherapeutic interventions regarding fatigue was only investigated in one meta-analysis [588]. No significant medium-term effect in favor of psychotherapeutic intervention could be demonstrated. In addition, our search found two RCTs on individual psychotherapy [597], [604] and one RCT on group psychotherapy [624] which investigated the medium-term efficacy regarding fatigue. Only one RCT on individual psychotherapy showed a significant medium-term effect in favor of psychotherapy.
According to our search, only one RCT [597] on individual psychotherapy was available for the long-term efficacy of psychotherapeutic interventions with regard to fatigue. No significant effect in favor of individual psychotherapy could be demonstrated.
⁶ Effect only significant for patients after end of treatment, not significant for patients receiving treatment.
Pain (Recommendation 8.16)
The short-term effectiveness of psychotherapeutic interventions regarding pain was investigated in two meta-analyses [588], [589]. No significant short-term effect in favor of psychotherapeutic intervention was demonstrated in either of the two. However, one systematic review [697] describes that a significant short-term effect in favor of psychotherapy was demonstrated in four of the five RCTs included in the review. In addition, our search found four RCTs on individual psychotherapy [596], [604], [607], [603], which investigated short-term efficacy with regard to pain. Of these, only one RCT was able to show a significant effect with regard to pain.
The medium-term efficacy of psychotherapeutic interventions regarding pain was only investigated in one meta-analysis [589]. No significant medium-term effect in favor of psychotherapeutic intervention could be demonstrated. In addition, our search found three RCTs on individual psychotherapy [596], [604], [603] which investigated the medium-term effectiveness regarding pain. Only one RCT demonstrated a significant medium-term effect in favor of psychotherapy.
According to our research, no studies on the long-term efficacy of psychotherapeutic interventions regarding pain were available.
Sexual dysfunction (Statement 8.17)
No systematic reviews were available on the efficacy of psychotherapeutic interventions regarding sexual function, according to our search.
The short-term effectiveness of psychotherapeutic interventions regarding sexual function was examined in one RCT on individual psychotherapy [700] and two RCTs on group psychotherapy [616], [623]. Only the RCT on individual psychotherapy was able to demonstrate a significant short-term effect in favor of psychotherapy.
The medium-term effectiveness of psychotherapeutic interventions regarding sexual function was investigated in one RCT on individual psychotherapy [699] and one RCT on group psychotherapy [616]. Both RCTs were able to demonstrate a significant medium-term effect regarding sexual function.
The long-term effectiveness of psychotherapeutic interventions regarding sexual function was only examined in one RCT on group psychotherapy [616]. No significant long-term effect could be demonstrated.
The evidence base on the effectiveness of psychotherapeutic interventions to reduce sexual dysfunction in cancer patients is heterogeneous and not sufficiently robust. Sexual function was the primary outcome in all RCTs, and two of the four RCTs had a sufficiently large sample size after a priori power analysis. One RCT provided information on side effects and interactions, but these did not occur in either the control or the psychotherapy groups. The methodological quality of all RCTs is considered moderate to low. The guideline group therefore reserves the right to refrain from recommending for or against the use of psychotherapeutic interventions in cancer patients with these complaints. Further studies of high methodological quality are needed to formulate a recommendation.
Assessment of study quality
In total, 13/16 (81%) SRs had deficiencies in more than one critical assessment domain (critical low quality), 2/16 (13%) had deficiencies in one critical assessment domain (low quality), and one (6%) SR had no critical deficiencies and only one non-critical deficiency (high quality). It should be noted that 5/16 SRs had a downgraded quality assessment due to the lack of a list of excluded primary studies and their reasons for exclusion (critical domain 7, AMSTAR-2).
17/21 RCTs (81%) on individual psychotherapy used an adequate method to generate the randomization sequence (selection bias) and 9/21 RCTs (43%) ensured secrecy and unpredictability of group allocation (selection bias); in 11/21 RCTs (52%), the amount of missing data was sufficiently small (<20%) or missing data were appropriately imputed (attrition bias); and in 6/21 RCTs (29%), selective reporting of endpoints could be excluded by an existing study protocol (reporting bias). Due to the nature of the interventions used and the collection of endpoints by self-assessment, blinding of study personnel/participants (performance bias) and thus blinding of endpoint collection (detection bias) were not possible in any of the RCTs.
In total, 13/21 RCTs performed a priori sample size estimation. 6 RCTs achieved their a priori planned sample size.
13/18 RCTs (72%) on group psychotherapy used an adequate method to generate the randomization sequence (selection bias); 4/18 RCTs (22%) ensured secrecy and unpredictability of group allocation (selection bias); in 11/18 RCTs (61%) the amount of missing data was sufficiently small (<20%) or missing data were imputed accordingly (attrition bias). In 1/18 RCTs (6%), selective reporting of end points could be excluded by an existing study protocol (reporting bias). Due to the nature of the interventions used and the collection of endpoints by self-assessment, blinding of study personnel/participants (performance bias) and thus, with the exception of one RCT, blinding of endpoint collection (detection bias) was not possible in any of the RCTs.
In total, 8/18 RCTs performed a priori sample size estimation. 6 RCTs achieved their a priori planned sample size.
8.5.2 Psychotherapeutic Couple and Family Interventions
- Recommendation grade
- 0: offene Empfehlung (Option) bzgl. einer Maßnahme - verwendete Ausdrucksweise = kann
- Level of evidence
- 1a
- Consensus
- Strong consensus (97%)
- References
- [582] [703] [704] [705] [706] [707] [708] [709] [710] [711] [712]
Change note
Psychotherapeutic couple interventions are to be offered to people with cancer and an adjustment disorder or subsyndromal distress. The somatic and social factors identified in the diagnostic process and their interactions are to be taken into account.The evidence on the effectiveness of psychotherapeutic couple and family interventions in reducing pain, fatigue, and sexual dysfunction in cancer patients does not support a recommendation for or against their use for these conditions.
The inclusion of partners or relatives of cancer patients in the psycho-oncological treatment is a natural component of a bio-psycho-social treatment concept. This chapter focuses on specific psychotherapeutic couple and family interventions and their effectiveness in reducing mental and physical distress in people with cancer.
Systematic Literature Review
The evaluation of the effectiveness of couple and family interventions in cancer patients and survivors is based on seven systematic reviews and five RCTs. One of the five RCTs was already included in one of the systematic reviews, therefore, the results of this study are not reported separately in the results.
The seven systematic reviews (five meta-analyses, two systematic reviews) included between ten and 198 primary studies in the analysis. Six of the reviews examined mixed cancer populations and one paper specifically included breast cancer patients. The primary studies included were from the United States, Australia, Canada, Iran, and the EU, among other countries. One meta-analysis reported exclusively on the effectiveness of psychotherapeutic couple and family interventions for increasing quality of life [706]. All other reviews reported multiple relevant endpoints.
The sample size of the five RCTs varied from 17 to 237 patients (N=572), 0-100% were female. The studies were from Denmark (n=2), the USA, Australia, and the UK (n=1 each). In terms of tumor entities examined, three studies focused exclusively on prostate cancer, one study focused on breast cancer, and one study examined patients with multiple cancer diagnoses. Four studies examined couple-based treatment and counseling approaches, and one study examined a family coping intervention. The number of intervention sessions presented ranged from four to six sessions over a maximum period of five months. The primary endpoints collected by the RCTs were mental distress (n=3), quality of life (n=2), and depressiveness (n=1).
Results
Quality of life, mental distress, depressiveness, and anxiety (Recommendation 8.19)
The short-term effectiveness of psychotherapeutic couple and family interventions on global quality of life has been examined in four meta-analyses [703], [704], [706], [582], one of which demonstrated a significant short-term effect (d=0.25). In addition, Griffin and colleagues [707] described in detail in a systematic review that a significant effect in favor of couple and family interventions was not detectable in any of the six RCTs included in the review. In addition, the results of two RCTs were available from our search [709], [712], but they did not find a significant short-term effect in favor of psychotherapeutic couple and family interventions.
The medium-term effectiveness of psychotherapeutic couple and family interventions with regard to global quality of life was examined in three meta-analyses [703], [704], [582] and in two RCTs [709], [712]. Neither the meta-analyses nor the RCTs demonstrated significant medium-term effects in favor of psychotherapeutic couple and family interventions.
The long-term effectiveness of psychotherapeutic couple and family interventions with regard to global quality of life was also examined in three meta-analyses [703], [704], [582]. However, no significant long-term effect in favor of psychotherapeutic couple and family interventions could be demonstrated.
The short-term effectiveness of psychotherapeutic couple and family interventions on mental distress was examined in two meta-analyses [704], [582], one of which demonstrated a significant short-term effect in favor of psychotherapeutic couple and family interventions (d=-0.16). In addition, results of three RCTs [710], [711], [712] were available, but none of them could detect a significant short-term effect in favor of psychotherapeutic couple and family interventions.
Regarding the medium-term effectiveness of psychotherapeutic couple and family interventions with regard to mental distress, the results of two meta-analyses [704], [582] and three RCTs [710], [711], [712] were available. Neither the meta-analyses nor the RCTs demonstrated significant medium-term effects in favor of psychotherapeutic couple and family interventions.
The long-term effectiveness of psychotherapeutic couple and family interventions on psychological distress was examined in two meta-analyses [704], [582], none of which, however, demonstrated a significant effect in favor of psychotherapeutic couple and family interventions. No complementary RCTs were available.
The short-term efficacy of psychotherapeutic couple and family interventions with respect to depressivity was examined in four meta-analyses [703], [704], [705], [582], two of which demonstrated a significant short-term effect in favor of psychotherapeutic couple and family interventions (d=-0.26 and d=-2.15). In addition, one systematic review [707] descriptively describes that in two of nine included RCTs there was a significant effect in favor of psychotherapeutic couple and family interventions. In addition, the results of three RCTs [709], [710], [711] were available from our search, but none of them demonstrated a significant short-term effect in favor of psychotherapeutic couple and family interventions.
The medium-term efficacy of psychotherapeutic couple and family interventions on depressive symptoms was examined in three meta-analyses [703], [704], [582], two of which demonstrated a significant medium-term effect in favor of psychotherapeutic couple and family interventions (d=-0.29 and d=-0.37). In addition, the results of three RCTs were available [709], [710], [711], but they could not determine a significant medium-term effect in favor of psychotherapeutic couple and family interventions.
The long-term efficacy of psychotherapeutic couple and family interventions with regard to depressiveness was examined in two meta-analyses [704], [582] but they were unable to demonstrate a significant long-term effect in favor of psychotherapeutic couple and family interventions.
The short-term effectiveness of psychotherapeutic couple and family interventions regarding anxiety was examined in four meta-analyses [703], [704], [705], [582] two of which demonstrated a significant short-term effect in favor of psychotherapeutic couple and family interventions (d=-0.30 and d=-1.16). In addition, the result of one RCT [709] was available, but it did not find a significant short-term effect in favor of psychotherapeutic couple and family interventions.
The medium-term effectiveness of psychotherapeutic couple and family interventions with regard to anxiety was examined in a meta-analysis [704]. This demonstrated a significant medium-term effect in favor of psychotherapeutic couple and family interventions (d=-0.43). In addition, the results of one RCT [709] were available, but did not detect a significant, medium-term effect in favor of psychotherapeutic couple and family interventions.
The long-term effectiveness of psychotherapeutic couple and family interventions with regard to anxiety was examined in two meta-analyses [704], [582], one of which demonstrated a significant effect in favor of psychotherapeutic couple and family interventions (d=-0.26). No complementary RCTs were available.
Fatigue, pain, and sexual dysfunction (Recommendation 8.20)
Both the short- and medium-term efficacy of psychotherapeutic couple and family interventions on fatigue were examined only in the meta-analysis by Hu et al. [703]. However, no significant short- or medium-term effects in favor of psychotherapeutic couple and family interventions could be demonstrated. No complementary RCTs were available according to our search.
Both short- and medium-term efficacy of psychotherapeutic couple and family interventions on pain were also examined only in the meta-analysis by Hu et al. [703]. However, no significant short- or medium-term effects in favor of psychotherapeutic couple and family interventions could be demonstrated. No complementary RCTs were available according to our search.
Regarding sexual dysfunction, the systematic review by Brandao et al. [708] describes in detail that in eight of ten included RCTs, significant effects on at least one relevant outcome (psychological functioning level, physical functioning level, marital quality, sexual satisfaction) in favor of couple and family interventions were demonstrated. Four of these eight studies showed significant effects on sexual function/satisfaction in favor of the couple and family interventions.
No other systematic reviews or RCTs were available on this endpoint.
Assessment of study quality
All seven SRs (100%) had deficiencies in more than one critical assessment domain (critical low quality).
In total, 2/5 RCTs (40%) used an adequate method to generate the randomization sequence (selection bias), 3/5 RCTs (60%) ensured secrecy and unpredictability of group allocation (selection bias), in 2/5 RCTs (40%), the amount of missing data was sufficiently small (<20%) or missing data were appropriately imputed (attrition bias), and in 2/5 RCTs (40%), selective reporting of end points could be excluded by an existing study protocol (reporting bias). Due to the nature of the interventions used and the collection of endpoints by self-assessment, blinding of study personnel/participants (performance bias) and thus blinding of endpoint collection (detection bias) were not possible in any of the RCTs.
In total, 4/5 RCTs performed a priori case sample size estimation of which one RCT achieved their a priori planned sample size.
8.5.3 Specific Psycho-oncological Interventions in the Palliative Phase
The study data on the efficacy of specific psycho-oncological interventions in the palliative phase for reducing pain in people with non-curable cancer does not allow a recommendation for or against their use for these complaints.
Patients with a non-curable, progressive cancer are confronted with a variety of physical, mental, social and spiritual distress factors during the course of the disease [732]. Good palliative care therefore requires addressing the needs of patients in all four dimensions. It places the quality of life of patients with non-curable cancer at the center of its work (Extended S3 Guideline Palliative Care for Patients with Non-curable Cancer. Psycho-oncological interventions are part of a multi-professional and interdisciplinary palliative care approach. In this regard, we refer to the "Extended S3 Guideline on Palliative Care for Patients with Non-curable Cancer" (AWMF Registry Number:128-001OL, https://www.awmf.org/leitlinien/detail/ll/128-001OL.html).
Specific psycho-oncological interventions for patients in the palliative phase are usually supportive and focus to varying degrees on spiritual, psychological, physical or social aspects of cancer [733], [734]. Relaxation techniques, mindfulness-based interventions and meditation, therapeutic hypnotherapy elements, cognitive-behavioral therapy interventions, supportive-expressive interventions, and systemic family therapy approaches, as well as creative arts therapies may be used [732], [735]. In recent decades, specific interventions for working with palliative patients have also been developed and are briefly introduced below.
Meaning-Centered Psychotherapy is a form of existential psychotherapy developed by William S. Breitbart and colleagues that aims to find meaning and significance in the face of death [736], [737]. Originally conceptualized as a group therapy, Meaning-Centered Group Psychotherapy (MCGP) provides a framework in which (oncology) palliative care patients work together to address issues of meaning, inner peace, and goal orientation in life in the context of their illness [735]. Designed for eight sessions, seven main topics are worked on in a combination of psychoeducation, group discussions and exercises: 1. concepts of meaning and sources of meaning; 2. cancer and meaning; 3. creation of meaning from life history; 4. creation of meaning from the present and future; 5. creation of meaning from attitudes (encountering the limits of life); 6. creation of meaning from creative activity and taking responsibility; 7. experience-based creation of meaning (nature, art, humor) [738], [739]. In order to meet the needs of the palliative situation for flexibility of psychotherapeutic treatments, Individual Meaning-Centered Psychotherapy (IMCP), which works on the content of MCGP in seven individual sessions [740], [726], was also developed.
Managing Cancer and Living Meaningfully (CALM) therapy, developed by Gary Rodin and colleagues, is a manualized, semi-structured, short-term psychotherapeutic intervention in an individual setting [741], [742], [743], [723], [744]. In terms of content, CALM focuses on four areas: 1. symptom management and communication with treatment providers; 2. self-change and relationship with loved ones; 3. spirituality, meaning and significance; 4. preparing for the future, maintaining hope and coming to terms with dying [744].
Based on the empirical dignity model of Harvey M. Chochinov and colleagues, Dignity Therapy aims to alleviate patients' suffering at the end of life and improve their emotional and spiritual well-being [745], [746], [732]. In this process, patients are guided to reflect on memorable life events in an interview and 1-2 therapy sessions in an individual setting. The tape-recorded interview is then transcribed, read back to the patients, and edited if necessary. Patients are then given a document to leave with family members [732], [735]. The intervention is particularly aimed at patients in the terminal phase of their disease [732].
Systematic literature review
In this chapter, all psychotherapeutic interventions were considered that were explicitly directed at patients with non-curable cancer and addressed the physical, psychological, social and spiritual stresses of the palliative situation. The interventions were delivered exclusively in face-to-face contacts.
The evaluation of the effectiveness of psychotherapeutic interventions in the palliative phase is based on eight systematic reviews and 13 RCTs. One RCT [739] is already included in systematic reviews and is not reported separately in the results.
The eight systematic reviews (seven meta-analyses, one systematic review) included between eight and 68 primary studies in the analysis. All reviews included mixed cancer populations, other palliative populations were also included in three cases [714], [589], [715]. In these cases, the results reported below refer to subgroup analyses. The primary studies included were from the US, China, Canada, Australia, the UK, and the EU, among others.
The sample size of the 13 RCTs varied from 28 to 340 patients (N=1,926), 38.1-87.5% were female. The studies were from the USA (n=4), the Netherlands (n=2), Canada (n=2), the UK (n=2), Brazil, Nigeria, and Denmark (n=1 each). The majority of included studies (n=12) included patients with various advanced or terminal cancer diagnoses. One study was conducted with leukemia patients. Common interventions were meaning-based psychotherapy (IMCP/MCGP, CALM; n=3), elements of cognitive behavioral therapy (CBT; n=3), and psychoeducational elements (n=2). Two studies targeted couples. The number of intervention sessions ranged from a single session to 14 weekly sessions. Depressiveness (n=4) and quality of life (n=3) were most frequently collected as primary endpoints. Furthermore, fatigue, mental distress, and anxiety (n=1 each) were collected as primary endpoints.
Results
Quality of life, mental distress, depression, anxiety, and fatigue (Recommendation 8.21)
The short-term efficacy of specific psycho-oncological interventions in the palliative phase with respect to global quality of life was examined in six meta-analyses [713], [589], [715], [714], [716], [718], of which five demonstrated a significant short-term effect in favor of specific psycho-oncological interventions in the palliative phase (0.17 ≤ d ≤ 0.47). In addition, the results of seven RCTs were available [720], [723], [725], [726], [724], [730], [731], of which three found a significant short-term effect in favor of specific psycho-oncological interventions in the palliative phase.
The medium-term efficacy of specific psycho-oncological interventions in the palliative phase with respect to global quality of life was investigated in two meta-analyses [589], [718], one of which demonstrated a significant, medium-term effect in favor of specific psycho-oncological interventions in the palliative phase (d=0.82). In addition, the results of six RCTs [722], [723], [725], [726], [724], [731] were available, two of which recorded a significant medium-term effect in favor of specific psycho-oncological interventions in the palliative phase. In addition, one RCT [722] provided mixed results. No significant effect was shown at two, four, and eight weeks, but significant effect in favor of interventions in the palliative phase at 6 months was demonstrated.
The long-term effectiveness of specific psycho-oncological interventions in the palliative phase with regard to global quality of life was investigated in one meta-analysis [589] and in one RCT [731]. Within these studies, no significant long-term effects in favor of specific psycho-oncological interventions in the palliative phase could be demonstrated.
The short-term efficacy of specific psycho-oncological interventions in the palliative phase with regard to mental distress was investigated in four meta-analyses [713], [714], [716], [718], all of which demonstrated a significant, short-term effect in favor of specific psycho-oncological interventions in the palliative phase (-0.32 ≤ d ≤ -1.02⁷). In addition, results were available from five RCTs [725], [728], [724], [729], [730], two of which recorded a significant short-term effect in favor of specific psycho-oncological interventions in the palliative phase.
The medium-term effectiveness of specific psycho-oncological interventions in the palliative phase with regard to mental distress was investigated in a meta-analysis [718]. However, no significant medium-term effect in favor of specific psycho-oncological interventions in the palliative phase could be demonstrated. In addition, results of four RCTs [725], [727], [728], [724] were available, one of which demonstrated a significant, medium-term effect in favor of specific psycho-oncological interventions in the palliative phase.
The short-term efficacy of specific psycho-oncological interventions in the palliative phase with regard to depressiveness was investigated in five meta-analyses [713], [589], [715], [716], [718], four of which demonstrated significant, short-term effects in favor of specific psycho-oncological interventions in the palliative phase (-0.25 ≤ d ≤ -1.31) In addition, the results of six RCTs [721], [723], [726], [724], [729], [731] were available, two of which demonstrated significant short-term effects in favor of specific psycho-oncological interventions in the palliative phase.
Significant medium-term effects in favor of specific psycho-oncological interventions in the palliative phase were investigated in two meta-analyses [589], [718], none of which, however, demonstrated significant effects of specific psycho-oncological interventions in the palliative phase. In addition, results were available from six RCTs [721], [722], [723], [726], [724], [731], one of which demonstrated a significant effect in favor of specific psycho-oncological interventions in the palliative phase.
Long-term effects of specific psycho-oncological interventions in the palliative phase were investigated in one systematic review [589] and one RCT [731]. However, none of the studies found a significant long-term effect in favor of specific psycho-oncological interventions in the palliative phase.
The short-term efficacy of specific psycho-oncological interventions in the palliative phase with regard to anxiety was examined in five meta-analyses [713], [589], [715], [716], [718], four of which demonstrated significant short-term effects in favor of specific psycho-oncological interventions in the palliative phase (-0.21 ≤ d ≤ -1.07). In addition, results were available from five RCTs [723], [726], [728], [729], [731], two of which demonstrated significant short-term effects in favor of specific psycho-oncological interventions in the palliative phase.
The medium-term efficacy of specific psycho-oncological interventions in the palliative phase with regard to anxiety was examined in two meta-analyses [589], [718]. Neither could demonstrate significant effects of specific psycho-oncological interventions in the palliative phase. In addition, results from five RCTs [722], [723], [726], [728], [731] were available, two of which demonstrated significant effects of specific psycho-oncological interventions in the palliative phase.
Long-term effects of psychotherapeutic interventions in the palliative phase have been investigated in only one systematic review [589] and one RCT [731], both of which failed to identify significant effects.
The short-term efficacy of specific psycho-oncological interventions in the palliative phase with regard to fatigue was examined in two meta-analyses [714], [717], one of which demonstrated significant effects of specific psycho-oncological interventions in the palliative phase (d=-0.30). In addition, results from three RCTs [720], [727], [729] were available, two of which demonstrated significant short-term effects in favor of specific psycho-oncological interventions in the palliative phase.
The medium-term effectiveness of specific psycho-oncological interventions in the palliative phase with regard to fatigue was investigated in a meta-analysis [717]. This showed a significant effect in favor of specific psycho-oncological interventions in the palliative phase (d=-0.66).
The long-term efficacy of specific psycho-oncological interventions in the palliative phase with regard to fatigue was only investigated in one meta-analysis [717]. This could not find a significant effect of specific psycho-oncological interventions in the palliative phase. No supporting results from RCTs were available in our search.
⁷ In Li et al. (2020) [713] non-standardized MD=-7.3 in Patient Dignity Inventory [747].
Pain (Statement 8.22)
The short- and medium-term efficacy of specific psycho-oncological interventions in the palliative phase with regard to pain was examined in one meta-analysis [589], and one RCT [724].
The meta-analysis showed neither short nor medium-term effects of specific psycho-oncological interventions in the palliative phase, the RCT could only detect significant medium-term effects of specific psycho-oncological interventions in the palliative phase.
The study data on the effectiveness of specific psycho-oncological interventions in the palliative phase for the reduction of pain in people with non-curable cancer has to be considered as not sufficiently robust.
The meta-analysis by Bauereis et al. [589] includes only five RCTs that consider pain reduction as an outcome. The results have high unexplained heterogeneity, which reduces confidence in the effect estimator. The results on medium-term efficacy are based on only one RCT. Furthermore, the meta-analysis includes populations of cancer patients who are not in the palliative phase, thus decreasing the match to the key question of this chapter. The RCT by Rodin et al. [724] has only a small sample, and the planned sample size could not be achieved. Because of the limitations mentioned above, the guideline group refrains from recommending for or against the use of specific psycho-oncological interventions in the palliative phase to reduce pain in people with non-curable cancer. Additional methodologically high-quality studies are needed to formulate a recommendation.
Supplementary evidence
In addition to the above results, one systematic review [719] describes significant short-term effects on at least one primary endpoint (including quality of life, distress, pain) in 6/9 adequately powered RCTs of meaning-based interventions. In 5/9 RCTs with sufficient stat. Power on dignity-based interventions also showed significant short-term effects on at least one primary endpoint.
Assessment of study quality
The study quality of the SRs was assessed using the AMSTAR-2 tool, and the risk of bias of the RCTs was assessed using the Cochrane RoB tool.
In total, 5/8 (62.5%) SRs had deficiencies in more than one critical assessment domain (critical low quality), 2/8 (25%) had deficiencies in one critical assessment domain (low quality). One (12.5%) SR had no critical deficiencies and only one non-critical deficiency (high quality). It should be noted that in 4/8 SRs there was a downgrading of the quality assessment due to the lack of a list of excluded primary studies and their reasons for exclusion (critical domain 7, AMSTAR-2).
12/17 RCTs (70%) used an adequate method to generate the randomization sequence (selection bias), and 8/17 RCTs (47%) ensured secrecy and unpredictability of group allocation (selection bias). In 12/17 RCTs (70%), the amount of missing data was sufficiently small (<20%) or missing data were appropriately imputed (attrition bias), and in 8/17 RCTs (47%), selective reporting of endpoints could be excluded by an existing study protocol (reporting bias). Due to the nature of the interventions used and the collection of endpoints by self-assessment, blinding of study personnel/participants (performance bias) and thus blinding of endpoint collection(detection bias) were not possible in any of the RCTs.
In total, 10/13 RCTs performed a priori sample size estimation. 3/10 RCTs achieved their a priori planned sample size.
8.6 Psycho-oncological Crisis Intervention
Individuals with reduced coping resources, lack of social support, multiple somatic symptoms, additional stressors unrelated to illness, and previous traumatic experiences are at increased risk for acute crisis reactions.
- Consensus
- Consent (93%)
Psycho-oncological crisis intervention usually involves three phases: emotional relief, reflection on the cause of the crisis, and reintegration. If done promptly, it can prevent the development of subsequent psychological problems.
- Consensus
- Consent (82%)
Cancer patients and their relatives who show an acute crisis reaction shall be offered, regardless of care setting, psycho-oncological crisis intervention by psycho-oncologically trained specialists in a timely manner.
- Consensus
- Strong consensus (100%)
Controlled studies on the effectiveness of crisis intervention in the context of psycho-oncology are not yet available, as this form of intervention is difficult to standardize as emergency care. Therefore, no statements on the effectiveness of crisis intervention can be made here.
Crisis intervention plays a central role in the context of psycho-oncological practice. It differs from psychiatric crisis intervention in that it deals with psychological decompensation or suicidality in the context of mental disorders. Causes for crises in the oncological context can be: the existential shock and threat to the life perspective triggered by the diagnosis, loss of self-esteem due to functional impairments or amputations, massive side-effects from therapy or chronic problems resulting from therapy, the diagnosis of a recurrence or the determination of palliative stage of the disease, and many more. Secondary problems can also trigger crises such as increasing dependence, loss of control over one's own life, financial and social distress, conflicts in the family and work environment. Relatives can also experience an acute crisis, e.g. in case of extreme deterioration of the state of the disease, non-responsiveness of the patient or their own exhaustion in case of long-term illness [748], [123], [749], [750].
A crisis is a mental state of emergency, which can be defined as a loss of mental equilibrium triggered by confrontation with exceptionally threatening events or life circumstances that cannot be coped with at the moment because the individual's coping capacity is overwhelmed. Individuals with a high coping capacity are able to cope with high-level threats, whereas individuals with a low coping capacity experience a severe crisis reaction even in the face of low- or medium-level threatening situations. Relevant for the crisis experience is always the subjective significance of the triggering event, which should therefore not be downplayed by others.
In addition to minimal coping resources, a lack of social support, stress due to massive multiple physical symptoms, additional stressors unrelated to the illness and previous traumatic experiences can increase the vulnerability to crisis reactions.
An acute crisis reaction is characterized by fear, despair and the experience of powerlessness, hopelessness and excessive demands. In addition, impaired affect control and reduced cognitive functions (thinking, perceiving, decision-making) are typical symptoms. Appeals to clear thinking or reason therefore do not help. Crises are often accompanied by self-deprecating cognitions and suicidal fantasies [751].
In general, two patterns of crisis reactions can be distinguished, depending on whether affect flooding (excessive emotional reactions, „nervous breakdown“) or affect blockade (numbness, paralysis, apathy, „inner withdrawal“) occurs. The latter form, the „silent crisis“, is problematic because it is easily overlooked. The affected person then receives support too late, and possible suicidal thoughts cannot be addressed in time.
Psycho-oncological crisis intervention aims to mentally stabilize the affected person and to enable them to cope with the problematic (disease) situation on their own by supporting their coping skills and resources. The focus is entirely on the current situation. Psycho-oncological crisis intervention should take place as soon as possible due to the high level of suffering. In this manner, the chronification of the crisis reaction (protracted crisis) and the development of subsequent psychological problems can be prevented.
The procedure is based on three phases:
- Emotional relief: active listening fosters the acceptance of emotions; the therapist avoids trivializing, rationalizing, or hastily seeking solutions.
- Reflection on the cause of the crisis: After initial emotional stabilization has been achieved, the cause of the crisis can be reflected upon in its subjective meaning, and distortions of perception can be carefully corrected. Possible coping resources are brought into focus.
- Reintegration: The focus is now on regaining a sense of self-control and self-efficacy, promoting new perspectives and appreciating the coping skills that have been regained. The success of crisis intervention is demonstrated by the restoration of self-esteem and the ability to make decisions and take action. Further assistance (e.g. psychotherapy) can be planned.
Concomitant psychopharmacological medication can complement crisis intervention, but not replace it.
Suicidal fantasies are a symptom that often accompany crises of oncological patients [751] and can be understood as a plea or cry for help, or as an attempt to regain control over one's own life in fantasy. Such fantasies usually disappear when a therapeutic perspective for the cancer disease becomes apparent. In case of doubt, a psychiatric or psychosomatic specialist should be consulted to clarify acute suicidal tendencies.
8.7 Psychosocial Counseling
Psychosocial counseling in cancer counseling centers is an integrative intervention that can address psychological as well as social and socio-legal questions and problems.
- Consensus
- Consent (93%)
Psychosocial counseling with a psychological and social focus shall be offered to cancer patients and their relatives in all phases of the disease according to their needs and as early as possible.
- Consensus
- Strong consensus (98%)
Change note
Psychosocial counseling should be offered to cancer patients and their relatives in all phases of the disease, according to their needs and as early as possible.No RCTs are available for this section and, as a result, detailed information on effectiveness is not possible here. From the available observational studies, efficacy in the following areas is described for psychosocial counseling⁸:
- Reduction of psychosocial distress [752], [753], [754],[755],[756], [757]
- Reduction of occupational and financial difficulties and worries [758], [759], [760], [755]
- Improving emotional health [761],[762], reducing depression and/or anxiety [752],[753],[763], [764], [765],[766]
- Support in coping with illness [767] and improving quality of life [765],[768], [769], [770], [771], [772], [661], [773], [774]
- Improving couple/family relationships [763],[766],[775]
- Improvement of self-esteem [765]
- Reducing information deficits [752], [755], [770].
⁸ The term „social“ here refers to topics of social work which promotes integration in social life and participation in society, as well as access to social security programs.
Psychosocial counseling in the context of psycho-oncology is a professional communicative process between a psycho-oncological counseling specialist and a person seeking advice. Based on a needs assessment (anamnesis, stress screening, problem exploration related to the living environment), a problem and goal definition is developed together with the person seeking advice (counseling planning) and coping strategies are identified and developed. On the basis of a client-oriented approach, stabilization, problem-solving, relief and the activation of personal and social resources of those seeking advice are aimed for. Psychosocial counseling primarily serves to promote coping skills in dealing with illness-related psychosocial problems and stresses, and to facilitate access to government social assistance, which also includes referral to specialized facilities and other support services. Last but not least, the referral to regional self-help activities and opening doors to care structures play an important role.
Early counseling can also prevent the development or chronification of mental disorders. The target groups are not only those affected, but also relatives and people in the social environment [773].
Psychosocial counseling is offered in the outpatient setting primarily in psychosocial cancer counseling centers [123], [776]. In the inpatient setting, psychosocial counseling is also provided in acute care hospitals or rehabilitation clinics. Psychosocial counseling is usually the task of psychologists and social workers. Psychosocial counseling with a psychological focus can also be offered by physicians with psychotherapeutic qualifications. The counseling can relate to psychological distress and crises, as well as to social problems and questions about the use of social services. Depending on individual needs and the care setting (see Chapter 4.1.3 and 4.2), the focus may be more on social or psychological issues [123].
In the following, a distinction is therefore made between psychosocial counseling with a psychological focus and psychosocial counseling with a social focus. In cases where both topics are the subject of counseling, the competencies of both professional groups are to be included.
- Psychosocial counseling with a psychological focus relates primarily to psychological stress as a result of coping with the disease and adapting to the current disease and treatment situation[123], [777]. Examples are fears (existential threat, fear of the future, fear of progression), decision-making uncertainty, self-esteem problems, shame and guilt, depressive reactions, problems in the partnership and in dealing with children, psychological and physical long-term consequences of the therapy and thematic complex farewell/mourning/loss [777], [776]. The counseling is not based on psychopathological criteria, rather is open-ended and geared to the specific concerns of the person seeking advice. The main goals are psychological stabilization, the promotion of psychological coping and action skills, support in processing complex information and demads, and the dealing with existing inner-psychic conflicts. During the counseling process, the problem or conflict situation as well as various solutions and possible obstacles are analyzed together with the person seeking couseling, an individual solution to the problem is developed, which takes into account existing coping resources, and finally the implementation is monitored at later stages. The starting point is always the activation of existing personal and/or social resources.
- Psychosocial counseling with a social focus aims to clarify and support processes at the level of coping with everyday life and living, which can be made more difficult through the disruption of the psychosocial balance in the context of the disease and treatment [778], [779], [120]. Social integration and participation are also sought, which can be threatened in particular by barriers to staying or returning to work and by limited social and financial resources [780], [781], [782], [783]. In view of the complex problem situation, a wide range of other assistance is offered in addition to the communicative development of alternative perspectives and action strategies [118], [784], [755], [770], [769]:
- support in coping with everyday challenges and excessive demands as well as in communication with the social environment [785]
- information about social legal claims in case of illness and disability (e.g. rehabilitation, pension, reduction in earning capacity) and related assistance in applying for the respective benefits [787]
- advice on support options in the process of occupational reintegration [788]
- promoting self-determination and autonomy.
In addition, existential economic hardship, which, for example, can lead to loss of housing, problems providing for children and dependence on social benefits, represents a high potential for distress. Securing the socioeconomic basis and family care in cooperation with the responsible offices and authorities is central.
Psychosocial counseling should be offered according to need, as early as possible and in all phases [771] of the disease. The psychosocial burden and individual needs should be assessed in accordance with recommendations 7.1 – 7.3. The individual needs of those seeking advice should be determined via a systematic needs assessment and an assessment of the social care situation. If the presence of a mental disorder is suspected in the case of highly stressed persons seeking advice during psychosocial counseling, they should be referred to licensed psychotherapists or specialists for diagnostic clarification and further treatment (see Chapter 8.5).
Recommendations resulting from counseling and referrals should always take into account the patient's preference.
8.8 Creative Arts Therapies
Creative Arts Therapies (CAT) include art, music, dance and movement therapy, theater/drama therapy as well as poetry/bibliotherapy. Their methods are based on the therapeutic relationship and the interaction between patient, therapist and the creative-artistic medium or work. The goal of creative arts therapies is to regain, maintain and promote physical, mental and psychosocial health. Through the use of the tools and mediums offered by the arts, problems on social, emotional, cognitive, and physical levels can be addressed (BAG KT, 2019). Since the beginning of the 21st century, the use of artistic disciplines has played an increasingly important role in the field of prevention, in the promotion of health and in relation to the management and treatment of diseases and in rehabilitation [789]. The study “What is the Evidence on the Role of the Arts in Improving Health and Well-being? A "Scoping Review"” published in 2019 by the WHO [789] summarizes the evidence on the role of the arts in promoting health and overall well-being based on over 900 studies (200 reviews and more than 3,000 individual studies). Based on this work, the WHO recommends the use of the arts to enhance well-being as well as to promote and maintain health.
The field of oncology has also seen a steady increase in high-quality scientific research on the effectiveness of the arts therapies in recent decades. The Working Group on Creative Arts Therapies⁹ therefore conducted a systematic literature search on the efficacy of artistic therapies in adult cancer patients for the period 2012 to 2020 in the PRIMO library portal of the FU Berlin (https://fu-berlin.primo.exlibrisgroup.com/discovery/search?vid=49KOBV_FUB:FUB, last accessed on 31.03.2022). Further details can be found in the Guideline Report.
There were 58 level 1 studies for art, music, and dance and movement therapy according to the Oxford Levels of Evidence grading system, March 2009 version.
The following sections first report on studies focusing on the subdisciplines of CAT (art therapy, music therapy, dance and movement therapy), each with a LoE recommendation grading. Thereafter, studies (reviews) are reported in which more than one form of CAT has been investigated.
The evidence base (Level 1) for art therapy, music therapy, and dance therapy is summarized separately by subdiscipline on the basis of the reviews as well as the primary studies. Individual primary studies are also included in various reviews of art, music, and dance therapy from the survey period 2012-2020 and are therefore reported more than once.
⁹The working group creative arts therapies was supported by Pauline Thielen, Johanna Jost, Maria Guelguisser, Olivia Straeter, Lily Martin, Nilufar Yesmin, Seoyung Ryu, Daniel Narcisso, André Gianopoulos and Sophia Estel.
8.8.1 Art Therapy
Art therapy can be offered to cancer patients in order to reduce anxiety, depression and stress.
- Recommendation grade
- 0: offene Empfehlung (Option) bzgl. einer Maßnahme - verwendete Ausdrucksweise = kann
- Level of evidence
- 1a
- Consensus
- Consent (86%)
- References
- [790] [791] [792] [701] [793] [794] [795] [796] [797] [798] [799]
Change note
Artistic therapies (art therapy, dance therapy, music therapy, etc.) can be offered to people with cancer regardless of the level of stress.According to the definition of the Scientific Association for Creative Arts Therapies (WFKT), art therapy is the therapeutic application of artistic tools and media (painting, sculpture, photography, performance, etc.). It promotes in particular the skills of pictorial symbolic expression, visual communication, and an active creative exploration of personal issues and problems.
Four new systematic reviews have been found for art therapy since 2012 [791], [795], [701], [799]. These included were a total of eight randomized trials and ten controlled trials from 2006 to 2019. Three of the primary studies (RCTs) included in the reviews [797], [798], [790] are also reported individually, since they were published in the 2012-2020 search period. The studies were from the United States, Asia, and Europe. With the exception of the studies from Monti et al. (N=184) [797] and Joly et al. (N=320) [796], they are based on smaller numbers of cases (n<60). The applied art therapy methods and also the duration of the interventions are heterogeneous in the various studies. One review [799], for example, compared mindfulness-based art therapy (MBAT) with other mindfulness-based therapy approaches (such as Mindfulness Based Stress Reduction (MBSR) and Mindfulness Based Cognitive Therapy (MBCT) and also included individual studies from the field of palliative care [701].
A review by Wood et al. [800] has already shown that art therapy is helpful for people with cancer in various treatment settings. The art therapy approach can help to cope with treatment-related symptoms and support the process of psychological readjustment to the loss, change, and uncertainty caused by cancer. Art therapy is now often offered in group settings, and less frequently in individual therapy sessions. Supportive techniques are often used, for example, to regulate emotions, to experience relaxation through artistic expression, or, increasingly in mindfulness-based interventions.
Meta-analyses and systematic reviews
With regard to depressiveness, anxiety, and distress (mental illness domain), significant improvements with small to medium effects are found in various reviews ([791], [795], [799]. For example, Zhang [799] found significant improvement (p<.001) in depression scores as well as anxiety scores (p= .005) in 7 RCTs (n=888). Two reviews [791], [795] demonstrated significant improvements in quality of life (p<.01, d= 0.03-1.05). The review by Kim et al. [701], however, showed mixed results regarding quality of life, whereas five RCTs showed significant improvements in quality of life. Pain was examined by Kim et al. [701] in their review and came to different conclusions regarding an improvement in pain in the individual studies. A significant improvement of fatigue was described by Jiang et al. [795] in their review in four studies (p=.01). Furthermore, coping strategies were investigated in the review by Azmawati et al. [791], but no significant improvements could be shown.
Primary studies
An RCT by Joly et al. [796] examined an intervention group with art therapy in addition to standard care compared to a control group (treatment as usual, TAU) during radiation therapy. There were significant improvements in the areas of social well-being and cognitive fatigue. Monti et al. [797] and Jang et al. [794] were also able to demonstrate a significant improvement in quality of life after 36 months (p=.01). Öster et al. [798] found mixed results in the various domains investigating quality of life.
The investigations of the domain „Mental Illness“ showed heterogeneous results in the studies examined [790], [792], [797]. The study by Radl et al. [790] showed no significant improvements on emotional distress (p=.26) and mental well-being (p=.12), but did find significant improvement on spiritual well-being (p=.02). In contrast, the study by Jalambadi et al. [793] showed significant improvement on the different levels of distress (p<.05). The study by Jang et al. [794] measured significant improvement on depressiveness (p<.001) as well as anxiety (p<.001).
For improvement in coping, a recent RCT by Czamanski et al. [792] found significant improvements in emotion perception (p=.027) and emotion acceptance (p=.039), which was similarly demonstrated by Öster et al. [798] in the significant improvement in coping strategy of “social relationships” (p=.04). A significant improvement in fatigue is described by Joly et al. (p=.007) [796]. However, the result here refers only to patients with mild fatigue and not to patients with “severe fatigue” within the one-month study period. Three RCTs are also included in the reviews by Azmawati et al. [791], Jiang et al. [795] and Zhang et al. [799].
Risk of Bias Assessment
The risk of bias assessment of the 7 RCTs for art therapy was conducted by three independent raters (two non-specialist research assistants from medicine and psychology, and one specialist from music therapy; supervised by the Guideline working group CAT (KüTh)) using the RoB 2 tool [801]. In summary, a low risk of bias was found in three primary studies and a high risk of bias in four primary studies. The assessment took place with respect to five categories. The high Risk of Bias was found exclusively in Category 3 “bias due to missing outcome data”, i.e. due to missing data in the post test. The underlying drop-out of more than 20% of the patients is mostly explained clinically by the stressful oncological treatment with complex side effects and changes in life circumstances (relocations, etc.). The missing data was handled with appropriate methods in all four cases (intention-to-treat analysis, etc.). With the exception of these four cases, the methodological quality was homogeneous and high, with a low risk of bias.
Conclusion
Art therapy interventions show significant effects on the improvement of depressiveness, anxiety and distress; likewise from four studies to date for improvement of fatigue. The results of other outcome parameters examined, such as quality of life, coping strategies, pain reduction, and spiritual well-being, are heterogeneous. In addition, the duration of intervention and the type of art therapy interventions varied widely. The study data is characterized by strongly converging evidence of art therapy findings on the four outcomes mentioned above. With the exception of a drop-out rate of over 20% in four primary studies, the risk of bias assessment shows a high quality in the new primary studies (2012-2020).
8.8.2 Music Therapy
Music therapy should be offered to cancer patients to reduce anxiety, depression, stress, and improve health-related quality of life.
- Recommendation grade
- B: Empfehlung für oder gegen eine Maßnahme - verwendete Ausdrucksweise = sollte/sollte nicht
- Level of evidence
- 1a
- Consensus
- Consent (83%)
- References
- [802] [803] [804] [805] [806] [807] [808] [809] [810] [811] [812] [813] [814] [815] [816] [817] [818] [819] [820] [821] [822] [823] [824] [825] [826] [827] [828] [829] [830] [831] [832] [833] [834]
Change note
Music therapy can be offered to people with cancer, especially to reduce anxiety.Music therapy can be offered to cancer patients to reduce pain as an adjunct to guideline-based pain management.
Music therapy (MT) is „(…) the targeted use of music within the framework of the therapeutic relationship to restore, maintain and promote mental, physical and spiritual health“ [835]. Various music therapy concepts and methods (Neurological MT by M. Thaut; Guided Imagery and Music by Helen Bonny a.o.) are grouped under this heading and can basically be assigned to the following two approaches: Functional MT - for the treatment of primarily physiological complaints and Psychotherapeutic MT – with predominantly psychological treatment goals. The latter makes use of active methods (playing an instrument, singing, songwriting, etc.) and receptive methods (listening to individualized music, musical relaxation interventions, sound journeys, etc.), in which different mechanisms of action, both of the music as well as the therapeutic relationship, can be used. MT sessions can take place in individual and/or group settings, depending on the treatment goal and approach.
Music medicine (MM) refers to the use of music as a therapeutic tool by individuals without therapeutic training and outside of a therapeutic relationship (e.g., medical staff handing out an MP3 player/playlist to patients). Studies on music medicine were not included in the systematic literature search but are reported in some of the reviews that were included.
In the period from 2012 to 06/2020, a total of seven systematic reviews with meta-analyses on the use of music (therapy) and its influence on psychological and physiological parameters in cancer patients were published [803], [804], [802], [805], [806], [807], [808]. In addition, 25 new primary studies on oncological patients (excluding palliative patients) with a LoE 1 are available.
Meta-analyses and systematic reviews
The effect of music-based interventions on reducing anxiety is described as significant in six reviews. Bradt et al. [802] showed significant improvements in anxiety on the IGs compared to CG in 13 RCTs (N=1,028, significant improvements IGs vs. TAU; SMD = -0.71, 95% CI: -0.98; -0.43, p<.001) with a moderate to large effect. Zhang et al. [803] found a significant improvement on anxiety across different measurement tools (7 RCTs, N=607, SAS: M = −2.84, 95% CI:−19.51;−6.17, p<.001; 2 RCTs, N=515, HAMA: M=−1.85, 95% CI: -3.43;-0.27, p<.05; 8 RCTs, N=681, STAI: M=-12.30, 95% CI: -18.93;-5.68, p<.001) with small to moderate effect sizes. Li et al. [808] showed significant improvement on anxiety in the IG compared to CG on the basis of six RCTs (6 RCTs, N=447, SMD = −1.51, 95% CI: −2.27;0.75; p<.05), Gao et al. [805] based on three RCTs (N=121, SMD=0.68, 95% CI: 1.35;0.02; p=.04) and Wang et al. [806], in four RCTs (Anxiety: 2 RCTs, N=200, HAMA: MD= –7.04, 95% CI: –9.31;–4.78, p<.00001; 5 RCTs, N=268; SAS: MD=–7.40, 95% CI: -10.28;-4.52, p<.001; 2 RCTs, N=110, State Anxiety Inventory: MD=-12.40, 95% CI: -21.86;-2.94, p=.01). In their systematic review, Nightingale et al. [804] found a significant anxiety reduction in the IG compared to the CG in 85% (11/13) of the studies included: in the meta-analysis of 4 of the 13 included studies, no significant difference between the IG and the CG with regard to anxiety was found.
The effect of music-based interventions on reducing depressive symptoms is largely described as significant in five reviews. Wang et al. [806] were able to show a significant effect on depressivity based on the results of 14 studies from MT and MM (6 RCTs in MT, MD=-7.39, 95% CI: -8.35;-6.43, p<.001). Similarly, Zhang et al. [803] (7 RCTs, M=-6.23, 95% CI: -8.85; -3.36; p<.001) and Li et al. [808] (6 RCTs, SMD=-1.12, 95% CI: -1.87;-0.38, p<.05) showed significant results with regard to depressivity. In the Cochrane review by Bradt et al. [802], a short-term, moderate reduction in depressiveness through active music therapy interventions (SMD= -0.40, 95% CI: -0.74;-0.06, p<.02) was described. In their meta-analysis, Köhler et al. [807] found a significant improvement in mental well-being, reaching across aspects of anxiety, depressiveness, mental distress and well-being, mood, emotional functionality, relaxation, hope, and resilience in the IG (active MT) versus CGs (TAU, waiting list, and active CG: listening to music, visiting, mindfulness practice) (19 RCTs, d=0.35, 95% CI: 0.19;0.50, p<.01). It was found that a lower number of sessions had greater effects (d=0.47) than more frequent sessions (d=0.18). There were also greater effects with receptive MT (d=0.33) than with active or multimodal methods (d=0.19). In addition, a positive effect on depressiveness as well as mood was found. A significant improvement of physiological distress with small effect (physiol. distress: d=-0.34, 95% CI: -0.55;-0.13, p<.004) was also described. Gao et al. [805] were able to show a significant reduction in depressiveness in their review (4 RCTs, N=227, SMD: 1.08, 95% CI: 1.64;0.53, p<.001). Here, no significant improvement in social functioning was found (3 RCTs, SMD=0.51, 95% CI: 0.17;1.19, p=.14).
For improvement in quality of life, a significant effect was found in five reviews. The Cochrane Review by Bradt et al. [802] showed a significant increase in quality of life, also comparing MT versus MM, with moderate effects in three studies (SMD=0.42, 95% CI: 0.06;0.78, p=.02). Gao et al. [805] were able to find significant improvement on health-related quality of life in five studies (SMD=0.61, 95% CI: 0.41;0.82, p<.001). Köhler et al. [807] described a significant improvement with a small effect in their review on quality of life (d=0.48, 95% CI: 0.11;0.85, p=.019), although no significant effect was found for session frequency. Similarly, Li et al. [808] (10 RCTs, SMD: 0.54; 95% CI: 0.40;0.69; p<0.05) and Zhang et al. [803] (2 RCTs, M=13.32, 95% CI: 11.01;15.62, p<.001) described a significant effect for the improvement on different facets of quality of life.
Four out of five reviews could demonstrate a significant reduction in pain. Thus, Bradt et al. [802] (SMD: -0.91; 95% CI: -1.46;-0.36; p=.001), Li et al. [808] (SMD: -1.12; 95% CI: -1.87;-0.38; p<.05), Zhang et al. [803] (M:-0.54; 95%CI: -0.88; -0.20; p<.005), and Gao et al. [805] could determine a significant effect from MT on various parameters of pain. In addition, the review by Köhler et al. [807] described a positive effect on pain.
Inconsistent results regarding the significance on fatigue are found in three reviews. In the review by Bradt et al. [802], small to moderate improvements in fatigue were demonstrated in six studies with small to moderate effects (SMD: -0.38; 95% CI: -0.72;-0.04; p=.03). Zhang et al. [803] also report significant results on fatigue (2 RCTs, M: 0.63; 95% CI: -2.52; 3.77; p=.70). In the review by Gao et al. [805], no significant differences were found between intervention and control groups for fatigue (2 RCTs, SMD: 0.17, 95% CI: 0.95;0.61, p=.67).
Primary studies¹⁰
Twenty-two primary studies were included in the analysis. Individual RCTs are already included in one or more of the reviews and meta-analyses described above. Since the overlapping studies also include older primary studies prior to the designated search period, only the evidence from RCTs after 2014 will be presented separately below.
Music therapy significantly reduced anxiety in the majority of available studies. In the study by Palmer et al. [822] with inpatient breast cancer patients (N=201), the applications of listening to music pre- and perioperatively were compared live vs. recorded music compared to TAU. Anxiety was significantly reduced in both music IGs compared to TAU (MD: -26.5; d=-0.57; MD: -25.7; d=-0.55). By Romito et al. [826], anxiety was significantly improved in both the IG as well as the CG (d=0.69; p=.000). Wang et al. [806] (HAMA: p<.001; SAS: p<.001; State Anxiety Inventory: p=.01) as well as Yates and Silverman [833] (p=.009) each found significant improvement on anxiety in the IGs. Rossetti et al. [828], found a reduction in anxietythrough MT (10 sessions à 35 minutes listening to music with therapist, before and during treatment) during radiation treatment in gynecologic patients (MD: 8.2; p=.002). Dóro et al. [814], found significant group differences with regard to anxiety (IG vs EK: p<.001), whereas Bradt et al. [812] failed to find a significant effect with regard to anxiety (SMD: 0.21; 95% CI: -0.09;0.51, p=.18).
A significant reduction in depressiveness in the IG compared to the CG was demonstrated in the study by Alcântara-Silva et al. (p=.011) [809], as well as in Chen et al. [836]. Romito et al. [826] investigated the use of one session of integrative group MT (N=31) à two and a half hours concomitant with outpatient chemotherapy in 62 patients with breast cancer. Twenty-minute talks (N=31) were used as a control group. The MT group showed significant improvements for depressiveness (d=0.52; p=.000) and anger (d=0.58; p=.000). With regard to negative affect (SMD: -2.86; p=.003) and positive affect (SMD: 2.15; p=.001), the IG achieved greater improvements than the CG in the studies by Fredenburg and Silverman [815], [816].
With regard to hope and helplessness, two studies showed improvements. According to research by Chen et al. [836], the use of music-imagery in eight sessions à 60 minutes led to a reduction in helplessness and hopelessness, as well as cognitive improvement in 52 patients with breast cancer compared TAU. A study by Verstegen et al. [831] compared MT with therapeutic dialogue versus TAU in 10 patients with blood and bone marrow transplantation. The two sessions lasted between 30 and 60 minutes. The parameter hope was significantly improved here in the IG as well (post-test: p=.035).
The parameter stress improved significantly in the study by Romito et al. (IG: d=0.62; p=.036) [826]. Rossetti et al. [828] showed a reduction of distress through MT (IG: p=.0064). Regarding symptom-related physical stress, Fredenburg and Silverman [815], [816] found no significant difference between the intervention and waitlist groups.
Regarding quality of life, a study by Bieligmeyer et al. [811] showed significantly lower scores after MT intervention (single session à 10 minutes of vibroacoustic-combination of auditory and sensory sound experiences) compared to the CG (quiet time) (d=0.37; p<.001). A study by Alcântara-Silva et al. [809] showed a greater improvement in quality of life when listening to music together with a therapist before and after radiation therapy for gynecological oncology patients (N=164; 10 sessions of 35 minutes each) compared with TAU (p=.005). In a prospective palliative study by Warth et al. [832], 2 sessions of MT (30 min each at least 2 days apart) vs. MBSR were compared. With regard to quality of life, the authors found no significant group differences between intervention and control groups for the total quality of life scale in the pre-post comparison (F[1;81]=2.23, p=.14, MD= 3.26 [95%, CI: -5.99/ 12.5], η2=.03, SMD=.14 NNT=7). Ratcliff et al. (2014) [824] compared two different MT formats (ISO principle-based vs unstructured music (UM); 4 sessions each à 50 minutes) vs. TAU in patients after stem cell transplantation and found significant group differences in quality of life improvement comparing baseline to follow-up (p=.001) in favor of ISO principle-based MT (MT > UM > TAU).
The investigation of pain showed improvements in the IG, but no significant effect in the group comparison [811], [812], [814], [818], [831]. Bates et al. [810] examined the effect of two MT sessions à 30 minutes for a total of seven days on patients with multiple melanomas or lymphomas during their first stem cell therapy. Compared to the CG (TAU), there was no significant group difference regarding pain at any time (p=.73). The use of analgesics was not significantly different between IG and CG (p=.73), but it significantly increased in both groups at follow-up measurement (p=.001). Tuinmann et al. [830] investigated the effect of playing music, singing and listening to music in 66 lymphoma patients over eight sessions à 20 minutes versus TAU. They were able to demonstrate that the need for analgesics and the subjective pain perception were lower in the EG than in the CG (SMD: 10; 95% CI: 1.2;18.9; p=.027). Wang et al. [806] investigated the effect of perioperative music relaxation and postoperative music listening in five sessions à 60 minutes in 60 patients with lung cancer. The control conditions were TAU. The effect shown for the EG was a greater reduction in the need for analgesics. In 200 patients with advanced-stage cancer, Gutgsell et al. [817] found greater reduction in pain after a 20-minute session of music relaxation than in the wait-list CG (MD: -1.39; 95% CI: -1.95;0.83; p<.001). In two studies on blood and bone marrow patients [816], [815], Fredenburg and Silverman examined the effect of music therapy (various techniques) in one session à 30-45 minutes. Regarding pain, a greater decrease was demonstrated in the IG (SMD: -2.86; p=.009). Letwin and Silverman [818], examined 15 patients with different oncological diagnoses (oncology/hematology department) before and after two sessions of music listening à 30-45 minutes. Compared to the waiting-list CG, no significant differences in pain (p=.891) and resilience (p=.079) were demonstrated. In a study by Palmer et al. [822], no reduction in the need for anesthetics was seen with MT compared to the CG (LM vs. CG: MD:-3.3; 95% CI: -19.0;12.4; d=-0.09; RM vs. CG: MD: -8.6; 95% CI: -20.8;3.5; d:-0.24). Warth et al. [832] also found no significant group difference in pain perception between IG vs. the CG (F[1;81]=.40, p=.53, MD= -.18 [95%, CI:0.74/ 0.39], η2=.01, SMD=-.15 NNT=8.40). In contrast, Ratcliff et al. [824] described significant group differences in terms of improvement in cancer-related symptoms (such as pain, nausea, etc.) in the comparison between baseline to follow-up (p=0.01) in favor of ISO principle-based MT.
No improvement in fatigue was found by Fredenburg and Silverman (p>.05) [815]. However, Alcântara-Silva et al. [809] observed a significant reduction in fatigue in the IG compared to the CG (p=.01). In the study by Warth et al. [832], the authors demonstrated significant improvements in fatigue in favor of the IG vs. the CG (F[1;81]=4.74, p=.03).
The study results on the outcome mood are heterogeneous. The study by Bieligmeyer et al. [811] showed significant effects for current mood (d=0.43; p<.001) as well as for mood and well-being (p=0.47; p<.01), whereas no improvements were found in the CG. Especially the subscales of the BMQ used for inner balance (d=0.73; p<.001), vitality (d=0.51; p<.001) and alertness (d=0.37; p<.001) achieved significant improvements for the IG. Further significance in favor of the IGs was shown for the parameter satisfaction (d=0.43; p<.001). Palmer et al. [822] could not observe any improvement in satisfaction as a result of the live music intervention. In a study by Dóro et al. [814], stem cell therapy patients (N=100) were examined. Here, singing and musical Improvisation took place in eight sessions à 30 minutes. The CG received TAU. Mood improved in the IG more than in the CG (p<.001). Bradt et al. [812] offered music therapy employing different therapeutic techniques versus music listening as an active CG to inpatients and outpatients with different cancer diagnoses (N=31). Two sessions à 20-45 minutes did not lead to any significant group differences with regard to mood (MT: p<.0001 MM: p>.0001). Bates et al. [810] also found no significant group differences in the measurement of mood. Ratcliff et al. [824] showed significant improvement in mood after stem cell transplantation over four sessions of MT for both MT groups (p<.0001), with no significant difference detectable between the different MT interventions. Warth et al. [832] also described a significant improvement in the mood of palliative patients in the IG vs CG (F[1;81]=6.41, p=.01, MD= .98 [95%, CI: 0.28/ 1.68], η2=.61, SMD=.61 NNT=5.25).
Improved spiritual well-being in the IG compared to the CG was found by Cook and Silverman [813] (subscales: Hope: MD: 3.856; p=.011; Peace: MD: 2.194; p=.018; Meaning: MD:0.416; p=.677). They described the use of listening to music listening versus talking for 34 hematologic oncology patients (leukemia and other diagnoses). In three sessions à 15-30 minutes, the IG was compared with a waiting list CG.
Lin et al. [820] were able to show an improvement in relaxation with MT compared to TAU. Yates and Silverman [833] implemented one session of music listening à 20-30 minutes in 26 inpatients with colon, rectal, or uterine cancer. Compared to the waiting list group, increased relaxation was achieved in the experimental conditions (p=.009). Warth et al. [832] were also able to demonstrate a significant improvement in relaxation in favor of the IG vs. CG (F[1;81]=13.7, p<.01, MD=1.19 [CI: 0.50;1.88], η2=.75, SMD=.75, NNT=2.80) in a pre-post comparison after two 30-minute sessions of MT in palliative patients. Bradt et al. [812] did not find significant group differences with regard to anxiety (MT: p=.0002; MM: p<.0001).
For postoperative recovery time, Palmer et al. [822] showed significant results for live music compared to the use of recorded music (p=.018), but not compared to the TAU group. For 86 cancer patients (with various diagnoses) in outpatient treatment, Burns et al. [837] found improved responsiveness and post-traumatic growth (benefit finding/increased resilience) in a single session (45-50 min) with guided visualization with music compared to decreasing scores in the CG.
When examining physiological outcomes, the study by Bates et al. [810] showed no significant effect in regard to nausea. In the follow-up survey, the CG performed significantly better (p=.035). Moradian et al. [821], used active listening with the Nevasic audio program (pre-recorded audio program) during chemotherapy to reduce treatment-related nausea and vomiting in breast cancer patients (N=99). Listening to music in one group and TAU in another group were used as CGs. No group-specific differences were found with regard to nausea and vomiting. In the IG, the use of antiemetics significantly decreased compared to both CGs (p=.003). Warth et al. [832] found in their study in the palliative setting a significantly greater increase in the high-frequency component of heart rate variability in favor of the IG vs. CG (F [1;81]=8.13, p=.01, MD= .44 [95%, CI: 0.12/.77], η2=.09, SMD=.59 NNT=3.50). When blood volume and –amplitude were examined, only a trend toward vasodilation in favor of the IG vs. CG (F(1;81)=3.33, p=.07, MD= .11 [95%, CI:-.03/ .24], η2=.04, SMD=.35, NNT=42) was demonstrated.
¹⁰ For three of the 25 primary studies at evidence level 1, the full text is only available in Chinese, so they could not be described in more detail and no risk of bias assessment was performed. Their results are included in the review by Wang et al. (2018) [806].
Risk of Bias Assessment
The Risk of Bias assessment of the 22 RCTs in MT was performed analogously to art therapy and, in summary, found a low Risk of Bias in 15 studies, "some concerns" in four studies, and a high Risk of Bias in three studies. The assessment took place with regard to the five categories of the RoB 2: The high Risk of Bias occurred exclusively in Category 3, "bias due to missing outcome data", due to missing data in the post-test. From a clinical point of view, a high dropout rate (of more than 20% for the classification as high risk) can mostly be explained by the stressful oncological treatment with complex side effects or changed life circumstances. Missing data were handled with adequate methods (intention-to-treat analysis, etc.). Missing or insufficient information in the publications led to the assessment of some concerns for one study in the Category 4, “bias in the measurement of the outcome“, and in three studies in Category 5, “bias in the selection of the reported results“. Except for these cases, the homogeneity of methodological quality was high with a low risk of bias in 15 studies.
Conclusion
The overall findings of music therapy in oncology are positive. There is increasing methodological improvement in conducting clinical trials. Within the creative arts therapies, MT represents the majority of studies on evidence level 1. Across all treatment stages, stable, positive effects on the enhancement of health-related quality of life, the reduction of anxiety and depression, and the reduction of pain can be found for different diagnostic groups and treatment methods. The study findings for fatigue reduction, mood improvement and relaxation, are mixed. Here, further studies are needed to investigate possible positive effects from MT. Other outcomes with hope, satisfaction, positive affect, and spiritual well-being improved with MT; feelings of helplessness and anger could be reduced. With regard to the physiological parameters, the study data is heterogeneous so far. Overall, further studies with high methodological quality are needed in order to determine the process-related influences and mechanisms and contextual factors underlying the improvements.
8.8.3 Dance and Movement Therapy
Dance and movement therapy can be offered to cancer patients to reduce pain, stress and anxiety, and to enhance quality of life.
- Recommendation grade
- 0: offene Empfehlung (Option) bzgl. einer Maßnahme - verwendete Ausdrucksweise = kann
- Level of evidence
- 1b
- Consensus
- Strong consensus (100%)
- References
- [838] [839] [840] [841] [842] [843] [844] [845]
Change note
Artistic therapies (art therapy, dance therapy, music therapy, etc.) can be offered to people with cancer regardless of the level of stress.Dance and movement therapy (DMT) is a practice at the interface of movement, art, and psychotherapy and its interventions are directed towards these three core areas of psychosocial treatment. In contrast to other forms of movement therapy, dance therapy focuses on the creative artistic elements as well as the improvisational elements of movement and the psychotherapeutic aspect. Dance therapy works with active methods such as, the Chace Technique (group process in movement), authentic movement, body image work, stick fighting, and dance and movement elements from different cultures.
Five new reviews ([839], [838], [840], [842], [845]) are available for dance and movement therapy for the period 2012 to 2020. The Cochrane review by Bradt et al. (N=207) [838] includes the primary studies by Dibbell-Hope [846], Sandel et al. [847], and Ho and Fong [848], a conference abstract of the later published study by Ho et al. [843]. The other reviews ([839], [840], [842] are summarized by Koch and Bräuninger in a review [845] which included 13 studies, of which six were RCTs with a total of 282 participants. Of these, two studies are at evidence level 1 ([841], [843], [844]). Other studies have evidence levels 2-4 and are not discussed here.
Meta-analyses and systematic reviews
Results on anxiety reduction are mixed. On the one hand, Boing et al. [839] reported a reduction in fear of recurrence (p=.02). On the other hand, dance and movement therapy interventions did not significantly reduce anxiety (p=.18) in two of the RCTs [846] [848] included in the Cochrane review by Bradt et al. [838].
Mixed results were found in the reviews with regard to depressiveness. On the one hand, in their systematic review, Boing et al. [839] found significant results demonstrating a decrease in depressiveness (p=.01) in one RCT [849]. On the other hand, two RCTs [846], [848] from the review by Bradt et al. [838] found no significant reduction in depressiveness (p=.89).
Regarding the outcome measure stress, only one RCT [844] showed a significant reduction in stress through dance and exercise therapy with a medium effect (d=0.33, p=.039). This study was included in the systematic reviews by Koch and Bräuninger [845], and Boing et al. [839]. Two RCTs [846], [848] from the review by Bradt et al. [838] were unable to demonstrate any significant improvement (p=.24).
For quality of life, Boing et al. [839] summarized the outcomes in regard to mental health (p=.01), environment (p=.029), body image (p<.01), and overall quality of life (p<.01). They also report an improvement in the physical aspects of quality of life (p<.001). The systematic review by Koch and Bräuninger [845] found an increase in quality of life in one RCT [847], while two other RCTs did not demonstrate a significant improvement in quality of life [843] [841]. It should be noted that two RCTs [846][847] from the Cochrane Review by Bradt et al. [838] also found no improvements with regard to body image (p=.58), whereby body image was assessed by different measurement tools in the studies.
With regard to patients' experience of pain, one RCT [843], which was included in the systematic review by Koch and Bräuninger [845] as well as Boing et al. [839], showed a significant reduction in pain intensity (d=.36; p=.035) and pain interference (d=.35; p=.048).
Regarding fatigue, two RCTs [846], [848] in the Cochrane review by Bradt et al. [838] did not show significant improvements (p=.44). The reviews by Boing et al. [839], Goodill et al. [842], and Koch and Bräuninger [845] also report the results of the aforementioned RCTs.
Other positive findings are reported by Boing et al. [839] for social functioning (p=.04), mental health (p=.04), emotional role (p=.07), well-being, and mood (p<.05). Koch and Bräuninger [845] report the results of an RCT [849], which demonstrated a significant improvement regarding life satisfaction (d=2.69; p<.001).
In addition, the influence of dance therapy interventions on various physiological variables was investigated. In the review by Boing et al. [839], one RCT each reported an improvement in functional capacity (p=.03), physical activity (p=.01), strength (p<.05), grip strength and arm volume (p=.028), as well as physical function (p=.001).
Primary studies
The studies described (RCTs) are already included in the reviews by Boing et al. [839] and Koch et al. [845], but are presented again in detail here.
Fear of Recurrence was significantly reduced (p=.02) in the intervention group from Crane-Okada et al. [841], whereas the intervention by Ho et al. [843] showed no effect on participant’s anxiety. Regarding perceived stress, Ho et al. demonstrated a significant reduction in their study (d=0.33; p=.039) [843]. In a secondary analysis of the data on the question of moderator effects of the interventions on stress parameters, Ho et al. [844] found no significant effect of the intervention on cortisol levels over the course of the day after three weeks (B=-0.55; 95% CI: -1.2;0.08).
There was also no significant effect on the quality of life of the intervention groups after a Mindful Movement Program or after six concomitant sessions of DMT [841], [843]. No significant improvements were found on the severity (d=0.01; p=.98) and interference (d=0.14; p=.43) on fatigue, sleep disturbance (d=0.20; p=.24) and depressiveness (d=0.53; p=.11) [843]. Significant improvements were seen in the aforementioned studies in terms of severity (d=0.36; p=.035) and impairment due to pain (d=0.35; p=.048) [843] as well as mindfulness of the IG (post-test: p=.026) in the study by Crane-Okada et al. [841].
Risk of Bias Assessment
The risk of bias assessment of the 2 RCTs for dance and movement therapy was conducted analogously to the process for art and music therapy by three independent raters and showed a consistently low risk of bias (low RoB) across four assessment categories, whereby in Dimension 2, possible bias can be suspected due to the lack of blinding as well as an unequal implementation of the intervention in the study by Crane-Okada et al. [841] (see GL-Report).
Conclusion
The current studies and reviews on dance and movement therapy show an improved, but heterogenous picture with regard to most of the target criteria investigated. Only in a few studies demonstrated a significant reduction of pain and the effects of pain and perceived stress. In addition, in the context of psycho-oncological rehabilitation, there was an increase in life satisfaction, a decrease in the fear of recurrence, and an improvement in mindfulness after dance and movement therapy. The findings on quality of life, depression, fatigue, and upper body mobility were mixed. No effects could be demonstrated for improvement in sleep and body image, although in the latter case, difficulties in the measurability of the construct and a high heterogeneity of the outcome measures should be taken into account.
One should take into account that it is necessary to look not only at the effects but also at the mechanisms of action in order to gain a deeper understanding of the results (for initial findings see: De Witte et al. [850]).
8.8.4 Overlapping Systematic Reviews
From 2012 to 2020, six high-quality, overlapping reviews of the creative arts therapies (CAT) were published, which include 42 studies, 39 of which were RCTs from art, music, and dance therapies (N=3,726) [851], [852], [853], [854], [855], [856].
Converging empirical evidence
Findings on anxiety reduction through creative arts therapies (CAT) are largely positive. Hertrampf et al. [853] reported a significant reduction in anxiety trough CAT in five RCTs (N=478; post-test: 0.12[Tang, Yong et al. 2019] included nine RCTs (N=747) and found a significant reduction in anxiety through CAT in four RCTs (N=337, SMD=-0.48; 95% CI: -0.75;-0.21; p=.0005). A significant reduction in anxiety through CAT was also demonstrated in three RCTs from Archer et al. [851] and in four RCTs from Boehm et al. [852]. Rabadán et al. [854] included 11 studies (N=680) with CAT in patients with breast cancer and found no effect of DMT on anxiety, but a significant reduction in anxiety with MT.
Significant results were also recorded for the reduction of depressiveness. A significant reduction in depressiveness with CAT resulted in five RCTs (N=304) (post-test: 0.14[Hertrampf, Ruth- S. et al. 2017]. Tang et al. [856] (SMD=-6.59; 95% CI: -7.70; -5.47; p<.00001) and Archer et al. [851] also reported positive results in terms of a reduction in depressiveness in two RCTs (N=180) and three RCTs (N=213), respectively. Boehm et al. [852] demonstrated an improvement in depressivity in the IG in five RCTs (N=241), but this was not significant (M: -0.30; 95% CI: -0.60;0.00; p=.05). Only one study in the review by Rabadán et al. [854] failed to show any effects of DMT on depressive symptoms (p=.53) [843].
A reduction in stress was shown not only for CAT in four RCTs (N=262) from the review by Hertrampf et al. [853] (post-test: 0.07[Ho, Rainbow T. H. et al. 2016].
With regard to an increase in quality of life, Hertrampf et al. (post-test: 0.12[Hertrampf, Ruth- S. et al. 2017] and Archer et al. [851] each found improvements in quality of life trough CAT in four RCTs (N=260) and five RCTs, respectively. However, no effect on sleep or quality of life was found by Rabadán et al. [854] after dance and movement therapy. The results from Boehm et al. [852], showed no significant group differences in four RCTs (M=0.15; 95% CI: -0.09;0.40; p=.22) as well.
Positive results are consistently reported for pain reduction. In the review by Hertrampf et al. [853], a moderate to large effect could be observed regarding the reduction of pain on the post-test in four RCTs (N=430) from MM (post-test: 0.54[Rabadán, Jennifer et al. 2017/1/1] showed that dance therapy significantly reduced both the severity (p=.035; d=0.36) and interference of pain (p=.048; d=0.35) [843].
Non-converging evidence
The findings of the studies on the reduction of fatigue show heterogenous results. While Tang et al. [856] found a significant improvement in fatigue in one RCT (N=60; SMD: -1.90; 95% CI: -2.93;-0.87, p=.0003), Ho et al. [843] found no effect of DMT on fatigue (severity: p=0.98; d=0.01; interference: p=.43; d=0.14). Finally, two RCTs (N=170) from CAT on fatigue found no to a moderate effect at post-test (immediately after treatment in Dibbel-Hope [846]; no measurement in Ho et al. [843]), and a small to large effect at follow-up after 3 weeks. Follow-up effects were partly larger than post-test effects (post-test: 0.42[Hertrampf, Ruth- S. et al. 2017]. In another study included in the review by Rabádan et al. [854], fatigue was examined from different aspects. Art therapy significantly reduced fatigue (p=0.007; for patients with mild fatigue), it provided an increase in social well-being (p=.02; for patients with severe general fatigue who had received chemotherapy), it led to an increase in quality of life (p=.034), emotional well-being (p=.017), social well-being (p=.025), and motivation (p=.03; in patients with initially low motivation), and significantly reduced fatigue after six months for patients with severe fatigue [Joly, F. et al. 2016].
The results on the improvement of body image are heterogeneous, which can be largely attributed to the heterogeneity and problematic nature of the outcome measures on body image. The specific review on the outcome body image by Lewis-Smith et al. [855] included three CAT studies up to 2017 (N=110). The authors found no significant improvements in body image trough AT and DMT. The review by Hertrampf et al. [853] included two RCTs (N=79) from CAT on body image improvement, both of which showed no effect or a small effect (0.01[Rabadán, Jennifer et al. 2017] and Archer et al. [851], found improvements in body image.
With regard to strengthening coping strategies (strategies for dealing with illness), no to small effects were reported (0.1[Hertrampf, Ruth- S. et al. 2017]. A review of art therapy also showed no effects on coping strategies [798]. In contrast, the review by Archer et al. [851] found significant improvements in coping strategies in one RCT.
Furthermore, two RCTs (N=79) showed small to medium effects (0.04[Hertrampf, Ruth- S. et al. 2017] of CAT on mental health.
Conclusion
The number and quality of systematic reviews on CAT has increased significantly in recent years. Nevertheless, in many reviews, no meta-analysis could be performed due to the heterogeneity of the primary studies. The heterogeneity can be explained through the use of a wide range of methods, interventions, and measurement instruments. Only Boehm et al. [852] and Tang et al. [856] calculated overlapping effect sizes. Boehm et al. [852] was able to show a significant reduction in anxiety (four RCTs; M= -1.10; 95% CI: -1.4;-0.88; p<.01), whereas Tang et al. [856], in the more recent study, in addition to also demonstrating a significant reduction in anxiety (four RCTs; SMD=-0.48; 95% CI: -0.75;-0.21; p=.0005), was also able to show a significant reduction in depression (two RCTs; SMD=-6.59; 95% CI: -7.70;-5.47; p<.00001) and a significant improvement in fatigue (one RCT) (SMD=-1.90; 95% CI: -2.93;-0.87; p=.0003) through CAT. Thus, the consistently demonstrated reduction in anxiety is the most consistent finding for CAT, with long-term effects also emerging. These findings on the three main outcomes of the overlapping studies are reflected in the individual recommendations and strengthen the evidence base, especially with regard to depression and anxiety reduction.
Evidence tables
Psychotherapeutische Interventionen im Einzel- und Gruppensetting
|
Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Merkmale untersuchter Studien |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Methodische Bemerkungen |
Evidenzklasse |
|
Coutino-Escamilla et al. 2019: "Non-pharmacological therapies for depressive symptoms in breast cancer patients: Systematic review and meta-analysis of randomized clinical trials."2
Eingeschlossene Primärstudien: Marchioro 1996 Savard 2006 Yoo 2009 Garssen 2012 Qiu 2013 Fukui 2000 (2x) Sandgren 2003 (2x) Winzelberg 2003 Delbeault 2009 David 2011 Lee 2013 Ashing 2014 (2x) Heiney 2015 Lewis 2015 Napoles 2015 Kim 2017 Park 2012 Jensen –Johansen 2013 Kim 2009 Cho 2011 Mutrie 2007 Cadmus 2009 (2x) Sprod 2010 Eyigor 2010 Mehnert 2011 Chen 2013 Ratcliff 2016 Bultz 2000 Kalaitzi 2007 Nunes 2007 Hoffman 2012 Chen 2015 Bower 2015 Kenne 2017 (2x) Reich 2017 Culos-Reed 2006 Dannhauer 2009 Kovacs 2012 Cramer 2015 Zhou 2015 Ratcliff 2016 Lanctot 2016
|
MA
Suchzeitraum: Januar 2006 – Dezember 2017
Datenbanken: CENTRAL Medline Embase SCIELO Trip Medical Database PsycNet LILACS EVIPNet
Einschluss-kriterien: P: diagn. Mamma-Ca (nicht terminale Phase) I: nicht-pharmakologische Interventionen C: keine Intervention O: Depressivität S: RCTs
48 RCTS, N=4869 Patientinnen
|
RCTs
Mamma-Ca
Geschlecht: 100% weiblich
Mittleres Alter: kA
Länder : USA (22) Europa (13) Asien (11) Brasilien (1) Türkei (1)
|
Inhalte: 5 x Psychotherapie (CBT, Stress Management) 14x Social Support (Mischkategorie mit Gesprächsgruppen, Telefonbasierten Interventionen, Mailkontakten etc.) 2x Kunsttherapie 2x therap. Lachen 9x Bewegungs-therapie 2x Paartherapie 7x Achtsamkeits-basierte Psychotherapie 7x Yoga
Dauer/Frequenz/ Länge: 20min – 2 Stunden Meist wöchentlich bis zweiwöchentlich 2 – 24 Wochen
Kontrollgruppen: kA |
Primäre Endpunkte: 1. Depressivität
Verwendete Messinstrumente: Depressivität CES-D HADS POMS BDI
|
1. Depressivität àGesamteffekt: Post-Intervention: 48 RCTs, I2 = 96%; SMD=–0.52 [–0.81, –0.22, p < 0.05]
àPsychotherapie: Post-Intervention: 5 RCTs, I2 = 92%; SMD=–0.82 [–1.61, –0.03, p = 0.04] à Sensitivitätsanalyse: nach Entfernung von 2 Ausreißern (Qiu 2013, Savard 2005) weiterhin sign. Reduktion von Depressivität (3 RCTs, I2 =0 %; SMD=–0.77 [–1.06, –0.47, p< 0.05])
|
Keine SUEs berichtet |
Primärstudien: Keine Angaben zu RoB der Primärstudien
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7,9,11,13,15 non-kritischer Dom. 3,6,8,10,12
Sensitivitäts-analysen: Durchgeführt, schrittweise Entfernung einzelner Studien
Starke Heterogenität der Ergebnisse / Entfernung einflussreicher Studien / Subgruppenanalysen (siehe Hauptergebnisse)
Publikations-bias: Visuelle Prüfung Funnel-Plot + Egger's Test / keine Hinweise auf Publication Bias |
1a– |
|
Ye et al. 2018: "A meta-analysis of the efficacy of cognitive behavior therapy on quality of life and psychological health of breast cancer survivors and patients."3
Eingeschlossene Primärstudien: McKiernan 2010 Qiu 2013 Carpenter 2014 Gudenkauf 2015 Groarke 2013 Kissane 2003 Lechner 2014 Duijts 2012 Boesen 2011 Dolbeault 2009 |
MA
Suchzeitraum: August 2017
Datenbanken: CENTRAL Pubmed CINHAL Embase PsyArticles PsycInfo Scopus Web of Science BMJ Clinical Evidence
Einschluss-kriterien: P: diagn. Mamma-Ca I: CBT C: keine Intervention O: QoL, Depressivität, Angst und Distress S: RCTs
10 RCTS, N=1939 Patientinnen
|
RCTs
Mamma-Ca, Stadium 0 - IV
Geschlecht: 100% weiblich
Mittleres Alter: 46 - 54
Länder : USA Irland Frankreich China Australien Niederlande |
Inhalte: CBT
Dauer/Frequenz/ Länge: 60min – 120min wöchentlich 5 - 20 Wochen
Kontrollgruppen: Warteliste TAU Aufmerksamkeits-placebo Pharmakotherapie Entspannungs-training
|
Primäre Endpunkte: 1. QoL 2. Depressivität 3. Angst 4. Distress
Verwendete Messinstrumente: QoL FACT-B
Depressivität CES-D
Angst SAS
Distress PSS |
1. QoL àGesamteffekt: Post-Intervention: 9 RCTs, I2 = 36%; SMD=0.57 [0.44, 0.69, p < .001]
2. Depressivität àGesamteffekt: Post-Intervention: 6 RCTs, I2 = 47%; SMD=–1.11 [–1.28, –0.94, p<.001>
3. Angst àGesamteffekt: Post-Intervention: 5 RCTs, I2 = 36%; SMD=–1.10 [–1.27, –0.03, p<.001>
4. Distress àGesamteffekt: Post-Intervention: 5 RCTs, I2 = 6%; SMD=–0.40 [–0.53, –0.26, p<.001> |
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 4 PB: 6 DB: 5 AB: 7 RB: 9 OB: 7
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7 non-kritischer Dom. 3
Sensitivitäts-analysen: Mäßige Heterogenität/ bei Depressivität ließ sich Heterogenität durch Herkunftsland aufklären (USA vs. Not USA)
Publikations-bias: Visuelle Prüfung Funnel-Plot + Egger's Test / keine Hinweise auf Publication Bias
|
1a |
|
Sanjida et al. 2018: "Are psychological interventions effective on anxiety in cancer patients? A systematic review and meta-analyses."4
Eingeschlossene Primärstudien: 71 Primärstudien in qual. Review / 51 in Meta-Analysen
|
SysRev & MA
Suchzeitraum: Januar 1993– Juni 2017
Datenbanken: CENTRAL Medline Embase CINHAL Scopus PsycInfo
Einschluss-kriterien: P: erwachsene Krebspatienten I: psychosoziale Intervention C: alternative Intervention, TAU/UC, Warteliste O: Angst, Distress S: RCTs
71 RCTS, N=13098 Patientinnen
51 RCTs, N=8283 Patientinnen in MA
|
RCTs
Brustkrebs (36) Gynäkologische Tumore (3) Prostata- und Hodenkrebs (2) Sonstige Krebsidiagnosen (29)
Geschlecht: 74,6% weiblich
Mittleres Alter: 55
Länder : USA (19) Europa (29) Weitere (53)
|
Inhalte: 14 x CBT 12 x Entspannungs-verfahren 9x Psychosoziale Therapie 13x "Supportive Care Interventions" 3x gestufte Interventionen ("stepped care") 20x sonstige
Dauer/Frequenz/ Länge: 4 Tage – ein Jahr
Kontrollgruppen: alternative Intervention TAU/UC Warteliste |
Primäre Endpunkte: 1. Angst
Verwendete Messinstrumente: Angst HADS STAI POMS
|
1. Angst àGesamteffekt: Post-Intervention: 51 RCTs, n=7491 I2 = 68%; SMD=–0.21 [–0.30, –0.13, p < .001] à Sensitivitätsanalyse: Entfernung der Studie mit größtem und kleinsten Effekt, keine Änderung des Ergebnis
àCBT: Post-Intervention: 9 RCTs, I2 = 14%; SMD=–0.08 [–0.20, 0.05, p >.05]
àSupportiv expressive Therapie: Post-Intervention: 4 RCTs, I2 = 68%; SMD=–0.16 [–0.35, 0.03, p>.05]
àPsychotherapie: Post-Intervention: 4 RCTs, I2 = 0%; SMD=0.07 [–0.09, 0.23, p>.05]
|
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 18 PB: 2 DB: 7 AB: 42 RB: 48 OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 7,11,15, non-kritischer Dom. 5,8
Sensitivitäts-analysen: durchgeführt, siehe Hauptergebnisse
Durchführung von Subgruppen-analysen, teilweise in Hauptergebnissen aufgeführt
Publikations-bias: "Studies with a sample size of less than 40 participants were excluded to reduce the potential influence of publication bias and inflated ES common in small studies. (p.2065)"
|
1a |
|
Kalter et al. 2018: "Effects and moderators of psychosocial interventions on quality of life, and emotional and social function in patients with cancer: An individual patient data meta-analysis of 22 RCTs." 5
Eingeschlossene Primärstudien: 61 RCTs, davon 22 in IPD-Meta-Analyse Armes 2007 Arving 2007 Braamse 2015 Chambers 2013 Duijts 2012 Ell 2008 Ferguson 2012 Gellaitry 2010 Gielissen 2006 Goedendorp 2010 Graves 2003 Heiney 2003 Johansson 2008 Kimman 2011 Mann 2012 Meneses 2007 Northouse 2005 Nothouse 2007 Northouse 2013 Savard 2005 Savard 2006 Van der Berg 2015
|
IPD MA
Suchzeitraum: Oktober 2017
Datenbanken: Medline Embase CINHAL PsycInfo
Einschluss-kriterien: P: erwachsene Krebspatienten I: Informations-vermittlung, Support, CST, Psychotherapie C: TAU/UC, Warteliste, Aufmerksamkeits-placebo O: QoL + weitere Outcomes S: RCTs
22 RCTs, N=4217 Patientinnen in IPD-MA
|
RCTs
Brustkrebs (13) Hämatologischer Krebs (1) Prostatakrebs (2) Gemischte Krebsidiagnosen (6)
Geschlecht: 65% weiblich
Mittleres Alter: 56 (SD=11.4)
Länder : USA (8) Niederlande (6) Kanada (2) Schweden (2) Australien (1) UK (3)
|
Inhalte: CST (19) Psychotherapie (2) Informations-vermittlung (1) Support (-)
Dauer/Frequenz/ Länge: 4-52 Wochen 1-54 Sitzungen (teils Langzeit-einzeltherapie) Individual-, Gruppen-, und Paarsetting
Kontrollgruppen: TAU/UC (14) Warteliste (6) Aufmerksamkeits-placebo (2) |
Primäre Endpunkte: 1. QoL
Sekundäre Endpunkte: 1. Emotionales Funktions-niveau 2. Soziales Funktions-niveau
Verwendete Messinstrumente: QoL FACT-G EORTC QLQ-C30 SF-36 QoL-CS
|
1. QoL àGesamteffekt: Post-Intervention: 22 RCTs, n=4217 SMD=0.14 [0.06, 0.21, p<.05>
Interventionstyp als sign. Moderator (p=.01): àInformations-vermittlung: Post-Intervention: 1 RCTs, SMD=0.19 [0.03, 0.34, p <.05> àCST: Post-Intervention: 19 RCTs, SMD=0.09 [0.04, 0.15, p <.05> àPsychotherapie: Post-Intervention: 2 RCTs, SMD=0.32 [0.12, 0.51, p <.05>
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Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 15 PB: nicht erfasst DB: nicht erfasst AB: 17 RB: 18 OB: kA "Items related to blinding were omitted because blinding of patients and personnel is difficult in case of a PSI. Also, the rating of blinding of outcome assessors was excluded because QoL, EF, and SF were assessed using patient‐reported outcomes (PROs)." (p.1153)
Review: AMSTAR-2: low quality Method.Mängel in kritischer Domäne 7 non-kritischer Dom. 3,12,14
Sensitivitäts-analysen: Durchführung von Moderatoren-analysen, teilweise in Hauptergebnissen aufgeführt
Publikations-bias: Visuelle Prüfung Funnel-Plot + Egger's Test / keine Hinweise auf Publication Bias
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1a |
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Hilfiker et al. 2018: "Exercise and other non-pharmaceutical interventions for cancer-related fatigue in patients during or after cancer treatment: a systematic review incorporating an indirect-comparisons meta-analysis."6
Eingeschlossene Primärstudien: 245 Primärstudien |
Indirect-comparison MA
Suchzeitraum: Januar 2017
Datenbanken: Pubmed CENTRAL
Einschluss-kriterien: P: erwachsene Krebspatienten I: Bewegungs- oder nicht-pharmakologische Therapie C: TAU/UC O: Fatigue S: RCTs
112 RCTs in MA Intervention während laufender Krebsbehandlung
133 RCTs in MA Interventionen nach abgeschlossener Krebsbehandlung
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RCTs
Brustkrebs (126) Hämatologischer Krebs (10) Prostatakrebs (18) Kolorektaler Krebs (7) Gemischte Krebsidiagnosen (52)
Geschlecht: >65% weiblich
Mittleres Alter: kA
Länder : Keine zusammenfas-senden Angaben, Details in Appendices
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Inhalte: Während Behandlung Ausdauer (34) Ausdauer + Gewichte (23) CBT (18) Entspannung (12) à inkl. Atmung, Stretching, Meditation Yoga (10) Gewichte (10) Multimodal (6) Massage (4) Heilende Berührung (3) Tanztherapie (2) Musiktherapie (1)
Nach Behandlung Ausdauer (30) Ausdauer + Gewichte (32) CBT (29) Entspannung (kA) à inkl. Atmung, Stretching, Meditation Yoga (kA) Gewichte (kA) Multimodal (kA) Massage (kA) Heilende Berührung (kA) Tanztherapie (kA) Musiktherapie (kA)
Dauer/Frequenz/ Länge: 3-52 Wochen 0-12 Wochen Follow-Up Individual-, Gruppen-, und Paarsetting, Tele- und EHealth
Kontrollgruppen: TAU/UC |
Primäre Endpunkte: 1.Fatigue
Verwendete Messinstrumente: CFS PFS EORTC QLQ-C30 Fatigue BFI POMS FACIT-F FACT-F etc.
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1. Fatigue Während Behandlung àCBT: Post-Intervention: 18 RCTs, I2 = 61%; SMD=–0.20 [–0.57, 0.17, p >.05] àEntspannung: Post-Intervention: 12 RCTs, I2 = 88%; SMD=–0.77 [–1.22, –0.31, p <.05>
Nach Behandlung àCBT: Post-Intervention: 29 RCTs, I2 = 76%; SMD=–0.42 [–0.58, –0.25, p <.05> àEntspannung: Post-Intervention: ? RCTs, I2 = ? %; SMD=–0.05 [–0.64, 0.53, p <.05>
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Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB "Over all comparisons, the random sequence generation was adequate in most trials (97%); allocation concealment was problematic in 61% of the trials. Baseline characteristics were not balanced in 17% of the studies; patients and outcome assessor could not be blinded in most trials (99%), therapists were never blinded. More than 15% of drop-outs were present in 36% of the trials and only 51% of the trials reported an intention-to-treat analysis. (p.654)
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,11,15 non-kritischer Dom. 1,3,10
Sensitivitäts-analysen: Ausschluss von Studien mit n<25 Teilnehmern pro Arm; Effekte generell kleiner, keine Änderung des Signifikanzniveaus in relev. Effekten; kein Einfluss auf Heterogenität
Publikations-bias: Egger's Test liefert Hinweise Publikations-Bias in relev. Vergleichen
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1a- |
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Hall et al. 2018: "Mind-body interventions for fear of cancer recurrence: A systematic review and meta-analysis."7
Eingeschlossene Primärstudien: Bailey 2004 Bannaasan 2015 Crane-Okada 2012 Chow 2014 Dieng 2016 Dodds 2015 Heinrichs 2012 Herschbach 2010 Lenagacher 2009, 2016 Mishel 2002 Van der Wal 2017 Ye 2016 |
MA
Suchzeitraum: Mai 2017
Datenbanken: Medline PsychInfo Embase CINHAL Web of Science CENTRAL
Einschluss-kriterien: P: erwachsene Krebspatienten I: Mind-Body Ansatz (auch CBT, Entspannung etc.) C: aktive Kontrolle, TAU/UC O: Rezidivangst S: RCTs
19 RCTS, N=2806 Patientinnen (18 RCTs in MA)
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RCTs
Brustkrebs (11) Prostatakrebs (3) Gynäkologischer Krebs (1) Melanom (1) Gemischte Krebsidiagnosen (3)
Geschlecht: >65% weiblich
Mittleres Alter: kA
Länder : Belgien (19 China (2) Deutschland (2) Niederlande (1) Thailand (1) USA (12)
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Inhalte: CBS (11) Entspannung (4) à keine separate Auswertung Achtsamkeit (10)
Dauer/Frequenz/ Länge: 9 Tage-12 Monate (Modalw.=1Monat) 4-17 Sitzungen (median=6) 10–165min Sitzungsdauer (median=120)
Individual-, Gruppen-, und Paarsetting, Tele- und EHealth
Kontrollgruppen: Aktive Kontrolle (9) TAU/UC (10) |
Primäre Endpunkte: 1. Rezidivangst
Verwendete Messinstrumente: MUIS CARS CCSQ FCRS FCRI FoP GTUS MCCS IUS‐SF MAX‐PC‐FCR |
1. Rezidivangst àGesamteffekt: Post-Intervention: 18 RCTs, I2 = 48%; SMD=–0.36 [–0.49, –0.23, p <.001> Fail-Safe-N: 247
Longest Follow-Up: 14 RCTs, I2 = 63%; SMD=–0.31 [–0.47, –0.16, p <.001>
àCBS: Ausreißer (Bannaasan 2015) ausgeschlossen Post-Intervention: 12 RCTs, I2 = ? %; SMD=–0.26 [–0.39, –0.13, p <.001>
Longest Follow-Up: ? RCTs, I2 = ? %; SMD=–0.19 [–0.80, –0.01, p =.049]
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Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 4 PB: 8 DB: 4 AB: 11 RB: 14 OB: 5 (Baseline imbalance und Differential attrition)
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7 non-kritischer Dom. 1
Sensitivitäts-analysen: Durchgeführt, schrittweise Entfernung einzelner Studien; siehe Hauptergebnisse
Subgruppen-analysen (siehe Hauptergebnisse)
Publikations-bias: Funnel-Plot; keine Hinweise
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1a |
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Cobeanu et al. 2018: "Alleviation of Side Effects and Distress in Breast Cancer Patients by Cognitive-Behavioral Interventions: A Systematic Review and Meta-analysis."8
Eingeschlossene Primärstudien: Antoni 2001, 2002, 2006a,b, Arving 2007 Berger 2009a,b Brifge 1988 Cohen 2007 Crues 2000 Gaston-Johansson 2000 Given 2008 Groarke 2012 Kissane 2003 Marchioro 1996 Molassiotis 2002 Montgomery 2009 Nunes 2007 Schnur 2009 Walker 1999 Yoo 2005 |
MA
Suchzeitraum: Bis Dezember 2015
Datenbanken: Medline PsychInfo
Einschluss-kriterien: P: erwachsene Krebspatienten I: Kognitive und/oder behaviourale Interventionen während adjuvanter Theapie C: Standard-versorgung O: SUEs, Distress (auch Angst, Depressivität) S: RCTs
19 RCTS, N=2037 Patientinnen
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RCTs
Brustkrebs, Stadien I - IV
Geschlecht: 100% weiblich
Mittleres Alter: 42 - 55
Länder : kA
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Inhalte: CBT (14) Verhaltenstherapie (5)
Dauer/Frequenz/ Länge: 3 – 33 Stunden
Individual- und Gruppensetting, teilweise Entspannungs-verfahren (PMR, Imagination) sowie Tele- und EHealth mit eingesetzt
Kontrollgruppen: TAU/UC (18) Automatisierte edukative Intervention (1) |
Primäre Endpunkte: 1. Distress (schließt Depressivität, Angst mit ein!) 2. Depressivität 3. Angst 4. QoL 5. Übelkeit/Er-bechen 6. Fatigue 7. Schlafstörungen 8. Schmerz
Verwendete Messinstrumente: Distress MHI-5 CARES ABS PSOM POMS BSI PSS MR RSCL MRS
Depressivität HADS BDI
Angst HARS HADS STAI Einzelitems
QoL CARES BFS SIP LCS EORTC QLQ-C30 MOS-SF-36-v2 FAD FACT-B
Übelkeit/Erbrechen MANE
Fatigue FSI
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1. Distress àGesamteffekt: Post-Intervention: 16 RCTs, N=1831 I2 = 65%; SMD=-0.30 [0.13, 0.48, p <.001> Fail-Safe-N: 126 Ausschluss von zwei Ausreißern (Given 2008, Schnur 2009) 14 RCTs, I2 = 51%; SMD=-0.29 [0.15, 0.44, p <.001>
Follow-Up: 7 RCTs, I2 = 47%; SMD=-0.21 [0.05, 0.37, p =.008]
2. Depressivität àGesamteffekt: Post-Intervention: 10 RCTs, N=1202 I2 = 70%; SMD=-0.21 [–0.01, 0.45, p =.063] Fail-Safe-N: 126
Follow-Up: 4 RCTs, I2 = 0%; SMD=-0.10 [–0.04, 0.24, p =.165]
3. Angst àGesamteffekt: Post-Intervention: 8 RCTs, N=1083 I2 = 73%; SMD=-0.28 [0.02, 0.54, p =.033] Fail-Safe-N: 29
Follow-Up: 4 RCTs, I2 = 22%; SMD=-0.11 [–0.05, 0.27, p =.170]
4. QoL àGesamteffekt: Post-Intervention: 8 RCTs, N=1139 I2 = 72%; SMD=0.45 [0.21, 0.69, p <.001> Fail-Safe-N: 86 Ausschluss von einem Ausreißer (Marchioro 1996) 7 RCTs, I2 = 45%; SMD=0.33 [0.16, 0.50, p <.001>
Follow-Up: 7 RCTs, N=1159 I2 = 94%; SMD=0.46 [–0.01, 0.95, p =.056] Ausschluss von einem Ausreißer (Antoni 2006) 6 RCTs, I2 = 5%; SMD=0.15 [0.02, 0.28, p =.022]
5. Übelkeit/Erbr. àGesamteffekt: Post-Intervention: 5 RCTs, N=518 I2 = 0%; SMD=-0.39 [0.22, 0.58, p <.001>
6. Fatigue àGesamteffekt: Post-Intervention: 6 RCTs, N=831 I2 = 84%; SMD=-0.34 [–0.02, 0.71, p =.063]
Follow-Up: 2 RCTs, N=324 I2 = 83%; SMD=-0.35 [–0.20, 0.90, p =.209]
7. Schmerz àGesamteffekt: Post-Intervention: 3 RCTs, N=397 I2 = 18%; SMD=0.02 [–0.26, 0.21, p =.854]
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Keine SUEs berichtet |
Primärstudien: Keine RoB-Bewertung durchgeführt!
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7,9,13 non-kritischer Dom. 3,5,8,10,12
Sensitivitäts-analysen: Modertoren-analyse für Haupteffekte bei hoher Heterogenität
Publikations-bias: Fail-Safe-N berechnet (siehe Hauptergebnisse); Funnel-Plot; Trim-and-Fill-Procedure |
1a- |
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Bauereiß et al. 2018: "Effects of existential interventions on spiritual, psychological, and physical well-being in adult patients with cancer: Systematic review and meta-analysis of randomized controlled trials."9
Eingeschlossene Primärstudien: Ando 2010 Breitbart 2010, 2012, 2015 Carlson 2016, 2013 Chochinov 2011 Classen 2001 Butler 2009 Giese-Davis 2002 Classen 2008 Dubbleby 2007 Gagnon 2015 Goodwin 2001 Bordeleau 2003 Hall 2011 Henry 2010 Herth 2000 Ho 2016 Juliao 2013, 2014 Kissane 2003, 2007 Lee 2006 Lloyd-Williams 2013, 2018 Lo 2016 Mok 2012 Rutsoen 1998 Spiegel 1981 Tabrizi 2016 Van der Spek 2017 Vuksanovic 2017 Xiao 2013 Ye 2017
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MA
Suchzeitraum: Januar 2018
Datenbanken: Medline PsychInfo Psyndex Embase CINAHL CENTRAL ICTRP
Einschluss-kriterien: P: erwachsene Krebspatienten I: "existential interventions" C: aktive & inaktive Kontrolle O: Primär: Spirituelles Wohlbefinden, Angst, Depressivität S: RCTs
30 RCTS, N=3461 Patientinnen (24 RCTs in MA)
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RCTs
Fortgeschrittene krebserkrankung (22) Frühstadium (4) Rezidivierende Krebserkrankung (1) Krebs-Überlebende (3) Gemischte Stichprobe mit anderen terminalen Erkrankungen (krebs >90%) (2)
Geschlecht: kA
Mittleres Alter: 57
Länder : USA (7) Japan (1) Kanada (9) Australien (4) UK (3) China (4) Portugal (1) Norwegen (1) Iran (1) Niederlande (1)
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Inhalte: Sinnbasierte Interventionen (9) Supportiv-expressive Gruppenth. (9) Kognitiv-existentielle Therapie (2) "Life Review" (4) "dignity therapy" (4)
davon Einzel (14) Gruppe (15) Beides (1)
Dauer/Frequenz/ Länge: 1 – 52 Wochen bei wöchentlicher Frequenz
Kontrollgruppen: Warteliste oder TAU/UC (18) Massage, Entspannung, Stress management (3) Supportive therapie (5) Psychoedeukation (3) "Mindfulness-based cancer recovery" (1) |
Primäre Endpunkte: 1. Spirituelles Wohlbefinden 2. Depressivität 3. Angst
Sekundäre Endpunkte: 1. Existentielles Wohlbefinden 2. QoL 3. Hoffnung 4. DHD 5. Selbstwirksam-keitserleben 6. Physisches Wohlbefinden 7. Schmerz
Verwendete Messinstrumente: Depressivität HADS BDI POMS CHADS ESAS
Angst HADS POMS CHADS ESAS
QoL MQoL FACT-B FACIT-Sp EORTC QLQ-C30 EQ-5D QoLC-E FACT-G
Schmerz EORTC QLQ-C30 PRS Einzelitems |
1. Depressivität Post-Intervention: 14 RCTs, I2 = 58%; SMD=-0.15 [–0.01, 0.32, p >.05] Nach Ausschluss von Studien mit sign. Baseline-Unterschieden (Carlson 2013, 2016, Breitbart 2015, Lloyd-Williams 2013, 2018): 11 RCTs, I2 = 32%; SMD=-0.25 [0.10, 0.39, p <.05>
Follow-Up 1 7 RCTs, I2 = 5%; SMD=0.06 [–0.24, 0.12, p >.05]
Follow-Up 2 3 RCTs, I2 = 55%; SMD=0.02 [–0.32, 0.28, p >.05]
Follow-Up 3 3 RCTs, I2 = 21%; SMD=0.04 [–0.23, 0.15, p >.05]
2. Angst Post-Intervention: 13 RCTs, I2 = 71%; SMD=-0.12 [–0.08, 0.32, p >.05] Nach Ausschluss von Studien mit sign. Baseline-Unterschieden (Carlson 2013, 2016, Breitbart 2015, Lloyd-Williams 2013, 2018): 11 RCTs, I2 = 64%; SMD=-0.21 [0.00, 0.41, p =.05]
Follow-Up 1 7 RCTs, I2 = 29%; SMD=0.05 [–0.26, 0.16, p >.05]
Follow-Up 2 3 RCTs, I2 = 74%; SMD=0.00 [–0.39, 0.39, p >.05]
Follow-Up 3 3 RCTs, I2 = 71%; SMD=0.03 [–0.35, 0.30, p >.05]
3. QoL Post-Intervention: 17 RCTs, I2 = 75%; SMD=0.21 [0.01, 0.42, p <.05> Nach Ausschluss von Studien mit sign. Baseline-Unterschieden (Carlson 2013, 2016, Breitbart 2015, Lloyd-Williams 2013, 2018): 16 RCTs, I2 = 74%; SMD=0.21 [0.02, 0.48, p <.05>
Follow-Up 1 8 RCTs, I2 = 45%; SMD=0.18 [–0.06, 0.42, p >.05]
Follow-Up 2 4 RCTs, I2 = 66%; SMD=0.12 [–0.21, 0.45, p >.05]
Follow-Up 3 2 RCTs, I2 = 90%; SMD=0.16 [–0.67, 0.99, p >.05]
4. Schmerz Post-Intervention: 5 RCTs, I2 = 74%; SMD=-0.21 [–0.07, 0.49, p >.05]
Follow-Up 1 1 RCTs, I2 = – %; SMD=-0.29 [–0.15, 0.72, p >.05]
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Keine der Primärstudien hat systemtisch SUEs erfasst. |
Primärstudien: RCTs mit low RoB SB: 11 PB: nicht erfasst DB: nicht erfasst AB: 16 RB: 14 OB: 18
"Because blinding of participants and personnel is in general not feasible in psychological interventions and outcome assessors were participants themselves, evaluations on these two domains are not provided." (p. 2533)
Review: AMSTAR-2: low quality Method.Mängel in kritischer Domäne 7 non-kritischer Dom. 6,10
Sensitivitäts-analysen: Ausschluss von Studien mit sign. Baselineunter-schieden auf Outcomemaßen (siehe Hauptergebnisse); Ausschluss aller Studien mit hohem Bias-Risiko à keine Ergebnis-veränderung
Publikations-bias: Für MA mit k>10 Studien bestimmt. Asymmetrische Funnel-Plots jedoch keine sign. Egger's Tests bei relevanten Outcomes |
1a |
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Zhang et al. 2017: "Effects of cognitive behavioral therapy on quality of life and stress for breast cancer survivors: a meta-analysis."10
Eingeschlossene Primärstudien: Groarke 2013 Mishel 2005 Savard 2005 Cruess 2000 Edmonds 1999 Marchioro 1996 |
MA
Suchzeitraum: Februar 2014
Datenbanken: Medline Embase CENTRAL Google Scholar
Einschluss-kriterien: P: Brustkrebs-patientinnen I: CBT C: - O: QoL, Distress S: RCTs
6 RCTs, N=430 Patientinnen
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RCTs
Brustkrebs, Stadien I-IV
Geschlecht: 100% weiblich
Mittleres Alter: 45 - 64
Länder : kA
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Inhalte: CBT (1) Kognitiv-behaviourales Stressmanagement (4) Sonst. Psychologische Intervention (1)
davon face-to-face (5) Telefon (1)
Dauer/Frequenz/ Länge: 4 – 35 Wochen Wöchentliche Frequenz Sitzungsdauer 50 – 180min
Kontrollgruppen: Tau/UC (1) Wartelist (2) Nicht-psychologische Intervention (1) kA (2) |
Primäre Endpunkte: 1. QoL
Sekundäre Endpunkte: 2. Distress
Verwendete Messinstrumente: QoL EORTC QLQ-C30 FLIC
Distress PSS POMS HADS BDI |
1. QoL Post-Intervention: 3 RCTs, I2 = 86%; SMD=–0.016 [–0.90, 0.87, p =.972] Random-effects model à Sensitivitätsanalyse: nach Ausschluss von Marchioro 1996 sign. Größerer Effekt in IG: Post-Intervention: 2 RCTs, I2 = ? %; SMD=0.46 [0.09, 0.83, p =.014]
2. Distress Post-Intervention: 4 RCTs, I2 = 0%; SMD=–0.125 [–0.27, 0.02, p =.084] Fixed-effects model |
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 6 PB: 0 DB: 1 AB: 2 RB: 6 OB: -
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,9,13,15 non-kritischer Dom. 1,3,8,10,12,16
Sensitivitäts-analysen: Schrittweiser Ausschluss einzelner Studien; nur Ausschluss von Marchioro 1996 hat sign Einfluss (siehe Hauptergebnisse)
Publikations-bias: Nicht geprüft, da k<5 Studien pro Outcome
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1a- |
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Xiao et al. 2017: "Effectiveness of Psychological Interventions on Depression in Patients After Breast Cancer Surgery: A Meta-analysis of Randomized Controlled Trials."11
Eingeschlossene Primärstudien: Chan 2015 Cousson-Gélie 2011 Deng 2013 Du 2011 Ellyn 2014 Huang 2013 Jiang 2013 Hou 2015 Marchioro 1996 Yang 2014 Zhang 2012 Zhao Hui 2011 Zhao Jun 2009 |
MA
Suchzeitraum: kA
Datenbanken: Medline Pubmed CENTRAL WANGFANG CKNI VIP
Einschluss-kriterien: P: Brustkrebs-patientinnen nach OP I: Einzel-CBT C: keine Intervention O: Primär : Depressivität S: RCTs/CCTs
13 RCTs, N=966 Patientinnen
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RCTs/CCTs
Brustkrebs-patientinnen nach operativem Eingriff, keine klinisch relevante Depression
Geschlecht: 100% weiblich
Alter: 24 - 76
Länder : China (10) Frankreich (1) USA (1) Italien (1)
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Inhalte: CBT (9) à beinhaltet in 8/9 Fällen auch Entspannungs-training und Psychoedukation Psychologische Beratung (4)
Dauer/Frequenz/ Länge: 2 Wochen – 9 Monate
Kontrollgruppen: kA |
Primäre Endpunkte: 1. Depressivität
Verwendete Messinstrumente: Depressivität SDS HADS HAMD |
1. Depressivität Post-Intervention, SDS: 8 RCTs, N=688 I2 = 0%; SMD=–0.87 [–1.03, –0.71, p <.001>
Post-Intervention, HADS: 3 RCTs, N=132 I2 = 44%; SMD=-0.50 [–0.98, –0.02, p =.04]
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Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: kA PB: kA DB: kA AB: kA RB: kA OB: kA
Nutzt Jadad-Score: Range=3-4
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7 non-kritischer Dom. 8,10,16
Sensitivitäts-analysen: Ausschluss von „low quality“ Studien ändert nichts an Ergebnissen, keine Details dazu
Publikations-bias: Asymmetrische Funnel-Plots liefern Hinweise auf Pub.-Bias. Geringe anzahl an eingeschl. Studien.
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1a |
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Hsieh et al. 2017: "The effects of supportive care interventions on depressive symptoms among patients with lung cancer: A metaanalysis of randomized controlled studies."12
Eingeschlossene Primärstudien: Bredin 1999 Wu 2003 Chen 2006 Ni 2009 Carlson 2010 Porter 2011 Yao 2012 Walker 2014 Badr 2015 Morano 2014 Chen 2015 Molassiotis 2015a, b
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MA
Suchzeitraum: September 2015
Datenbanken: Embase Pubmed CENTRAL CEPS
Einschluss-kriterien: P: Lungenkrebs I: "supportive care": nicht-pharmakologisch, nicht invasiv, Förderung und Erhaltung von Wohlbefinden und Krankheitsverarbeitung C: TAU/UC O: Depressivität S: RCTs
12 RCTs, N=1472 Patientinnen
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RCTs
Lungenkrebs, Stadien I-IV, teils komorbide COPD, eine Studie mit komorbider Depression als Einschluss-kriterium
Geschlecht: kA
Alter: 56 - 71
Länder : China (4) UK (3) USA (2) Kanada (1) Brasilien (1) Taiwan (1)
|
Inhalte: CBT + Psychoedukation (5) Psychoedukation (4) Sport- und Bewegungstherapie (3)
davon Face-to-face (8) Telefon (4)
Dauer/Frequenz/ Länge: 6 – 60 Sitzungen 4 -32 Wochen
Kontrollgruppen: Tau/UC (10) Edukation (2) |
Primäre Endpunkte: 1. Depressivität
Verwendete Messinstrumente: Depressivität SDS PSSCAN BDI SCL HADS PROMIS |
1. Depressivität àGesamteffekt: Post-Intervention: 12 RCTs, N=1472 I2 = 88%; SMD=–0.75 [–1.07, –0.41, p <.001>
àCBT: Post-Intervention: 5 RCTs, N=515 I2 = 14%; SMD=–1.05 [–1.25, –0.85, p <.001>
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Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 7 PB: ka DB: 8 AB: 8 RB: kA OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7,15 non-kritischer Dom. 3,5,10
Sensitivitäts-analysen: Schrittweiser Ausschluss kleiner (N<50) Studien und Studien mit High-RoB führten zu keiner Änderung der Ergebnisse
Publikations-bias: "Finally, the existence of a publication bias cannot be ignored. It should be noted that publication bias has some effect on the available evidence pool." (p. 721)
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1a- |
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Jassim et al. 2015: "Psychological interventions for women with non‐metastatic breast cancer."13
Eingeschlossene Primärstudien: Andersen 2004, 2007, 2008 Antoni 2001, 2006a, b, 2009 Badger 2007 Baucom 2009 Boesen 2011 Classen 2008 Cohen 2007 Dolebeault 2009 Ferguson 2012 Fillion 2008 Fukui 2000 Garssen 2012 Graves 2001, 2003 Henderson 2012 Kissane 2003, 2004 Loprinzi 2011 Manne 2007 Marchioro 1996 Marcsu 2010 Mishel 2005, 2006 Narváez 2008 Nunes 2007 Richardson 1997 Simpson 2001 Taylor 2003 Vos 2004, 2006 Yates 2005
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MA
Suchzeitraum: May 2013
Datenbanken: CBCG Specialized Register CENTRAL Medline Embase PsycINFO CINAHL ICTRP ClinicalTrials.gov CancerLit PsyLit Iranmedex Indmed
Einschluss-kriterien: P: Brustkrebspatient-innen, Stadien I-III I: CBT, Psychotherapie, Counselling, Psychoedukation C: Placebo, TAU/UC, Warteliste, alternative pysych. Intervention O: Primär: Depressivität, Angst, Distress, "mood disturbance" S: RCTs
28 RCTS, N=3940 Patientinnen (16 RCTs in MA)
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RCTs
Mamma-Ca, "Frühstadium", keine Metastasen
Geschlecht: 100% weiblich
Alter: Zw. 18 - 80
Länder : USA (15) Europa (6) Kanada (2) Japan (1) Australien (2) Israel (1) Brasilien (1)
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Inhalte: CBT-basiert (24) Sonst. Psychotherapie-ansätze (4)
davon Einzel (8) Gruppe (20)
Face-to-Face, teils + Telefon (25) Ausschl. telefonbasiert (3)
Dauer/Frequenz/ Länge: 1 – 39 Stunden, M=14, SD=9.65 bei wöchentlicher Frequenz
Kontrollgruppen: Keine genaueren Angaben, siehe Spalte "Studientyp" |
Primäre Endpunkte: 1. Depressivität 2. Angst 3. Distress 4. Stimmungs-störungen
Sekundäre Endpunkte: 5. QoL 6. Coping 7. Anpassung 8. Überlebensrate
Verwendete Messinstrumente: Depressivität HADS BDI CES-D
Angst HADS STAI BAI HAMA
Distress IES BSI MHI
QoL QLQ-BR23 FACT-B LASA EORTC QLQ-C30 QoL-CS FLIC QLI CARES-SF
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1. Depressivität à Gesamteffekt Post-Intervention: 7 RCTs, N=637 I2 = 95%; SMD=–1.01 [–1.83, –0.18, p =.02] Nach Ausschluss von Ausreißer (Garssen 2013): 6 RCTs, N=567 I2 = 82%; SMD=–0.43 [–0.90, 0.04, p =.07] GRADE: low quality à Gruppe (<20h) Post-Intervention: 3 RCTs, N=120 I2 = 39%; SMD=–0.33 [–0.80, 0.14, p =.17] à Gruppe (>20h) Post-Intervention: 1 RCTs, N=303 I2 = na; SMD=–0.10 [–0.32, 0.13, p =.41] à Einzel (<20h) Post-Intervention: 2 RCTs, N=144 I2 = 96%; SMD=–1.00 [–3.19, 1.20, p =.37]
2. Angst à Gesamteffekt Post-Intervention: 8 RCTs, N=776 I2 = 95%; SMD=–0.48 [–0.76, –0.21, p <.01> GRADE: low quality à Gruppe (<20h) Post-Intervention: 5 RCTs, N=358 I2 = 68%; SMD=–0.44 [–0.85, –0.03, p =.04] à Gruppe (>20h) Post-Intervention: 2 RCTs, N=323 I2 = 64%; SMD=–0.53 [–1.32, 0.26, p =.19] à Einzel (<20h) Post-Intervention: 1 RCTs, N=95 I2 = na; SMD=–0.78 [–1.20, –0.36, p <.01>
3. Distress keine MA aufgrund fehlender Varianzangaben
2/2 Studien zeigen sign. reduzierten Distress zugunsten der IG
4. QoL à Gruppe Post-Intervention: 5 RCTs, N=578 I2 = 47%; SMD=0.21 [–0.03, 0.46, p =.08] GRADE: low quality à Einzel Post-Intervention: 3 RCTs, N=141 I2 = 41%; SMD=0.65 [0.07, 1.23, p =.03] GRADE: very low quality Test für Subgruppenunter-schiede nicht signifikant
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Keine der Primärstudien hat SUEs berichtet. |
Primärstudien: RCTs mit low RoB SB: 4 PB: 0 DB: 5 AB: 7 RB: 24 OB: 19
Review: AMSTAR-2: high quality Method.Mängel in kritischer Domäne - non-kritischer Dom. 3
Sensitivitäts-analysen: Bei hoher Heterogenität a) Ausschluss von Ausreißern, b) Ausschluss von Studien mit hohem RoB (siehe Hauptergebnisse)
Weiterhin a priori geplante Subgruppenanalysen (siehe Hauptergebnisse)
Publikations-bias: Visuelle Prüfung der Funnel-Plots, keine Statistische Prüfung da k<10 in allen MAs
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1a |
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Faller et al. 2013: "Effects of Psycho-Oncologic Interventions on Emotional Distress and Quality of Life in Adult Patients with Cancer: Systematic Review und Meta-Analysis."13
Eingeschlossene Primärstudien: 198 RCTs
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MA
Suchzeitraum: May 2013
Datenbanken: CENTRAL Medline PsycInfo
Einschluss-kriterien: P: erwachsene Krebspatienten I: psychoonkologische Interventionen C: Aufmerkamkeits-Placebo, TAU/UC O: Distress, QoL, Depressivität, Angst S: RCTs
198 RCTS, N=22238 Patientinnen (218 Vergleiche in MA)
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RCTs
Gemischte Krebsdiagnosen (80) Brustkrebs (78) Prostatakarz. (8) Gynekologisch (6) Melanom (5) Hematologischer Krebs (4) Andere (12) Nicht angegeben (5)
Geschlecht: Median 82% weiblich
Alter: Median 54 Jahre
Länder : USA (107) UK (18) Australien (12) Kanada (10) Schweden (9) Niederlande (7) Weitere (35)
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Inhalte: Psychotherapie Einzel (55) Gruppe (42) Paar (10) Psychoedukation (19) Entspannungsverfahren (46) Einfache Informaationsgabe (23) Andere (12)
davon Einzel (119) Gruppe (66) Paar (8) Nicht angegeben (5)
Dauer/Frequenz/ Länge: 1-35 Sitzungen, Median 6 Sitzungen, Über 1-730 Tage, Median 42 Tage
Kontrollgruppen: TAU/UC Aufmerksamkeitskontrolle |
Primäre Endpunkte: 1. Distress 2. gesundheitsbezogene QoL 3. Depressivität 4. Angst |
1. Distress à Gesamteffekt Post-Intervention: 77 RCTs, N=? I2 = 73%; SMD=0.29 [0.20, 0.37, p <.001> Follow Up ≤6 Monate: 58 RCTs, N=? I2 = 56%; SMD=0.17 [0.09, 0.24, p <.001> Follow Up >6 Monate: 39 RCTs, N=? I2 = 32%; SMD=0.10 [0.04, 0.1, p =.003]
à Einzel-psychotherapie Post-Intervention: 18 RCTs, N=? I2 = 88%; SMD=0.48 [0.22, 0.74, p =.002] Follow Up ≤6 Monate: 17 RCTs, N=? I2 = 67%; SMD=0.18 [0.02, 0.35, p=.028] Follow Up >6 Monate: 10 RCTs, N=? I2 = 0%; SMD=0.08 [–0.03, 0.19, p =.15]
à Gruppen-psychotherapie Post-Intervention: 19 RCTs, N=? I2 = 75%; SMD=0.23 [0.05, 0.42, p =.014] Follow Up ≤6 Monate: 16 RCTs, N=? I2 = 34%; SMD=0.03 [–0.09, 0.15, p=.62] Follow Up >6 Monate: 15 RCTs, N=? I2 = 53%; SMD=0.15 [0.01, 0.29, p =.040]
2. QoL à Gesamteffekt Post-Intervention: 66 RCTs, N=? I2 = 78%; SMD=0.26 [0.15, 0.37, p <.001> Follow Up ≤6 Monate: 47 RCTs, N=? I2 = 65%; SMD=0.22 [0.12, 0.33, p <.001> Follow Up >6 Monate: 27 RCTs, N=? I2 = 50%; SMD=0.18 [0.07, 0.28, p <.001>
à Einzel-psychotherapie Post-Intervention: 23 RCTs, N=? I2 = 89%; SMD=0.47 [0.17, 0.77, p =.002] Follow Up ≤6 Monate: 16 RCTs, N=? I2 = 67%; SMD=0.38 [0.18, 0.57, p<.001> Follow Up >6 Monate: 9 RCTs, N=? I2 = 70%; SMD=0.37 [0.09, 0.64, p =.009]
à Gruppen-psychotherapie Post-Intervention: 14 RCTs, N=? I2 = 45%; SMD=0.14 [0.00, 0.28, p =.047] Follow Up ≤6 Monate: 10 RCTs, N=? I2 = 68%; SMD=0.05 [–0.19, 0.29, p=.69] Follow Up >6 Monate: 9 RCTs, N=? I2 = 16%; SMD=0.02 [-0.13, 0.17, p =.81]
3. Depressivität à Gesamteffekt Post-Intervention: 72 RCTs, N=? I2 = 56.5%; SMD=0.33 [0.25, 0.41, p <.001> Follow Up ≤6 Monate: 40 RCTs, N=? I2 = 40.8%; SMD=0.2 [0.11, 0.28, p <.001> Follow Up >6 Monate: 26 RCTs, N=? I2 = 47.1%; SMD=0.14 [0.05, 0.24, p =.002]
à Einzel-psychotherapie Post-Intervention: 22 RCTs, N=? I2 = 51.6%; SMD=0.35 [0.21, 0.49, p =.002] Follow Up ≤6 Monate: 14 RCTs, N=? I2 = 1.3%; SMD=0.13 [0.02, 0.24, p=.024] Follow Up >6 Monate: 10 RCTs, N=? I2 = 40.6%; SMD=0.14 [–0.02, 0.3, p =.1]
à Gruppen-psychotherapie Post-Intervention: 15 RCTs, N=? I2 = 52%; SMD=0.48 [0.29, 0.67, p <.001> Follow Up ≤6 Monate: 9 RCTs, N=? I2 = 19%; SMD=0.21 [0.06, 0.37, p=.006] Follow Up >6 Monate: 5 RCTs, N=? I2 = 10%; SMD=0.28 [0.1, 0.45, p =.002]
4. Angst à Gesamteffekt Post-Intervention: 74 RCTs, N=? I2 = 60%; SMD=0.38 [0.29, 0.46, p <.001> Follow Up ≤6 Monate: 38 RCTs, N=? I2 = 73%; SMD=0.34 [0.2, 0.47, p <.001> Follow Up >6 Monate: 15 RCTs, N=? I2 = 33%; SMD=0.17 [0.06, 0.28, p =.003]
à Einzel-psychotherapie Post-Intervention: 15 RCTs, N=? I2 = 62%; SMD=0.49 [0.29, 0.68, p <.001> Follow Up ≤6 Monate: 11 RCTs, N=? I2 = 47%; SMD=0.33 [0.14, 0.52, p <.001> Follow Up >6 Monate: 10 RCTs, N=? I2 = 0%; SMD=0.07 [–0.07, 0.22, p =.3]
à Gruppen-psychotherapie Post-Intervention: 16 RCTs, N=? I2 = 47%; SMD=0.44 [0.26, 0.62, p <.001> Follow Up ≤6 Monate: 6 RCTs, N=? I2 = 4%; SMD=0.22 [0.07, 0.38, p=.006] Follow Up >6 Monate: 3 RCTs, N=? I2 = 53%; SMD=0.46 [0.15, 0.76, p =.003]
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Nicht berichtet |
Primärstudien: RCTs mit low RoB SB: 51 PB: kA DB: kA AB: 122 RB: 141 OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2, 7, 13 non-kritischer Dom. 3, 10,
Sensitivitäts-analysen: Bei hoher Heterogenität (l²>70%) Ausschluss vjew. einer Studie aus MA & Moderatorenanalysen (u.A. Alter, Tumorart)
Weiterhin a priori geplante Subgruppenanalysen (siehe Hauptergebnisse)
Publikations-bias: Visuelle Prüfung der Funnel-Plots
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1a- |
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Tang et al. 2020: "The Effects of Cognitive-Behavioral Stress Management for Breast Cancer Patients: A Systematic Review and Meta-analysis of Randomized Controlled Trials."1
Eingeschlossene Primärstudien: Antoni 2001, 2006, 2006, 2009, 2012, 2016 Carpenter 2014 Crues 2001 Eaton 2011 Groarke 2012 Lechner 2014 McGregor 2004 Phillips 2008, 2011 Stagl 2012, 2015, 2015 Vargas 2014
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SysRev / MA (nicht für relevante Outcomes)
Suchzeitraum: Bis November 2017
Datenbanken: CENTRAL CINHAL PubMed Medline Embase ScienceDirect PsycInfo
Einschluss-kriterien: P: diagn. Mamma-Ca I: CBSM C: - O: - S: RCTs
Studien mit "high risk of bias" ausgeschlossen!
18 RCTS, N=2564 Patienten
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RCTs
Mamma-Ca
Geschlecht: 100% weiblich
Mittleres Alter: 31 - 73
Länder : USA (17) Irland (1) |
Inhalte: 16x CBSM im Gruppensetting, face-to-face 2x web-basiertes CBSM
Dauer/Frequenz/ Länge: 1,5 – 3 Stunden meist wöchentlich 5 – 20 Wochen
Kontrollgruppen: 11x eintägige Edukation 4x Warteliste 3x sonstiges |
Primäre Endpunkte: 1. Stresserleben 2. Aktuelle Stimung 3. Serum Cortisol
Sekundäre Endpunkte: 4. Angst 5. Depressivität 6. Sinnfindung und positiver Affekt 7. Distress, Stimmungs-beeinträchtigung, "Thought Avoidance". Intrusionen, negativer Affekt 8. Selbstwirksamkeitserleben 9. Physiologische und soziale Indikatoren
Verwendete Messinstrumente: Angst HAMA HADS
Depressivität CES-D HADS
Distress ABS Einzelitems
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1. Angst 2/3 Studien zeigen sign. stärkere Reduktion von Angst in CBSM-Gruppe
2. Depressivität 4/6 Studien zeigen sign. stärkere Reduktion von Depressiviät in CBSM-Gruppe
3. Distress 1/2 Studien zeigen sign. stärkere Reduktion von Distress in CBSM-Gruppe
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Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 1 PB: 0 DB: 9 AB: 18 RB: 18 OB: all unclear
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7,11,15 non-kritischer Dom. 1,3,14
Keine Metaanalysen für relevante Effekte durchgeführt. |
1a- |
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Beatty et al. 2018: "A systematic review of psychotherapeutic interventions for women with metastatic breast cancer: Context matters."15
Eingeschlossene Primärstudien: Classen 2001 Butler 2009 Giese-Davis 2002 Spiegel 2007 Goodwin 2001 Bordeleau 2003 Kissane 2007 Spiegel 1981, 1989, 1993 Cunningham 1998 Edmonds 1999 Edelman 1999a, b Laidlaw 2005 Aranda 2006 Arathuzik 1994 Savard 2006 Scholten 2001 Given 2008 Gotay 2007 Low 2010 Mosher 2012
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SysRev
Suchzeitraum: Bis Mai 2016
Datenbanken: Medline PsycInfo CINAHL SCOPUS
Einschluss-kriterien: P: erwachsene Brustkrebs-patientinnen (metastasiert oder rezidivierend) I: psychothera-peutische Intervention C: - O: u.a. Distress, QoL, somatische Symptome S: RCTs
15 RCTS, N=1638 Patientinnen
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RCTs
Mamma-Ca, metastasiert oder rezidivierend
Geschlecht: 100% weiblich
Mittleres Alter: ~50 - 61
Länder : USA (7) Kanada (3) Australien (3) Österreich (1) UK (1)
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Inhalte: SEGT: Supportiv-expressive Gruppentherapie (2) CBT (5) SEGT/CBTcombi (1) "expressive writing" (2) Hypnose (1) Telefonberatung (2) Pflegegeführte Beratungsge-spräche (1)
davon Einzel (4) Gruppe (7) "low intensity" (4) àinkl. Telefon-beratung (2) und "expressive writing" (2)
Dauer/Frequenz/ Länge: 80min – 78 Stunden
Kontrollgruppen: "Attention control" TAU/UC Warteliste Alternative Behandlung |
Primäre Endpunkte: 1. Überleben 2. Distress 3. Coping 4. QoL 5. Schmerz 6. Fatigue 7. Schlafstörungen
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1. Distress à Gesamteffekt 8/13 RCTs zeigen sign. Reduktion auf min. einem Distress-Outcome à Gruppe: 6/7 RCTs à Einzel: 1/2 RCTs à "low intensiy": 1/4 RCTs
2. QoL à Gesamteffekt 1/6 RCTs zeigen sign. Reduktion auf min. einem QoLOutcome à Gruppe: 1/3 RCTs à Einzel: 0/3 RCTs
3. Schmerz à Gesamteffekt 4/5 RCTs zeigen sign. Reduktion auf min. einem Schmerz-Outcome à Gruppe: 3/3 RCTs à Einzel: 1/1 RCTs à "low intensiy": 0/1 RCTs
4. Fatigue à Gesamteffekt 1/5 RCTs zeigen sign. Reduktion auf min. einem Fatigue-Outcome à Gruppe: 1/2 RCTs à Einzel: 0/1 RCTs à "low intensiy": 0/2 RCTs |
Keine SUEs berichtet. |
Primärstudien: RCTs mit low RoB SB: 9 PB: - DB: 2 AB: 7 RB: 9 OB: 5
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 4, 7 non-kritischer Dom. 1,3,10,14,16
Sensitivitäts-analysen: -
Publikationsbias: Nicht diskutiert
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1a |
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Larkin et al. 2014: "Managing cancer-related fatigue in men with prostate cancer: a systematic review of non-pharmacological interventions."14
Eingeschlossene Primärstudien: 8 davon 3 "psychologische Interventionen":
Badger 2011 Goedendrop 2010 Epsie 2008
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SysRev
Suchzeitraum: 1990 – März 2012
Datenbanken: Pubmed CINAHL Embase PsycINFO CENTRAL PsychExtra SIGLE Australien New Zealand Clinical Trials Registy Clinicaltrials.gov ICTRP EU Clinical Trials Register MedNar
Einschluss-kriterien: P: Erwachsene Prostatakrebs-patienten I: non-pharmakologische Intervention u.a. Edukation, CBT C: andere non-pharmakologische Interventionen, TAU/UC O: Fatigue S: RCTs
8 RCTS
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RCTs
Prostata-Ca
Geschlecht: 100% männlich
Alter: Zw. 46 - 86
Länder : USA (2) Kanada (2) UK (2) Niederlande (1) Unklar (1)
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Inhalte: CBT-basiert (2) Edukation (2) à Goedendrop 2010 sowohl CBT als auch Edukation Sport- und Bewegungs-angebote (5)
Dauer/Frequenz/ Länge: 5-10 Wochen, meist stündliche Termine (für relevante Interventionen)
Kontrollgruppen: TAU/UC |
Primäre Endpunkte: 1. Fatigue
Verwendete Messinstrumente: Fatigue MFI FACT-F FSS FSI PFS-Revised CIS
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1. Fatigue à CBT in 2/2 Studien effektiv zur Reduktion von Fatigue
à Edukation in 1/2 Studien effektiv zur Reduktion von Fatigue
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SUEs in einer Primärstudie berichtet à beziehen sich auf Sport- und Bewegungs-angebot |
Primärstudien: JBI Critical Appraisal Checklist RCTs mit low RoB SB: 4 PB: 0 DB: 3 AB: 5 RB: nicht erfasst OB: nicht erfasst
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,9,13, non-kritischer Dom. 3,5,6,10,14,16
Sensitivitäts-analysen: -
Publikationsbias: Nicht diskutiert
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Einzelpsychotherapie RCTs (2015 – 2020)
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Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Patienten-merkmale |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Finanzierung / Conflict of Interest |
Methodische Bemerkungen |
Evidenzklasse |
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Unterstützende Evidenz (14/21) |
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Balck et al., 2019: A randomized control trial of problem-solving training (PST) for hematopoietic stem cell transplant (HSCT) patients: Effects on anxiety, depression, distress, coping and pain |
RCT, offen, prospektiv, monozentrisch, 2 Arme
Randomisiert: N=95 Post-Intervention: N=67 Follow-Up: N=49
Wahrscheinlich ITT-Analyse ohne Imputation; Ausgewertet: N= 67 (Post-Intervention), 49 (Follow-Up)
Land: Deutschland |
Krebspatienten mit bevorstehender Stammzelltransplantation
Geschlecht: 37,9% weiblich
Alter: 19-72 Mittelwert: 52,58 |
Arm A: NR=46 NP=31 NFU=21 Problemlösetraining (problem-solving training (PST)), fünf 1h-stündige individuelle Sitzungen, eine Sitzung vor Transplantation, die anderen 4 danach (Tag 2, 4, 7, 9 nach Transplantation)
Arm B: NR=49 NP=36 NFU=28 CAU |
Erhebungszeitpunkte Baseline Post-Intervention (10-12 Tage) Follow-Up (2 Wochen)
Primäre Endpunkte: 1. Depressivität (HADS-D) 2. Angst 3. Psychische Belastung (SCL-K-9) 4. Schmerz (QoP) 5. Allgemeiner Distress (NCCN DT)
Sekundäre Endpunkte: 1. Problemlöse-Skills (SPSI-R) 2. Soziale Unterstützung (Subskala von COPE) 3. Coping (COPE) |
Mean-Change von Baseline zu jew. MZP
1. Depressivität à PST versus CAU Post-Intervention: Keine sign. Gruppenunterschiede
Follow-Up: Keine sign. Gruppenunterschiede
2. Angst: à PST versus CAU: Post-intervention: Sign. Gruppenunterschiede zugunsten von PST (Eta2=.13)
Follow-Up: Sign. Gruppenunterschiede zugunsten von PST (Eta2=.13)
3. Psychische Belastung: à PST versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von PST (weniger Verschlechterung in PST; Eta2=.23)
Follow-Up: Keine sign. Gruppenunterschiede
4. Schmerz: à PST versus CAU Post-Intervention: Sign. Gruppenunterschiede zugunsten von PST (geringere Verschlechterung in PST; Eta2=.29)
Follow-Up: Sign. Gruppenunterschiede zugunsten von PST (geringere Verschlechterung in PST; Eta2=.28)
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Arm A: SUEs: 1/46 UEs: 4/46
Arm B: SUEs =/49 UEs: 8/49 |
Deutsche Jose Carreras Leukämie-Stiftung e.V.
Keine Angabe zu COI
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Risk of Bias
SB1: high SB2: unclear PB: high DB: high AB: unclear RB: unclear
Keine Fallzahlplanung |
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Bao et al., 2019: Intensive patient’s care program reduces anxiety and depression as well as improves overall survival in de novo acute myelocytic leukemia patients who underwent chemotherapy: a randomized, controlled study |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N= 220 Mid-Intervention1: N=kA Mid-Intervention2: N=kA Mid-Intervention3: N=kA Post-Intervention: N=178
ITT-Analyse mit Imputation (LOCF); Ausgewertet: N=220
Land: China 2014-2016 |
Leukämie-PatientInnen während der Chemotherapie
Geschlecht; 49,1% weiblich
Alter: Mittelwert: 43,85 |
Arm A: NR=110 NM=kA NM2=kA NM3=kA NP=92 Intensive Patient’s Care Program (IPCP), über 12 Monate, Mix aus Edukation (Manual + wöchentliche 60min Sitzungen in den ersten 3 Monaten), psychische/psychologische Unterstützung (alle zwei Wochen von Monat 4-9, je 60min), Telefon-Counseling (alle zwei Wochen von Monat 10-12, je ca. 25-30min)
Arm B: N=110 N=kA N=kA N=kA N=86 CAU
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Erhebungszeitpunkte Baseline Mid-Intervention1 (3 Monate Post-Baseline) Mid-Intervention2 (6 Monate Post-Baseline) Mid-Intervnetion3 (9-Monate Post-Baseline) Post-Intervention
Primäre Endpunkte: 1. Depressivität (HADS-D + SDS) 2. Angst
Sekundäre Endpunkte: 1. Event-free survivals (EFS) 2. Overall survival (OS) |
1. Depressivität à IPCP versus CAU: Post-Intervention: HADS-D: sign. Gruppenunterschiede zugunsten von IPCP auf HADS-D UND SDS
2. Angst: à IPCP versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von IPCP auf HADS-A, gemischte Ergebnisse bzgl. SAS (Score sign. niedriger Post-Intervention bei IPCP, aber Gesamtveränderung von Baseline zu Post-Intervention nicht sign. unterschiedlich) |
Nicht berichtet |
Keine Angaben zur Finanzierung
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: unclear
Keine Fallzahlplanung |
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Burm et al., 2019: Long-term efficacy and cost-effectiveness of blended cognitive behavior therapy for high fear of recurrence in breast, prostate and colorectal Cancer survivors: follow-up of the SWORD randomized controlled trial |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=88 Post-Intervention: N=82 Follow-Up1: N=82 Follow-Up2: N=69
Modifizierte ITT-Analyse; ausgewertet: N=88
Land: Niederlande 2014-2016 |
Krebsüberlebende (Brust, Prostata und Darm), mit hoher Rezidivangst (CWS über 14), Krebsbehandlung abgeschlossen vor min. 6 Monaten und max. 5 Jahren
Geschlecht: 53,4% weiblich
Alter: Mittelwert: 58,83 |
Arm A: NR=45 NP=43 NFU1=39 NFU2=38 Blended KVT (bKVT), 5 individuelle 1h face-to-face Sitzungen 8Sitzungen 1,2,3,5,8) + drei 15-min e-konsultatiotnen (Sitzungen 4,6,7), über 3 Monate, Mix aus PE, kognitive Umstrukturierung, Verhaltensmodifikation, 3 Monate nach Interventionsende eine Booster-Sitzung (1h, face-to-face)
Arm B: NR=43 NP=39 NFU1=43 NFU2=32 CAU
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Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up1 (24 Wochen) Follow-Up2 (48 Wochen)
Primäre Endpunkte: 1. Rezidivangst (CWS)
Sekundäre Endpunkte: 2. Schwere der Rezidivangst (FCRI severity subscale) 3. Krebsbezogene Belastung (IES) 4. Psychische Belastung (HADS) 5. Depressivität (HADS-D) 6. Angst (HADS-A) 7. Fatigue (CIS-8R) 8. QoL (global) (EORTC QLQ-C30) 9. QUALYs |
1. Rezidivangst à bKVT versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up1: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up2: Sign. Gruppenunterschiede zugunsten von bKVT
2. Psychische Belastung à bKVT versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up1: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up2: Keine sign. Gruppenunterschiede
3. Depressivität à bKVT versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up1: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up2: Keine sign. Gruppenunterschiede
4. Angst à bKVT versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up1: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up2: Sign. Gruppenunterschiede zugunsten von bKVT
5. Fatigue à bKVT versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up1: Keine sign. Gruppenunterschiede
Follow-Up2: Keine sign. Gruppenunterschiede
6. QoL (global): à bKVT versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up1: Sign. Gruppenunterschiede zugunsten von bKVT
Follow-Up2: Keine sign. Gruppenunterschiede
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keine |
Dutch Cancer Society
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: low
PatientInnen in CAU hatten deutlich mehr anderweitigen psychosozialen support als PatientInnen in bKVT, könnte Ergebnisse verzerrt haben
Geplante Fallzahl (N=104) nicht erreicht (Fallzahlplanung nur im Studienprotokoll erwähnt, nicht im Paper selbst) |
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Fatehi et al., 2019: The effects of psychosexual counseling on sexual quality of life and function in Iranian breast cancer survivors: a randomized controlled trial |
RCT, offen, prospektiv, monzentrisch, 2 Arme
Randomisiert: N=118 Post-Intervention: N=100 (kA) Follow-Up: N=100
Kein ITT-Ansatz; ausgewertet: N=100
Land: Iran 2015 |
Brustkrebspatientinnen, Stage I-III, verheiratet, keine Hormontherapie, mit Mastektomie-Erfahrungen, keine Brustrekonstruktion
Geschlecht: 100% weiblich
Alter: Mittelwert: ca. 44,3 |
Arm A: NR=59 NP=51 (kA) NFU=51 Psychosexuelle Beratung (PSB), sechs wöchentliche Sitzungen, 90-120min,
Arm B: NR=59 NP=49 (kA) NFU=49 WL |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up (12 Wochen)
Primäre Endpunkte: 1. Sexuelle Funktion (FSFI) 2. Sexuelle QoL (SQOL-F) 3. Sexuelle Zufriedenheit (Larson ISS) |
1. Sexuelle Funktion: à PSB versus WL: Follow-Up: Sign. Gruppenunterschiede zugunsten von PSB
2. Sexuelle QoL: à PSB versus WL: Follow-Up: Sign. Gruppenunterschiede zugunsten von PSB
3. Sexuelle Zufriedenheit à PSB versus WL: Follow-Up: Keine sign. Gruppenunterschiede
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Nicht berichtet |
Shahroud University of Medical Sciences and granted approval by Mazandaran University of Medical Sciences
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: unclear RB: high
Post-Intervention erhoben, aber nicht berichtet
Geplante Fallzahl (N=120) nicht erreicht |
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Peoples et al., 2019: Cognitive Behavioral Therapy for Insomnia Reduces Depression in Cancer Survivors |
RCT, halb-blind, prospektiv, multizentrisch, 4 Arme (davon 2 KVT-I und 2 Non-KVT-I, hier jeweils zusammengefasst)
Randomisiert: N=96 Post-Intervention: N=73 Follow-Up: N=67
Kein ITT-Ansatz; ausgewertet: N=67
Land: USA 2008-2012 |
Krebsüberlebende (69% Brustkrebs),
Geschlecht: 90% weiblich
Alter: Mittelwert: 56 |
Arm A: NR=47 NP=37 NFU=35 KVT-I (kognitiv-behaviorale Therapie gegen Insomnie) + Placebo ODER Armodafinil, 7 wöchentliche Sitzungen, 3 Sitzungen face-to-face (30-60min), 4 Sitzungen telefonisch (15-30min)
Arm B: NR=49 NP=36 NFU=32 Armodafinil ODER Placebo |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up (12 Wochen)
Primäre Endpunkte: 1. Depressivität (PHQ-9) 2. Insomnie (ISI) |
1. Depressivität: à KVT-I versus non-KVT-I: Post-Intervention: Sign. Gruppenunterschiede zugunsten von KVT-I (d= -.62); sign. mehr klinische Verbesserung in KVT-I und geringere Rate an Depressiven in KVT-I
Follow-Up: Sign. Gruppenunterschiede zugunsten von KVT-I, sign. mehr klinische Verbesserung und geringere Rate an Depressiven in KVT-I
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Keine berichtet |
National Cancer Institute grants, National Center for Advancing Translational Sciences grant TL1, Study medication, armodafinil, was provided by Teva Pharmaceuticals, USA,
Autor Perlis berichtet COI; die anderen Autoren haben laut Angaben keine COI |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Sekundäranalyse
Eigentlich gab es 4 Gruppen, aber Analyse wurde so durchgeführt: PatientInnen die KVT-I erhalten haben vs. Die, die kein KVT-I erhalten haben (eigentlich KVT-I noch unterteilt in Placebo-Medikament und richtiges Medikament; non-KVT-I noch unterteilt in Placebo und richtiges Medikament)
Sekundäre Analyse von Roscoe JA, Garland SN, Heckler CE, et al. Randomized placebo-controlled trial of cognitive behavioral therapy and armodafinil for insomnia after cancer treatment. J Clin Oncol. 2015;33(2):165–171.
Geplante Fallzahl (N=96) nicht erreicht (Power-Analyse in anderem Paper der primären Analyse beschrieben, s.o.) |
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Al-Sulaiman et al., 2018 : Exploring the effectiveness of crisis counseling and psychoeducation in relation to improving mental well-being, quality of life and treatment compliance of breast cancer patients in Qatar |
RCT, prospektiv, offen, monozentrisch, 3 Arme
Randomisiert: N= 201 Post-Intervention: N = kA Follow-Up : N = kA
kA zur Analyse-Technik ; ausgewertet : kA
Land : Qatar 2012-2015 (Rekrutierung) |
Brustkrebspatientinnen, frühe Stadien (I-III)
Geschlecht : 100% weiblich
Alter : 30-50+ Mittelwert : kA |
Arm A : NR = 67 NPI = kA NFU = kA
PE, Einzel, 6x 60-90min Sitzungen über 12 Wochen
Arm B : NR = 67 NPI = kA NFU = kA
Krisenberatung (KB), one-to-one, sechs 60-90min Sitzungen über 12 Wochen
Arm C : NR = 67 NPI = kA NFU = kA
CAU
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Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (72 Wochen)
Primäre Endpunkte: 1. Depressivität (DASS-21) 2. Angst (DASS-21) 3. Stress (DASS-21) 4. QoL (global) (EORTC QLQ-C30) |
1. Depressivität à PE versus KB versus CAU : Post-Intervention: Sign. Gruppenunterschiede zugunsten von PE und KB jeweils verglichen mit CAU; sign. Gruppenunterschiede zugunsten von PE verglichen mit KB
Follow-Up : Sign. Gruppenunterschiede zugunsten von PE und KB jeweils verglichen mit CAU; keine Unterschiede zwischen PE und KB
2. Angst: à PE versus KB versus CAU : Post-Intervention: Sign. Gruppenunterschiede zugunsten von PE und KB jeweils verglichen mit CAU ; keine Unterschiede zwischen PE und KB
Follow-Up : Sign. Gruppenunterschiede zugunsten von PE und KB jeweils verglichen mit CAU; keine Unterschiede zwischen PE und KB
3. QoL (global): à PE versus KB versus CAU : Post-intervention : Sign. Gruppenunterschiede zugunsten von PE und KB, jeweils verglichen mit CAU ; keine Unterschiede zwischen PE und KB
Follow-Up : Sign. Gruppenunterschiede zugunsten von PE und KB für Subskala emotional functioning ; keine Unterschiede zwischen PE und KB |
Nicht berichtet |
Keine Angabe zur Finanzierung
Laut Angaben keine COI
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Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: unclear RB: low
Keine Fallzahlplanung
„While this may be considered quite a small sample, the maximum sample size was limited by the overall number of patients in the country”
Follow-Up eigtl. für 6 Monate Post-Intervention geplant
"Another potential limitation of this study is that the assessment of the long-term effects of the crisis counseling and psychoeducation interventions was not achieved at 6 months as planned, but was delayed until 18 months after the interventions. This was because most patients were unavailable at the 6-month mark, whether due to extended travel commitments or because they simply did not respond to requests from the research assistants." |
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Aminnasab et al., 2018: Effectiveness of Solution-Focused Brief Therapy (SFBT) on Depression and Perceived Stress in Patients with Breast Cancer |
RCT, offen, prospektiv, monozentrisch, 2 Arme
Randomisiert: N=30 Post-Intervention: N=kA Follow-Up: N=kA
kA zu Analyse-Methode; Ausgewertet. N=30
Land: Iran November 2015-Februar 2016
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Brustkrebspatientinnen, Stages I-III,
Geschlecht. 100% weiblich
Alter: 20-45 Mittelwert: nicht berichtet(?) |
Arm A: NR=15 NP=kA NFU=kA Solution-Focused Brief Therapy (SFBT), eine Sitzung wöchentlich a 2h, über 8 Wochen
Arm B: NR=15 NP=kA NFU=kA CAU |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up (4 Wochen)
Primäre Endpunkte: 1. Stress (PSS) 2. Depressivität (CES-D) |
1. Depressivität: à SFBT versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von SFBT
Follow-Up: Sign. Gruppenunterschiede zugunsten von SFBT
Effektstärke der Zeit x Gruppen-Interaktion: ηp2=.88
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Nicht berichtet |
Keine Angaben |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: unclear RB: low
Studie als semi-experimentell bezeichnet
Keine Fallzahlplanung (keine Power-Analyse):
In order to calculate the sample size, according to the fact that the proper sample size was 15 people for each group (15), the sample size was selected equal to 15 people for each group.
Kein Flow-Diagramm, keine Angabe zu Attrition oder Compliance
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Desautels et al., 2018: Treatment of Depressive Symptoms in Patients With Breast Cancer: A Randomized Controlled Trial Comparing Cognitive Therapy and Bright Light Therapy |
RCT, offen, pospektiv, monozentrisch, 3 Arme
Randomisiert: N=62 Post-Intervention: N=57 Follow-Up1: N=56 Follow-Up2: N=54
ITT-Ansatz ohne Imputation; ausgewertet: N=57 (Post); N=54(Follow-Ups)
Land: Kanada 2011-2015 |
Brustkrebspatientinnen, Stage I-III, erhöhte Depressivitätswerteà Score über 7 bzw. 14 bei HADS-D bzw. BDI-II (aber Depressionsdiagnose nach SCID Ausschlusskriterium)
Geschlecht: 100% weiblich
Alter: 33-75 Mittelwert: 51,7 |
Arm A: NR=25 NP=25 NFU1=24 NFU2=24 Kognitive Therapie (KT), über 8 Wochen, wöchentliche Sitzungen à 60min,
Arm B: NR=26 NP=22 NFU1=22 NFU2=22 Bright Light Therapy (BLT), über 8 Wochen, sollten sich jeden Morgen (vor 10 Uhr) 30min mit 10000 LUX-Lampe bestrahlen
Arm C: NR=11 NP=10 NFU1=8 NFU2=8 WL, nach 8 Wochen dann randomisiert zu KT oder BLT zugeteilt |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up1 (12 Wochen) Follow-Up2 (24 Wochen)
Primäre Endpunkte: 1. Depressivität (HADS-D & BDI-II & HDRS) |
1. Depressivität (HADS-D) à KT versus BLT versus WL Post-Intervention: Sign. Gruppenunterschiede zugunsten von KT (within d=-1,6) und BLT (within d=-1,5) verglichen mit WL (within d=-0,5),
à KT vs BLT Follow-Up1: Keine sign. Gruppenunterschiede
Follow-Up2: Keine sign. Gruppenunterschiede
2. Depressivität (BDI-II) à KT vs BLT vs WL Post-Intervention: Sign. Gruppenunterschiede zugunsten von KT (within d=-1,7) verglichen mit BLT (within d=-1,1) und WL (within d=-0,7; BLT keine sign. Unterschiede zu WL
à KT vs BLT Follow-Up1: Sign. Gruppenunterschiede zugunsten von KT
Follow-Up2: Sign. Gruppenunterschiede zugunsten von KT
3. Depressivität (HDRS) à KT vs BLT vs WL Post-Intervention: Sign. Gruppenunterschiede zugunsten von KT verglichen mit BLT, aber keine sign. Gruppenunterschiede von KT (within d=-0,7) oder BLT (within d=-0,3) gegenüber WL (within d=-0,2)
à KT vs BLT Follow-Up1: Keine sign. Gruppenunterschiede
Follow-Up2: Keine sign. Gruppenunterschiede
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Nicht berichtet |
training awards from the Canadian Institutes of Health Research, the Psychosocial Oncology Research Training program, and the CHU de Québec—Université Laval Research Center, held by the first author
keine Angaben zum COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: unclear
Post-Treatment: Vergleich zwischen KT, BLT und WL; bei FUs nur Vergleich zwischen KT und BLT (WL wurde nach 8 Wochen/Post-Treatment zu KT oder BLT randomisiert zugeordnet)
Sign. mehr Chemotherapie und höhere Krebsstadien in KT; mehr saisonale Depressionen in BLT
Geplante Fallzahl (N=60) nicht erreicht |
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Kim et al., 2018: A psychological intervention programme for patients with breast cancer under chemotherapy and at a high risk of depression: A randomised clinical trial |
RCT, offen, prospektiv, monozentrisch, 2 Arme
Randomisiert: N=60 Post-Intervention: N=55 Follow-Up: N=53
kA ob ITT; Ausgewertet: N=kA
Land: Südkorea |
Brustkrebspatientinnen, Stage I-III, während der Chemotherapie, erhöhtes Risiko für Depression (Score über 16 auf CES-D)
Geschlecht: 100% weiblich
Alter: 30-69 Mittelwert: 48 |
Arm A: NR=30 NP=29 N=29 Nurse-led psychologisches Beratung (NLPB), sowohl face-to-face als auch telefonisch, 7 wöchentliche Sitzungen, je 30-60min,
Arm B: NR=30 NP=26 N=24 CAU |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up (3 Wochen)
Primäre Endpunkte: 1. Angst (HADS-A) 2. Depressivität (HADS-D) 3. QoL global (EROTC QLQ-C30) 4. Mood disturbances (K-POMS-B) 5. Körperliche Symptome (u.a. Fatigue, Übelkeit, Schmerzen; EROTC QLQ-C30) |
1. Angst à NLPB versus CAU Keine sign. ZeitxGruppe-Interaktion, sign. Verbesserung in beiden Gruppen
2. Depressivität à NLPB versus CAU Sign. ZeitxGruppe-Interaktion zugunsten von NLPB
3. QoL à NLPB versus CAU Keine sign. ZeitxGruppe-Interaktion, keine sign. Verbesserung
4. Fatigue à NLPB versus CAU Sign. ZeitxGruppe-Interaktion zugunsten von NLPB
5. Übelkeit à NLPB versus CAU Sign. ZeitxGruppe-Interaktion zugunsten von NLPB
6. Schmerzen à NLPB versus CAU Keine sign. ZeitxGruppe-Interaktion
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Keine berichtet |
Keine Finanzierung, da Teil einer Dissertation
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: unclear RB: unclear
Geplante Fallzahl (N=44) erreicht |
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Qiu et al., 2018: Effects of cognitive behavioral therapy for depression on improving insomnia and quality of life in Chinese women with breast cancer: results of a randomized, controlled, multicenter trial |
RCT, multizentrisch, offen, prospektiv, 3 Arme
Randomisiert: N=392 Post-Intervention: N=kA Follow-Up: N=356
ITT-Ansatz mit Imputation (LOCF); ausgewertet: N=392
Land: China 2010-2012 |
Brustkrebspatientinnen, Stage I-III
Geschlecht: 100% weiblich
Alter: Mittelwert: 47,06 |
Arm A: NR=98 NP=kA NFU=91 KVT, 9 Sitzungen über 12 Wochen
Arm B: NR=98 NP=kA NFU=90 Selbstfürsorge-Management (SFM; Self-care Management), 9 Sitzungen über 12 Wochen
Arm C: NR=196 NP=kA NFU=175 CAU |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up (12 Wochen)
Primäre Endpunkte: 1. QoL global (FACT-B) 2. Insomnie (AIS) |
1. QoL global: à KVT versus SFM versus CAU: Post-Intervention: Sign. ZeitxGruppe-Interaktion (ES: (ηp2 =0.137), sign. Gruppenunterschiede zugunsten von KVT sowohl gegenüber SFM als auch CAU; keine sign. Gruppenunterschiede zwischen SFM und CAU
Follow-Up: Sign. Gruppenunterschiede zugunsten von KVT sowohl gegenüber SCM als auch CAU; keine sign. Gruppenunterschiede zwischen SFM und CAU |
Keine berichtet |
National Key Technologies R&D program in the 11th 5-year plan from the Ministry of Science and Technology of the People’s Republic of China
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: low
Sign. Gruppenunterschiede bei Baseline bzgl. Depressivität und Angst (höhere Werte in KVT)à wurde aber statistisch kontrolliert
Keine Fallzahplanung, aber Angabe, dass mit Stichprobe 90% Power erreicht werde konnte um Effekte zu erfassen mit a=.05 |
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Scarpa et al., 2017: Randomized clinical trial of psychological support and sleep adjuvant measures for postoperative sleep disturbance in patients undergoing oesophagectomy |
RCT, prospektiv, monozentrisch, offen, 4 Arme
Randomisiert: N=87 Post-Intervention: N=74
Kein ITT-Ansatz; ausgewertet: N=74
Land: Italien 2013-2016 |
KrebspatientInnen mit operativer Entfernung der Speiseröhre (Ösophagektomie),
Geschlecht: ca. 14,5% weiblich
Alter: Mittelwert: ca. 63,5 |
Arm A: NR=19 NP=16 PSB + adjuvante Schlafmmaßnahmen (Schlafmasken und Ohrstöpsel? Isolierte, ruhige, dunklere Räume) (PSBAM), Behandlung während Krankenhausaufenthalt, PC: 4 Sitzungen, eine 30min bei Aufnahme in KH, 15min ein Tag nach OP, 30min vor Entfernung der Nasensonde, 30min vor Entlassung; je nach Bedarf weitere SItzungen
Arm B: NR=23 NP=19 Nur PSB, während Krankenhausaufenthalt
Arm C: NR=22 NP=19 Nur adjuvante Schlafmaßnahmen (SAM), während Krankenhausaufenthalt
Arm D: NR=23 NP=20 CAU
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Erhebungszeitpunkte Baseline Post-Intervention
Primäre Endpunkte: 1. QoL (EORTC C30-QL2)
Sekundäre Endpunkte: 1. Schlafqualität (PSQI, EORTC C30-SL) 2. Fatigue (EORTC C30-FA) 3. Menge an benötigten Medikamenten 4. Schmerzen (VAS) |
Analyse von Häufigkeiten in Vier-Felder-Tafel (mit/ohne PSB + mit/ohne SAM), Angabe von Odds-Ratio (OR)
1. QoL Post-Intervention: Sign. reduziertes Risiko für QoL-Beeinträchtigung mit PSB vs. ohne PSB (OR=0.23, p=.003)
2. Fatigue: Post-Intervention: Kein sign. reduziertes Risiko für Fatigue-Beeinträchtigung
3. Schmerzen: Post-Intervention: Keine sign. Gruppenunterschiede
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Keine berichtet |
Berlucchi Foundation (Brescia, Italy) to C.C
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: unclear RB: unclear
Geplante Fallzahl (N=64) erreicht |
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Olesen et al., 2016: A person-centered intervention targeting the psychosocial needs of gynecological cancer survivors: a randomized clinical trial |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=165 Post-Intervention: N=158 Follow-Up: N=158
ITT-Ansatz; ausgewertet: N=162
Land: Dänemark 2013-2014 |
Patientinnen mit gynäkologischem Krebs
Geschlecht: 100% weiblich
Alter: 38-63 Mittelwert: ca. 50 |
Arm A: NR=80 NP=73 NFU=73 Personenzentrierte Intervention, 2-4 Pflege-Gespräche über 3 Monate je 1h, basierend auf guided self-determination, auf gynäkologischen Krebs zugeschnitten (GSD-GYN-C)
Arm B: NR=85 NP=85 NFU=85 CAU |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up (24 Wochen)
Primäre Endpunkte: 1. QoL global (QOL-CS)
Sekundäre Endpunkte: 1. Impact of cancer (IOCv2) 2. Selbstbewusstsein (Rosenberg Self-Esteem Scale) 3. Distress (DT) 4. Angst (HADS-A) 5. Depressivität (HADS-D) 6. Unterstützung durch Gesundheitspersonal (HCCQ) 7. Fähigkeit, Rezidivsymptome zu überwachen (eigene Skala)
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1. QoL global à GSD-GYN-C versus CAU Post-Intervention: Sign. Gruppenunterschiede zugunsten von GSD-GYN-C; ABER: nicht mehr sign. nach Berücksichtigung der Baseline-Unterschiede!
Follow-Up: Sign. Gruppenunterschiede zugunsten von GSD-GYN-C; ABER: nicht mehr sign. nach Berücksichtigung der Baseline-Unterschiede!
Ansonsten keine sign. Gruppenunterschiede auf den uns interessierenden Variablen
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Keine berichtet |
The Danish Cancer Society, The Health Foundation, Danish Cancer Research Fund, Juliane Marie Centre and The Research Fund of Rigshospitalet, Copenhagen University Hospital; and The Danish Nurses’ Organization Nursing Research Fund
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: low
Viele „baseline imbalances“ die das Ergebnis verzerrt haben könnten
Geplante Fallzahl (N=160) erreicht |
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Pelekasis et al., 2016: Forming a Stress Management and Health Promotion Program for Women Undergoing Chemotherapy for Breast Cancer: A Pilot Randomized Controlled Trial |
RCT, halb-blind, prospektiv, monozentrisch, 2 Arme
Randomisiert: N=61 Post-Intervention: N=53
Kein ITT-Ansatz; ausgewertet: N=53
Land: Griechenland |
Brustkrebspatientinnen, während der Chemotherapie, Stage I-IV
Geschlecht: 100% weiblich
Alter: Mittelwert: 55,9 |
Arm A: NR=30 NP=25 8-Wochen Stress-Management und Gesundheits-Programm (SMGP), 6 wöchentlich 30min Sitzungen,
Arm B: NR=31 NP=28 AC, 15-min Meeting mit Forschenden, |
Erhebungszeitpunkte Baseline Post-Intervention
Primäre Endpunkte: 1. Gesundheit (10- stufige LS) 2. Nachschlafzeit 3. Dauer bis zum Einschlafen 4. Depressivität (DASS-21) 5. Angst (DASS-21) 6. Stress (DASS-21) 7. Wahrgenommene Kontrollierbarkeit bzg. Gesundheit (HLC) 8. Spirituelles Wohlergehen (SWBS)
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1. Depressivität: à SMGP versus AC: Post-Intervention: Sign. Gruppenunterschiede zugunsten von SMGP (ES r=0.35)
2. Angst: à SMGP versus AC: Post-Intervention: Sign. Gruppenunterschiede zugunsten von SMGP (ES r=0.39)
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Keine berichtet |
Laut Angaben keine Finanzierung
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: high PB: high DB: high AB: high RB: unclear
Pilotstudie
Keine Fallzahlplanung
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Aktas et al., 2015: Effect of Home Care Service on the Sexual Satisfaction of Patients with Gynecologic Cancer |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=70 Post-Intervention: N=70
kA zu Analysemethode; Ausgewertet: N=70
Land: Türkei 2011-2012 |
Patientinnen mit gynäkologischem Krebs (44,35% Eierstockkrebs, 40% Uteruskrebs, 15,65% Gebärmutterhalskrebs), Stage I-III, während Chemo- oder Strahlungstherapie, zum ersten Mal wegen Krebs operiert
Geshlecht: 100% weiblich
Alter: Mittelwert: 49,3 |
Arm A: NR=35 NP=35 Heim-Betreuungs- Service (HBS), Konsulatationen und Betreuung durch Krankenpfleger zuhause (1. Und 12. Woche) sowie die restlichen Wochen 3x/Woche im Krankenhaus
Arm B: NR=35 NP=35 CAU |
Erhebungszeitpunkte Baseline Post-Intervention
Primäre Endpunkte: 1. Sexuelle Funktion (GRISS) 2. Sexuelle Zufriedenheit (GRISS) |
1. Sexuelle Funktion: à HBS versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von HBS
2. Sexuelle Zufriedenheit: à HBS versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von HBS |
Keine berichtet |
Keine Angaben zur Finanzierung Laut Angaben keine COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: low RB: low anscheinend Fallzahlplanung, aber nicht genau beschrieben (keine Power-Analyse berichtet)
kein Flowdiagramm o.ä., keine Atrittion-Rate o.ä. berichtet |
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Keine Hinweise für höhere Wirksamkeit des Treatments (7/21) |
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Arving et al., 2019: Early rehabilitation of cancer patients—An individual randomized stepped‐care stress‐management intervention |
RCT, offen, prospektiv, monozentrisch, 2 Arme
Randomisiert: N=291 Mid-Intervention1: N=276 Mid-Intervention2: N=266 Post-Intervention: N=264 Follow-Up1: N=256 Follow-Up2: N=252
ITT-Analyse (aber nur im online-Anhang; im Paper wahrscheinlich die PP-Analyse berichtet); Ausgewertet und im Paper berichtet: N=250-275 (je nach MZP und Outcome)
Land: Norwegen 2011-2013 |
Krebspatienten (42% Brustkrebs, 43% Prostatakrebs), Stage I-III, während (neo-)adjuvanter/kurativer Therapie
Geschlecht: 47% weiblich
Alter: 22-81 Mittelwert: 61 |
Arm A: N=145 NM1=138 NM2=132 NP=130 NFU1=125 NFU2=123 Stepped-Care Stress-Management (SCSM), KVT-Ansätze, Step 1: 2 Sitzungen, Step 2: nach Bedarf zusätzlich 3-8 Sitzungen, alle Sitzungen ca. 45-60min lang; max. Dauer der Intervention: 26 Wochen
Arm B: NR= 146 NM1=138 NM2=134 NP=134 NFU1=131 NFU2=129 CAU |
Erhebungszeitpunkte Baseline Mid-Intervention1 (6 Wochen Post-Baseline) Mid-Intervention2 (17 Wochen Post-Baseline) Post-Intervention Follow-Up1 (17 Wochen) Follow-Up2 (69 Wochen)
Primäre Endpunkte: 1. Krebsbezogene Stressreaktionen (IES) 2. Psychischer Distress (HADS) 3. Emotionale Reaktivität (ELSS)
Sekundäre Endpunkte: 1. Depressivität (HADS-D) 2. Angst (HADS-A) |
Keine sign. Gruppenunterschiede in relevanten Outcomes
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Nicht berichtet |
Grieg Foundation and the Norwegian Cancer Society
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: unclear RB: high
Geplante Fallzahl (N=256) erreicht |
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Aubin et al., 2019: Cancer!? I don't have time for that: impact of a psychosocial intervention for young adults with cancer |
RCT, offen, prospektiv, monozentrisch, 2 Arme
Randomisiert: N=113 Post-Intervention: N=99 Follow-Up1: N=95
ITT-Analyse mit multipler Imputation (Monte-Carlo) wenn mind. Post-Werte vorlagen Ausgewertet: N=99
Land: Kanada
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KrebspatientInnen (18-39 Jahre), gemischte Diagnosen (haupts. Brust ~25%, Hodgkin Lymphom 18%)
Geschlecht: 78,9% (CAU) und 74,5% (EG) weiblich
Alter: ka Mittelwert: 29,6 (CAU), 30,6 (EG) |
Arm A: N=57 NP=47 NFU1=45 Kurze psychosoziale Intervention für AYACs (EG), 3 Sitzungen, 60min, zweiwöchentlich, 6 Wochen
Arm B: NR= 56 NP=52 NFU1=50 CAU |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up1 (12 Wochen)
Primäre Endpunkte: 1. Angst (HADS-A) 2. Depressivität (HADS-D) 3. Distress (HADS) 4. QoL global (FACT-G) 5. Selbstwirksamkeit mit chronischer Krankheit (CDSES) 6. Selbstwertgefühl mit Sexualität (Sexuality Scale) 7. Belastung durch Sexualität (Sexuality Scale)
Sekundäre Endpunkte: 3. Depressivität (HADS-D) 4. Angst (HADS-A) |
Keine sign. Gruppenunterschiede auf relevanten Endpunkten zu keinem Erhebungszeitpunkt
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Nicht berichtet |
Laut Angaben keine COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: unclear RB: unclear
Geplante Fallzahl (N=128) nicht erreicht
t-Tests mit Bonferroni-Adjustierung für max. Power |
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Garcia et al., 2018: The effect of therapeutic listening on anxiety and fear among surgical patients: randomized controlled trial |
RCT, offen, prospektiv, monozentrisch, 2 Arme
Randomisiert/Baseline1: N=50 Baseline2: N=50 Post-Intervention: N=50
kA ob ITT, es haben aber auch alle Teilnehmenden Daten geliefert und Intervention nach Plan abgeschlossen; Ausgewertet: N=50
Land: Brasilien 2014-2015
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DarmkrebspatientInnen vor der OP, Stage I-III
Geschlecht; 56% weiblich
Alter: Mittelwert: 57,5 |
Arm A: NR/B1=25 NB2=25 NP=25 Therapeutisches Zuhören (TZ; Therapeutic Listening), 30min Gespräch ein Tag vor OP
Arm B: NR/B1=25 NB2=25 NP=25 CAU, nur Assessment ein Tag vor OP für 30min (Researcher nicht für komplette 30min anwesend)
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Erhebungszeitpunkte Baseline1 Baseline2 Post-Intervention
Primäre Endpunkte: 1. Angst (STAI) 2. Psychophysiologische Parameter (Speichel-Kortisol, Herzrate, Blutdruck etc.) 3. Angst vor OP (SFQ) |
Keine sign. Gruppenunterschiede |
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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Brazil
Keine Angaben über COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: unclear Geplante Fallzahl (N=50) erreicht |
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Hazard Vallerdand et al., 2018: Improving Functional Status in African Americans With Cancer Pain: A Randomized Clinical Trial |
RCT, offen, prospektiv, monozentrisch, 2 Arme
Randomisiert: N=310 Post-Intervention: N=236 Follow-Up: N=223
ITT-Ansatz; Ausgewertet: N=310
Land: USA |
Afro-amerikanische PatientInnen mit krebsbezogenen Schmerzen (über 4 auf Likert-Skala (0-10)), 68,22% Brust, 39,13% Lunge, 34,11% Mund, 30,1% urogenital, 24,8% gastrointestinal
Geschlecht: 63% weiblich
Alter: Mittelwert: 56,28 |
Arm A: NR=180 NP=130 NFU=122 Power over Pain-Coaching (POP-C), zu Hause durchgeführt, In Woche 2, 4 und 6 Heimbesuche, Telefonate in Woche 3 und 5, Dauer Intervention: 5 Wochen
Arm B: NR=130 NP=106 NFU=101 CAU |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (5 Wochen)
Primäre Endpunkte: 1. Schmerzen (BPI, PPQ) 2. Schmerzbezogene Belastung (DT, MSAS, PPQ) 3. Funktioneller Status (QOL (QoLS ACPA, KPS, BPI, SF12)
Mediatoren: 4. Katastrophisieren von Schmerzen (PCS) 5. Kognitive Kontrolle (SOPA) 6. Pharmakologische Kontrolle (PCS) 7. Erlebte Kontrolle (PPQ, demo)
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1. Schmerzen: à POP-C versus CAU: Post-Intervention: Keine sign. Gruppenunterschiede, sign. Verbesserung in beiden Gruppen (keine sign. ZeitxGruppe-Interaktion)
Follow-Up: Keine sign. Gruppenunterschiede, aber Verbesserung durch Intervention konnte aufrechterhalten werden (keine Verschlechterung oder Verbesserung)
2. Funktioneller Status/QOL à POP-C versus CAU: Post-Intervention: Keine sign. Gruppenunterschiede, sign. ZeitxGruppe Interaktion zugunsten POP-C (ES: .19 (estimate/SD))
Follow-Up: kA ob sign., aber Interventionseffekt wahrscheinlich stabil geblieben
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National Cancer Institute, Michigan Center for Urban African American Aging Research
Nicht klar, ob COI angegeben ist |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
ProbandInnen in POP-C sign. älter und längere Zeit seit Diagnose
Geplante Fallzahl (N=220) erreicht |
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Richardson et al., 2017: A Self-Regulatory Intervention for Patients with Head and Neck Cancer: Pilot Randomized Trial |
RCT, offen, prospektiv, monozentrisch, 2 Arme
Randomisiert: N=64 Follow-Up1: N=54 Follow-Up2: N=54
ITT-Ansatz ohne Imputation; ausgewertet: N=59
Land: Neuseeland 2014-2015 |
Kopf- und NackenkrebspatientInnen,
Geschlecht: 23,76% weiblich
Alter: nicht berichtet Mittelwert: nicht berichtet |
Arm A: N=31 N=29 N=29 Kurze Selbstregulations-Intervention (brief self-regulatory intervention, BSRI), 3 Sitzungen, je 60min, flexible Sitzungen (je nach Wünschen und Bedarf des/der PatientInnen) + Infobroschüre
Arm B: N=31 N=25 N=25 CAU |
Erhebungszeitpunkte Baseline Follow-Up1 (12 Wochen Post-Baseline) Follow-Up2 (24 Wochen)
Primäre Endpunkte: 1. QoL (FACT-HN) 2. Distress (GHQ-12) Krankheitswahrnehmung (Brief IPQ) |
1. QoL à BSRI versus CAU Follow-Up1: Keine sign. Gruppenunterschiede
Follow-Up2: Sign. Gruppenunterschiede zugunsten von BSRI bzgl. Soziale QoL
2. Distress: à BSRI versus CAU: Follow-Up1: Keine sign. Gruppenunterschiede
Follow-Up2: Keine sign. Gruppenunterschiede |
Keine berichtet |
Oakley Mental Health Research Foundation and the Maurice and Phyllis Paykel Trust
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: unclear
Pilotstudie
Geplante Fallzahl (N=68) nicht erreicht |
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Cheung et al., 2016: A randomized pilot trial of a positive affect skill intervention (lessons in linking affect and coping) for women with metastatic breast cancer |
RCT, prospektiv, offen, monozentrisch, 3 Arme
Randomisiert: N=39 Post-Intervention: N=30 Follow-Up: N=27
kA zu Analyse-methode; kA, wie viele ausgewertet
Land: USA 2011-2014 |
Patientinnen mit metastasiertem Brustkrebs
Geschlecht: 100% weiblich
Alter: 30-73 Mittelwert: 53,35 |
Arm A: NR=14 NP=10 NFU1=9 Positive affect skills intervention (Lessons in linking affect and coping, LILAC),5 Wochen, wöchentlich, 5x1h Sitzungen, face-to-face
Arm B: NR=12 NP=9 NFU1=9 LILAC, dieselben Inhalte, nur online und self-paced (also eigenständig durchgeführt), wöchentliche Sitzungen und Hausaufgaben
Arm C: NR=13 NP=11 NFU=9 AC, 5 wöchentliche Sitzungen à 1h, Interviews aber ohne bestimmtes Ziel oder Skilltraining, Hausaufgaben waren tägliche Emotions-Reporte
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Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (4 Wochen)
Primäre Endpunkte: 1. Depressivität (CES-D) 2. Positive und negative Emotionen (DES) 3. QoL (MQOLS-CA) 4. Achtsamkeit (12 Items von 4 verschiedenen Mindfulness-Skalen) 5. Self-Compassion (SCSF) |
1. Depressivität: à LILAC versus AC: Post-Intervention: Keine sign. Gruppenunterschiede
Follow-Up: Keine sign. Gruppenunterschiede; aber sign. within-Veränderung von Baseline zu FU nur in LILAC (d=-.81)
2. QoL à LILAC versus AC: Post-Intervention: Keine sign. Gruppenunterschiede
Follow-Up: Keine sign. Gruppenunterschiede |
Nicht berichtet |
Keine Angaben zur Finanzierung
Laut Angaben keine COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: high RB: unclear
Arm A und Arm B wurden bei Ergebnissen als eine Gruppe behandelt, da sich keine Unterschiede zwischen online vs. Face-to-face zeigten
Pilotstudie
Keine Fallzahlplanung |
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Singer et al., 2017: Effects of stepped psychooncological care on referral to psychosocial services and emotional well‐being in cancer patients: A cluster‐randomized phase III trial |
RCT, prospektiv, offen, multizentrisch, 2 Arme
Randomisiert: N=1012 Post-Intervention: N=1012 Follow-Up1: N=kA Follow-Up2: N=583
Kein ITT-Ansatz; ausgewertet: N=575
Land: Deutschland 2012-2015 |
KrebspatientInnen (am häufigsten Hals- und Nacken, urogenital, Brust, Prostata, Lunge, Leber, gynäkologisch; aber sehr verschiedene Krebsarten in den Gruppen), Stage I-IV
Geschlecht: ca. 40% weiblich
Alter: 19-91 Mittelwert: ca. 63,5 |
Arm A: NR=570 NP=570 NFU1=kA NFU2=341 Stepped care, Screening nach Belastungen (Distress), nach Bedarf psychosoziale Beratung
Arm B: NR=442 NP=442 NFU1=kA NFU2=234 CAU |
Erhebungszeitpunkte Baseline Post-Intervention (Entlassung vom Krankenhaus) Follow-Up1 (12 Wochen Post-Baseline; nicht von Post-Intervention aus gerechnet, da individueller stepped care Ansatz) Follow-Up2 (24 Wochen Post-Baseline)
Primäre Endpunkte: 1. Distress (HADS)
Sekundäre Endpunkte: 1. Inanspruchnahm von weiterer psychosozialer Betreuung (GHS) |
1. Distress: à SC versus CAU: Follow-Up2: Keine sign. Gruppenunterschiede |
Nicht berichtet |
German Federal Ministry of Health within the framework “Research Within the German National Cancer Plan”
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: high
Randomisierung auf Ebene von Stationen, nicht Patient*innen;
Patient*innen mit höheren HADS-Score sign. öfter aus Studie ausgeschieden
Hohe Attritionsrate; vor allem wegen vielen Todesfällen
Geplante Fallzahl (N=800) nicht erreicht |
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Gruppenpsychotherapie RCTs (2015 – 2020)
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Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Patienten-merkmale |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Finanzierung / Conflict of Interest |
Methodische Bemerkungen |
Evidenzklasse |
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Unterstützende Evidenz (12/18) |
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Fernandez-Rodriguez et al. 2020: Behavioral Activation and Acceptance and Commitment Therapy in the Treatment of Anxiety and Depression in Cancer Survivors: A Randomized Clinical Trial |
RCT; prospektiv, monozentrisch, offen, 3 Arme
Randomisiert: N=66 ITT-Ansatz Ausgewertet: N=66 (PP-Analyse Ausgewertet: N=46)
Land: Spanien 2016-2018
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Krebsüberlebende (87% Brust, 4,3% Lunge, Rest anderes) mit Depressionen oder Angststörung (Score über 8 auf einer der Subskalen des HADS); momentan krebs- und behandlungsfrei
Geschlecht: 93,5% weiblich
Alter: Mittelwert: 51,49 |
Arm A: NB=22 NP=17 NFU=17 Verhaltensaktivierung (VA), 12 wöchentliche Sitzungen à 90min, max. 6 PatientInnen pro Gruppe
Arm B: NB=17 NP=12 NFU=12 ACT, 12 wöchentliche Gruppensitzungen à 90 min, max. 6 PatientInnen pro Gruppe
Arm C: NB=27 NP=23 NFU=17 WL |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (3 Monate)
Primäre Endpunkte: 1. Depressivität (HADS-D, BDI-IA-SCA) 2. Angst (HADS-A) 3. Distress (HADS) 4. Verstärkung durch die Umwelt (Environmental Reward Observation Scale (EROS)) 5. Vermeidung und psychische Inflexibilität (AAQ-II) 6. Verhaltensaktivierung (BADS) |
1. Depressivität (HADS-D): à VA versus ACT versus WL Sign. ZeitxGruppe-Interaktion
Kontraste: Post-Intervention: Sign. Gruppenunterschiede zugunsten von VA und ACT, keine Unterschiede zwischen ACT und VA
Follow-Up: Sign. Gruppenunterschiede zugunsten von VA und ACT, keine Unterschiede zwischen ACT und VA
2. Depressivität (BDI-IA-SCA) à VA versus ACT versus WL: Sign. ZeitxGruppe-Interaktion
Kontraste: Post-Intervention: Sign. Gruppenunterschiede zugunsten von VA und ACT, keine Unterschiede zwischen ACT und VA
Follow-Up: Sign. Gruppenunterschiede zugunsten von VA und ACT, keine Unterschiede zwischen ACT und VA
3. Angst: à VA versus ACT versus WL: Sign. ZeitxGruppe-Interaktion
Kontraste: Post-Intervention: Sign. Gruppenunterschiede zugunsten von VA und ACT, keine Unterschiede zwischen ACT und VA
Follow-Up: Sign. Gruppenunterschiede zugunsten von VA und ACT, keine Unterschiede zwischen ACT und VA
4. Distress à VA versus ACT versus WL: Sign. ZeitxGruppe-Interaktion
Kontraste: Post-Intervention: Sign.Gruppenunterschiede zugunsten von VA und ACT, keine Unterschiede zwischen ACT und VA
Follow-Up: Sign. Gruppenunterschiede zugunsten von Va und ACT, keine Unterschiede zwischen ACT und VA
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Keine berichtet |
Laut Angaben keine Finanzierung und keine COI |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Keine Fallzahlplanung (kA).
Berichtete Ergebnisse beziehen sich auf ITT-Analyse, PP-Analyse kommt zu vergleichbaren Ergebnissen |
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Emafti (2019): The Effect of Group Logotherapy on Spirituality and Death Anxiety of Patients with Cancer: An Open-Label Randomized Clinical Trial. |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 64
kA. Ausgewertet: N = 59
Land: Iran 2017
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Krebs-patienten während der Chemo-therapie
Geschlecht: 66.1% weiblich
Alter: 27-68 M = 46.78 |
Arm A: EG NB = 32 NP = 24 (analysiert: N = 29) Logotherapie Gruppe 10 Sitzungen à 2 h über 5 Wochen
Arm B: KG NB = 32 NP = 30 (analysiert: N = 30) CAU
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Erhebungszeitpunkte: Baseline Post-Intervention
Primäre Endpunkte: 1. Todesangst (DAS)
Sekundäre Endpunkte: 1. Spiritualität (SQ) |
1. Todesangst àEG vs. CAU Post Intervention: Sign. Reduktion der Todesangst zugunsten der EG
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Arm A: EG UEs: kA
Arm B: CAU |
Golestan and Mazandaran Universities of Medical Sciences
Laut Angaben kein COI
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Risk of Bias
SB1: low SB2: high PB: high DB: high AB: high RB: low
Geplante Fallzahl (N = 30 pro Gruppe) erreicht. |
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Mani et al. (2019): The effectiveness of group aceptance and commitment psychotherapy on psychological well-being of breast cancer patients in Shiraz, Iran |
RCT prospektiv, monozentrisch, halb-blind, 2 Arme
Randomisiert: N = 30
kA zu ITT-Verfahren (keine Dropouts) Ausgewertet: N = 30
Land: Iran 2014-2016 |
Brustkrebspatienten
Geschlecht: 100% weiblich
Alter: Mittelwert: EG: 44.38 KG: 41.46 |
Arm A: NB = 15 NP = 15 AC, 8 Sitzungen à 2h, verteilt über 4 Wochen
Arm B: N = 15 AC, 8 Nicht-therapeutische Gruppensitzungen (Placebo) |
Erhebungszeitpunkt: Baseline Post-Intervention
Primäre Endpunkte: 1. Pos./neg. Affektivität (PANAS) 2. Hoffnung (AHS) 3. QoL |
1. QoL à ACT vs. AC Post-Intervention: Sign. Gruppenunterschied zugunsten von ACT (d = 0.72).
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Keine berichtet. |
Finanzierung durch Vize Forschungskanzler der Shiraz University of Medical Sciences
Laut Angabe kein COI. |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N = 30) erreicht. |
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Peng et al. (2019): Responses of lung cancer survivors undergoing gamma knife surgery to supportive group psychotherapy |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 160
PP-Analyse Ausgewertet: Baseline: N = 160
Post-Intervention: N = 155
3-Monate-Follow-Up: N = 150
Land: China 2017-2018
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Lungenkrebspatienten, Stage III & IV, Gamma Knife Radiochirurgie (GKS)
Geschlecht: EG: 48.8% weiblich, KG: 44.9% weiblich
Alter: Mittelwert: EG: 61.4 KG: 59.4
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Arm A: NB = 82 NP = 80 NFU = 78 Unterstützende Gruppenpsychotherapie (SGP): 8 Wochen, 1x/Woche, 90 Min.
Arm B: NB = 78 NP = 75 NFU = 72 TAU |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (3 Monate)
Primäre Endpunkte: 1. Depressivität (HADS-D) 2. Angst (HADS-A)
Sekundärer Endpunkt: 3. QoL, krebsbezogen (EORTC QLQ-C30) |
1. Depressivität à SGP vs. TAU Post-Intervention und Follow-Up: Sign. Gruppenunterschiede zugunsten der SGP.
2. Angst à SGP vs. TAU Post-Intervention und Follow-Up: Sign. Gruppenunterschiede zugunsten der SGP.
3. QoL, krebsbezogen à SGP vs. TAU Post-Intervention und Follow-Up: Sign. Gruppenunterschiede auf allen funktionellen Skalen zugunsten der SGP
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Keine berichtet. |
Laut Angabe kein COI. |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: unclear RB: unclear
Keine Fallzahlplanung (kA) |
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Ren et al. (2019): Randomized controlled trial of cognitive behavioural therapy for depressive and anxiety symptoms in Chinese women with breast cancer |
RCT, prospektiv, multizentrisch, offen, 3 Arme
Randomisiert: N = 392
ITT-Ansatz Ausgewertet: N = 392
Land: China Zeitraum: kA
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Brustkrebspatientinnen, Angst- und/oder Depressionssymptome
Geschlecht: 100% weiblich
Alter: Mittelwert: KVT: 46.8 SCM: 47.3 UC: 47.1 |
Arm A: NB = 98 NFU = 91 KVT: 12 Wochen, 9 Sitzungen, 6-8 TN
Arm B: NB = 98 NFU = 90 Selbstfürsorge/Selbstmanagement (SCM): 12 Wochen. 9 Sitzungen, 6-8 TN
Arm C: NB = 196 NFU = 175 CAU |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (8 Wochen)
Primäre Endpunkte: 1. Depressivität (HAMD-17) 2. Angst (HAMA-14) |
1. Depressivität à KVT vs. SCM vs. CAU Sign. Zeit x Gruppe-Interaktion (ηp² = 0.141).
Sign. Gruppenunterschied über alle Zeitpunkte zugunsten der KVT > SCM > CAU (ηp² = 0.201)
Sign. Effekt der Zeit bei allen Gruppen (ηp² = 0.701), aber KVT > SCM > CAU
Post-Intervention: HAMD-Werte in KVT-Gruppe unter Cut-Off.
2. Angst à KVT vs. SCM vs. CAU Sign. Zeit x Gruppe-Interaktion (ηp² = 0.092).
Sign. Gruppenunterschied über alle Zeitpunkte zugunsten der KVT > SCM > CAU (ηp² = 0.173)
Sign. Effekt der Zeit bei allen Gruppen (ηp² = 0.701), aber KVT > SCM > CAU
Post-Intervention: HAMA-Werte in KVT-Gruppe unter Cut-Off.
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Keine berichtet. |
Finanzierung durch National Key Technologies R&D Programm, 11. 5-Jahresplan des Ministeriums für Wissenschaft und Technik der Volksrepublik China. Kein weiterer Einfluss der Geldgeber auf Studienplanung, -durchführung und Auswertung.
Laut Angabe kein COI. |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: high
Post-hoc Power Analyse: “Power analyses based on the sample size showed that the study retained 90% power to identify the effect sizes, with an α of 0.05.” |
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Tomei et al. (2018). Examining the preliminary efficacy of an intervention for fear of cancer recurrence in female cancer survivors: a randomized controlled clinical trial pilot study |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 25
kA zu ITT-Verfahren Ausgewertet: N = 24
Land: Kanada Zeitraum: kA |
Krebspatientinnen (Brustkrebs, gynäkologische und okuläre Melanome)
Geschlecht: 100% weiblich
Alter: 34-74 Mittelwert: 55 |
Arm A: N=11 Rezidivangst-(Fear of Cancer Recurrence (FCR)) Intervention, 6 Wochen, wöchentliche Sitzungen à 60-90min
Arm B: N = 14 WL |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (3 Monate)
Primärer Endpunkt: 1. Rezidivangst (FCRI)
Sekundäre Endpunkte: 2. Distress (IES) 3. QoL (SF-8) 4. Unsicherheit (MUIS-C) 5. Wahrgenommene Vorteile des sich Sorgens (WW-H, IUS) Coping (CAQ, RQ; Brief COPE-Q)) |
1. Rezidivangst à EG vs. WL Sign. Gruppe x Zeit-Interaktion
Sign. Verbesserungen zu Post und FU für EG, nicht für KG
2. Distress à EG vs. WL Sign. Gruppe x Zeit-Interaktion
3. QoL à EG vs. WL Keine sign. Gruppe x Zeit-Interaktion |
Keine berichtet. |
Laut Angabe kein COI. |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: high
Pilot-Studie
Geplante Fallzahl (N = 14 pro Gruppe) nicht erreicht. |
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Pettiford et al. (2017): A bio-psychosocial intervention program for improving quality of life in breast cancer survivors – final outcome of a prospective randomized trial |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 120 (N = 60 pro Gruppe)
PP-Analyse Ausgewertet: N = 103
Land: USA Zeitraum: kA
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Brustkrebspatienten
Geschlecht: 100% weiblich
Alter: Mittelwert: EG: 59.7 KG: 60.0
|
Arm A: N = 47 Biopsychosoziale Intervention (BPSI): Mind. 1 Gruppensitzung & optionale Follow-Up-Einzelsitzung
Arm B: N = 56 TAU (standard of cancer and follow-up care, SOC) |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up1 (6 Monate) Follow-Up2 (12 Monate) Follow-Up3 (18 Monate)
Primärer Endpunkt: 1. QoL (FACT-B Gesamtscore) |
1. QoL à BPSI vs. TAU Post-Intervention: Kein sign. Gruppenunterschied.
Follow-Up1: Sign. Gruppenunterschied zugunsten von BPSI.
Follow-Up2: Sign. Gruppenunterschied zugunsten von BPSI.
Follow-Up 3: Kein sign. Gruppenunterschied.
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Keine berichtet. |
Laut Angabe kein COI. |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: unclear RB: unclear
Geplante Fallzahl (N = 60 pro Gruppe) nicht erreicht. |
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Van der Spek et al. (2017): Efficacy of meaning-centered group psychotherapy for cancer survivors: a randomized controlled trial |
RCT, prospektiv, multizentrisch, offen, 3 Arme
Randomisiert: N = 170
ITT-Ansatz Ausgewertet: N = 170
Land: Niederlande 2012-2014 |
Krebsüberlebende, diagnostiziert in den letzten 5 Jahren, abgeschlossene Therapie
Geschlecht: MCGP-CS: 70% weiblich SGP: 88% weiblich CAU: 90% weiblich
Alter: Mittelwert: MCGP-CS: 58.6 SGP: 55.5 CAU: 10.4 |
Arm A: NB = 57 NP = 50 NFU1 = 48 NFU2 = 45 Sinnbasierte Gruppenpsychotherapie für Krebsüberlebende (MCGP-CS): 8 Wochen, 1x/Woche, 2h
Arm B: NB = 56 NP = 49 NFU1 = 48 NFU2 = 46 Sozial-unterstützende Gruppentherapie (SGP): 8 Wochen, 1x/Woche, 2h
Arm C: N = 57 NP = 47 NFU1 = 40 NFU2 = 35 CAU |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up1 (12 Wochen) Follow-Up2 (24 Wochen)
Primärer Endpunkt: 1. Persönliche Bedeutung (personal meaning, PMP-DV)
Sekundäre Endpunkte: 2. Psychisches Wohlbefinden (SPWG: 8 Subscalen) 3. Posttraumatisches Wachstum (PTGI) 4. Mentale Anpassung an Krebs (MAC, 5 Subscalen) 5. Optimismus (LOT-R) 6. Hoffnungslosigkeit (BHS) 7. Distress (HADS Geamtscore, Angst: HADS-A, Depressivität: HADS-D) 8. QoL global (EORTC QLQ-C30)
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1. Psychische Belastung à MCGP-CS vs. CAU
Follow-Up1: Sign. Gruppenunterschiede für psychische Belastung und Depressivität zugunsten der MCGP-CS (d = -0.6 bzw. d = -0.38). Keine sign. Gruppenunterschiede hinsichtlich Angst.
Zu Post-I. und Follow-Up2 keine sign. Gruppenunterschiede
2. QoL è MCGP-CS vs. CAU Post-Intervention & Follow-Up1 bzw. 2: Keine sign. Gruppenunterschiede.
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Keine berichtet |
Laut Angabe kein COI. |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: high
Geplante Fallzahl (N = 56 pro Gruppe zu Baseline) erreicht. |
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Dowlatabadi (2016): The effectiveness of group positive psychotherapy on depression and happiness in breast cancer patients: A randomized controlled trial. |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 42
PP-Analyse Ausgewertet: N = 33
Land: Iran 2013-2015
|
Brustkrebs-patientinnen
Geschlecht: 100% weiblich
Alter: 24-32: 30.3% 33-41: 54.5% 42-50: 15.2%
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Arm A: IG NB = 21 NP = 16 Positivistische Gruppen-psychotherapie (PGT) 10 x 1,5 h, wöchentliche Sitzungen
Arm B: KG NB = 21 NP = 17 Keine Intervention |
Erhebungszeitpunkte: Baseline Post-Intervention
Primäre Endpunkte: 1. Depressivität (BDI-II) 2. Glückselig-keit (OHI)
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1. Depressivität à PGT vs KG Post Intervention: Sign. Reduktion der Depressivität zugunsten der PGT
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Arm A: IG UEs: kA
Arm B: KG |
Kermanshah University of Medical Sciences (Iran)
Laut Angaben kein COI |
Risk of Bias
SB1:unclear SB2: unclear PB: high DB: high AB: low RB: high
Keine Fallzahlplanung (kA). |
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Mohabbat-Bahar et al. (2015): Effectiveness of group training based on acceptance and commitment therapy on anxiety and depression of women with breast cancer |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 30
kA zu ITT-Verfahren (keine Dropouts) Ausgewertet: N = 30
Land: Iran Zeitraum: kA
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Brustkrebspatienten Stage I-III, abgeschlossene Therapie
Geschlecht: 100% weiblich
Alter: EG: 44-59, Mittelwert: 49.66
KG: 29-59 Mittelwert: 45.4
|
Arm A: N = 15 ACT, 8 Gruppen- therapiesitzungen à 90 Min., verteilt über 4 Wochen
Arm B: N = 15 TAU |
Primäre Endpunkte: 1. Angst (BAI) 2. Depressivität (BDI-II) |
1. Angst à ACT vs. TAU Post-Intervention: Sign. Gruppenunterschied zugunsten der ACT (η = 0.545)
2. Depressivität à ACT vs. TAU Post-Intervention: Sign. Gruppenunterschied zugunsten der ACT (η = 0.616) |
Keine berichtet. |
Laut Angabe kein COI. |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: low RB: unclear
Keine Fallzahlplanung (kA). |
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Stagl et al. (2015). Long-term psychological benefits of cognitive-behavioral stress management for women with breast cancer_ 11-year follow-up of a randomized controlled trial |
RCT, prospektiv, monozentrisch, einfach verblindet, 2 Arme
Randomisiert: N = 240
PP-Ansatz Ausgewertet: N = 100 (CBSM: N = 49, KG: N = 51)
Land: USA 1998-2005 (Follow-Up: 2013) |
Nicht metastatischer Brustkrebs, Stage 0-IIIb, 2-10 Wochen Post-OP
Geschlecht: 100% weiblich
Alter: Mittelwert (Follow-Up): 62.47 |
Arm A: NB = 120 NP = 96 NFU1 = 95 NFU2 = 60 NFU3 = 49 Kognitiv-behaviourales Stressmanagment (CBSM): 10 Wochen, 1x/Woche, 90 Min.
Arm B: NB = 120 NP = 98 NFU1 = 96 NFU2 = 70 NFU3 = 51 AC, Psychoedukatives “Selbsthilfe” Seminar (1 Tag)
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Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up1 (6 Monate) Follow-Up2 (4,5 Jahre) Follow-Up3 (8-15 Jahre Jahre)
Primäre Endpunkte: 1. Depressivität (CES-D) 2. QoL, (FACT-B) |
1. Depressivität à CBSM vs. AC Follow-Up 3: Sign. Gruppenunterschiede zugunsten des CBSM
2. QoL à CBSM vs. AC Follow-Up 3: Sign. Gruppenunterschiede zugunsten des CBSM
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Keine berichtet. |
Finanzierung durch National Cancer Institute oft he National Institutes of Health.
M. H. Antoni: erhält Lizenzgebühren für Veröffentlichung und dazugehörige Materialien
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Risk of Bias
SB1: unclear SB2: unclear PB: high DB: low AB: low RB: unclear
Keine a priori Fallzahlplanung (kA).
" The current sample size was sufficient to detect an effect of medium magnitude with 95% power". |
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Weisflog et al. (2015): Does psychodynamic short-term psychotherapy for depressed breast cancer patients also improve fatigue? Results from a randomized controlled trial |
RCT, prospektiv, multizentrisch, offen, 2 Arme
Randomisiert: N = 157
PP-Ansatz Ausgewertet: N = 106
Land: Deutschland Zeitraum: kA
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Brustkrebspatientinnen, HADS-D Score über oder gleich Cut-Off (HADS C 8) bzw. mind. 1 depressive Störung
Geschlecht: 100% weiblich
Alter: Mittelwert: EG: 52.6 KG: 52.3 |
Arm A: NB = 78 NP = 52 Psychodynamische Kurzzeittherapie (STPP)
Arm B: NB = 79 NP = 54 TAU |
Erhebungszeitpunkte: Baseline Post-Intervention
Primärer Endpunkt: 1. Fatigue (MFI-20)
Sekundäre Endpunkte: 2. QoL global (EORTIC QLQ-30) 3. Depressivität (SCID-I, HADS-D)
à sekundäre Endpunkte in Beutel et al. 2014 berichtet und daher nicht mit aufgenommen |
1. Fatigue à STPP vs. TAU Sign. Zeit x Gruppe-Interaktion für Gesamtscore zugunsten von STPP
Post-Intervention: Abnahme der Fatigue-Werte beider Gruppen
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Keine berichtet. |
Laut Angabe kein COI. |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: high RB: high
Keine Fallzahlplanung (kA) |
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Conley & Andersen (2019): Lemons to Lemonade: Effects of a Biobehavioral Intervention for Cancer |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 227
PP-Analyse Ausgewertet: 12 Monate: N = 201 24 Monate: N = 160
Land: USA kA zum Zeitraum |
Brustkrebs-patientinnen (Stadien II oder III)
Geschlecht: 100% weiblich
Alter: M = 51
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Arm A: BBI (biobehavioral intervention) NB = 114 NP = 106 NFU = 85 Psychosoziale Gruppen-intervention (Stress, QoL, Gesundheits-verhalten) 18 x 1,5h, wöchentliche Sitzungen + 8 monatliche Sitzungen, Insgesamt 12 Monate
Arm B: KG NB = 113 NP = 95 NFU = 75 Keine Intervention
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Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (12 Monate)
Primäre Endpunkte: 1. Gedanken über Veränderung
Sekundäre Endpunkte: 2. Distress (IES) 3. Depressivität (CES-D) |
1. Distress à BBI vs. KG Follow-Up: Keine sign. Gruppenunterschiede
2. Depressivität à BBI vs. KG Follow-Up: Keine sign. Gruppenunterschiede |
Arm A: BBI UEs: kA
Arm B: KG |
National Cancer Institute (USA) + National Institute of Mental Health (USA) + American Cancer Society + U.S. Army Medical Research Acquisition Activity Breast Cancer Research Program + Walther Cancer Institute
Laut Angaben kein COI |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: unclear RB: unclear
Geplante Fallzahl (N = 200) zu Baseline & Post-Intervention erreicht. |
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Esplen (2018): Restoring Body Image After Cancer (ReBIC): Results of a Randomized Controlled Trial. |
RCT prospektiv, multizentrisch, offen, 2 Arme
Randomisiert: N = 194
ITT-Analyse Ausgewertet : N=194
Land: Kanada kA zum Zeitraum |
Brustkrebs-Überlebende, abgeschlossene Krebsbehandlung seit min. 2 Jahren, Stage I-III
Geschlecht: 100% weiblich
Alter: Mittelwert: 49,8 |
Arm A: NB=131 NP=111 NFU1=108 NFU2=104 Restoring body image after cancer (ReBIC), 8-wöchige 90min Gruppenintervention, wöchentliche Sessions, beinhaltete expressive guided-imagery Übungen sowie Gruppentherapieprinzipien
Arm B: NB=63 NP=54 NFU1=108 NFU=53 CAU + schriftliche edukative Infos
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Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up1 (4 Monate) Follow-Up2 (10 Monate)
Primäre Endpunkte: 1. Körperbild (BIS, BIBCQ) 2. Sexuelle Funktion (FSFI) 3. QoL global (FACT-B) |
1. Sexuelle Funktion: à ReBIC versus CAU: Post-Intervention: Follow-Up1: Follow-Up2: Keine sign. ZeitxGruppe-Interaktion, keine sign. Gruppenunterschiede
2. QoL à ReBIC versus CAU: Post-Intervention: Follow-Up1: Follow-Up2: Keine sign. ZeitxGruppe-Interaktion, keine sign. Gruppenunterschiede
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Keine berichtet |
Canadian Breast Cancer Research Alliance and a grant from the Canadian Breast Cancer Foundation
Laut Angaben keine COI
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Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Keine Fallzahlplanung (kA). |
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Ho et al. (2016): Randomized controlled trial of supportive-expressive group therapy and body-mind-spirit interventions for Chinese non-metastatic breast cancer patients |
RCT prospektiv, multizentrisch, offen, 3 Arme
Randomisiert: N = 157
ITT-Ansatz Ausgewertet: N = 157
Land: Hong Kong (China) 2002-2004 |
Nicht-metastatische Brustkrebspatienten Stage: I-III, Abgeschlossene Behandlung
Geschlecht: 100% weiblich
Alter: Mittelwert: 47.7 |
Arm A: NB = 51 NP = 50 NFU1 = 49 NFU2 = 48 Body-Mind-Spirit-Therapie (BMS): 8 Wochen 2h/Woche 8-12 TN/Gruppe
Arm B: NB = 49 NP = 47 NFU1 = 47 NFU2 = 44 Supportive-Expressive Therapie (SEG) 8 Wochen 2h/Woche 8-12 TN/Gruppe
Arm C: NB = 57 NP = 51 NFU1 = 48 NFU2 = 47 TAU |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up1 (7 Monate) Follow-Up2 (11 Monate)
Primäre Endpunkte: 1. Emotionsunterdrückung (CECS) 2. Stresserleben (PSS, chinesische Version) 3. Angst (C-HADS-A) 4. Depressivität (C-HADS-D) |
1. Angst à BMS vs. SEG vs. TAU Post-Intervention, Follow-Up1 & 2: Keine sign. Veränderung in jeglicher Gruppe. Keine sign. Gruppenunterschiede.
2. Depressivität à BMS vs. SEG vs. TAU Post-Intervention, Follow-Up1 & 2: Keine sign. Veränderung in jeglicher Gruppe. Keine sign. Gruppenunterschiede.
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Keine berichtet. |
Finanzierung durch Hong Kong Cancer Fund und Hong Kong Research Grants Council. Laut Angabe keinen Einfluss auf Studiendesign, Datenerhebung, Analyse, Berichterstellung, Entscheidung für Veröffentlichung.
Laut Angabe kein COI. |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N = 150) erreicht. |
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Naccarato et al. (2016): Psychotherapy and phosphodiesterase-5 inhibitor in early rehabilitation after radical prostectomy: a prospective randomised controlled trial |
RCT, prospektiv, monozentrisch, offen, 4 Arme
Randomisiert: N = 56
PP-Analyse Ausgewertet: N = 53
Land: Brasilien
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Prostatakrebspatienten mit radikaler Prostatektomie (RP), frühes Rehabilitationsstadium
Geschlecht: 100% männlich
Alter: 39-76 Mittelwert: 61.84 |
Arm A: N = 16 Gruppen-PT Wöchentlich, 2 Sitzungen vor RP, 12 nach RP
Arm B: N = 12 Medikation (M): Lodafenil 80 mg/1 Tablette pro Woche
Arm C: N = 14 Gruppen-PT & Medikation
Arm D: N = 11 TAU
|
Erhebungszeitpunkte: Baseline Post-Intervention
Primäre Endpunkte: 1. Sexuelle Funktion (IIEF-5) 2. QoL (SF-36) |
1. Sexuelle Funktion à TAU vs. PT vs. M vs. PT & M Post-Intervention: Nur PT & M zeigt keine sign. Verschlechterung des IIEF-5
2. QoL à TAU vs. PT vs. M vs. PT & M Post-Intervention: Sign. Verschlechterung d. Skalen phys. Gesundheit & Rollenfunktion aller Gruppen
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Arm A: TAU SUEs: 0/11 UEs: 0/11
Arm B: PT SUEs: 0/16 UEs: 0/16
Arm B: Medikation SUEs: 0/12 UEs: 0/12 (keine sign. S/UEs)
Arm D: PT & Medikation SUEs: 0/14 UEs: 0/14 |
kA |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: unclear RB: unclear
Geplante Fallzahl (N = 11 pro Gruppe) erreicht. |
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Schneider et al. (2016): Ergebnisse einer psychoonkologischen Gruppenintervention bei männlichen Krebspatienten ab 60 Jahre - eine randomisiert kontrollierte Studie |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 51 Post-Intervention: N=45 Follow-Up: N=38
kA zur Auswertungs-Strategie
Land: Deutschland Zeitraum: 10/2012 – 08/2014
|
Prostatakarzinom oder gastrointestinales Malignom aller Krankheitsstadien
Geschlecht: 100% männlich
Alter: Mittelwert: 67.2 |
Arm A: NB = 25 NP = 23 NFU = 20 Psychosoziale Gruppenintervention, 10 Wochen, 1 Sitzung/Woche, 120 Min., 6-10 TN
Arm B: NB = 26 NP = 22 NFU = 18 TAU |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (3 Monate)
Primärer Endpunkt: 1. QoL global (EORTIC QLQ-C30)
Sekundäre Endpunkte: 2. Angst (HADS-A) 3. Depressivität (HADS-D) 4. Zufriedenheit mit dem Gruppenprogramm (Fragebögen aus Manual Weis (2006)) |
1. QoL (global) à Gruppe vs. TAU Post-Intervention: Keine sign. Gruppenunterschiede
Follow-Up: Keine sign. Gruppenunterschiede
2. Depressivität à Gruppe vs. TAU Post-Intervention: Keine sign. Gruppenunterschiede
Follow-Up: Keine sign. Gruppenunterschiede
3. Angst à Gruppe vs. TAU Post-Intervention: Keine sign. Gruppenunterschiede
Follow-Up: Sign. höhere Angstwerte in Gruppe!
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Sign. Verschlechterung der Interventionsgruppe ggü. TAU auf Schlafstörungsskala sowie emotionaler Funktionsfähigkeit |
KA |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: unclear RB: unclear
Keine Fallzahlplanung (kA)
Keine Angabe von Drop-Out-Gründen |
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Freeman et al., 2015: A randomized trial comparing live and telemedicine deliveries of an imagery-based behavioral intervention for breast cancer survivors: reducing symptoms and barriers to care |
RCT prospektiv, multizentrisch, offen, 3 Arme
Randomisiert: N = 118
ITT-Ansatz Ausgewertet: N = 118
Land: USA 2008-2010 |
Brustkrebs-Überlebende, mindestens 6 Wochen nach abgeschlossener Behandlung
Geschlecht: 100% weiblich
Alter: Mittelwert: 55.44
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Imaginationsbasierte Verhaltensintervention (Arm A & B): 1x/Woche à 4h, 1.-4. Sitzung: 25 Min. Theorie, 25 Min. Interaktion in Triaden 5. Sitzung: Präsentation ind. Beiträge & Feedback
Arm A: NB = 48 NP = 41 NFU = 40 Gruppenangebot Edukation+Imagination+Übungen (Life Delivery, LD), 50min (25min Input, 25min Interaktion), wöchentlich, 5 Wochen + Übungen zuhause
Arm B: NB = 23 NP = 19 NFU = 19 Wie oben, nur: Online-Gruppe, Telemedizin (telemedecine delivery, TD)
Arm C: NB = 47 NP = 44 NFU = 43
WL, Angebot der ERL-Intervention nach 3-Monats-Follow-Up
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Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (2 Monate)
Primärer Endpunkt: 1. Allg. QoL (SF-36): physisch (PCS), psychisch (MCS)
Sekundäre Endpunkte: 2. Krebsbezogene QoL (FACT-B) 3. Fatigue (FACIT-F) 4. Wahrgen. kogn. Funktionsfähigkeit (FACT-Cog) 5. Spirituelles Wohlbefinden (FACIT-Sp-Ex) 6. Distress (BSI-GSI) 7. Schlafstörungen (PSQI) |
1. Allg. QoL (psychisch) à LD vs. TD vs. WL: Keine sign. Effekte für Zeit, Gruppe, Zeit x Gruppe-Interaktion.
2. Krebsbezogene QoL à LD vs. TD vs. WL: Sign. Effekt für Zeit.
3. Fatigue à LD vs. TD vs. WL: Sign. Effekt für Gruppe. Keine sign. Effekte für Zeit, Zeit x Gruppe-Interaktion.
4. Distress à LD vs. TD vs. WL: Keine sign. Effekte für Zeit, Gruppe, Zeit x Gruppe-Interaktion.
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Keine berichtet. |
Finanzierung durch Small Business Innovating Research-Subvention + Krebspräventions-Stipendium für Mitarbeitende (NCI grant)
Laut Angaben kein COI. |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Keine Fallzahlplanung |
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Entspannungsverfahren und imaginative Verfahren
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Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Merkmale untersuchter Studien |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Methodische Bemerkungen |
Evidenzklasse |
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Hilfiker et al. 2018: "Exercise and other non-pharmaceutical interventions for cancer-related fatigue in patients during or after cancer treatment: a systematic review incorporating an indirect-comparisons meta-analysis."
Eingeschlossene Primärstudien: 245 Primärstudien |
Indirect-comparison MA
Suchzeitraum: Januar 2017
Datenbanken: Pubmed CENTRAL
Einschluss-kriterien: P: erwachsene Krebspatienten I: Bewegungs- oder nicht-pharmakologische Therapie C: TAU/UC O: Fatigue S: RCTs
112 RCTs in MA Intervention während laufender Krebsbehandlung
133 RCTs in MA Interventionen nach abgeschlossener Krebsbehandlung
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RCTs
Brustkrebs (126) Hämatologischer Krebs (10) Prostatakrebs (18) Kolorektaler Krebs (7) Gemischte Krebsidiagnosen (52)
Geschlecht: >65% weiblich
Mittleres Alter: kA
Länder : Keine zusammenfas-senden Angaben, Details in Appendices
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Inhalte: Während Behandlung Ausdauer (34) Ausdauer + Gewichte (23) CBT (18) Entspannung (12) à inkl. Atmung, Stretching, Meditation Yoga (10) Gewichte (10) Multimodal (6) Massage (4) Heilende Berührung (3) Tanztherapie (2) Musiktherapie (1)
Nach Behandlung Ausdauer (30) Ausdauer + Gewichte (32) CBT (29) Entspannung (kA) à inkl. Atmung, Stretching, Meditation Yoga (kA) Gewichte (kA) Multimodal (kA) Massage (kA) Heilende Berührung (kA) Tanztherapie (kA) Musiktherapie (kA)
Dauer/Frequenz/ Länge: 3-52 Wochen 0-12 Wochen Follow-Up Individual-, Gruppen-, und Paarsetting, Tele- und EHealth
Kontrollgruppen: TAU/UC |
Primäre Endpunkte: 1.Fatigue
Verwendete Messinstrumente: CFS PFS PFS-Revised EORTC QLQ-C30 Fatigue BFI POMS FACIT-F FACT-F etc.
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1. Fatigue Während Behandlung àEntspannung: Post-Intervention: 12 RCTs, I2 = 88%; SMD=–0.77 [–1.22, –0.31, p <.05>
Nach Behandlung àEntspannung: Post-Intervention: ? RCTs, I2 = ? %; SMD=–0.05 [–0.64, 0.53, p <.05>
|
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB "Over all comparisons, the random sequence generation was adequate in most trials (97%); allocation concealment was problematic in 61% of the trials. Baseline characteristics were not balanced in 17% of the studies; patients and outcome assessor could not be blinded in most trials (99%), therapists were never blinded. More than 15% of drop-outs were present in 36% of the trials and only 51% of the trials reported an intention-to-treat analysis. (p.654)
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,11,15 non-kritischer Dom. 1,3,10
Sensitivitäts-analysen: Ausschluss von Studien mit n<25 Teilnehmern pro Arm; Effekte generell kleiner, keine Änderung des Signifikanzniveaus in relev. Effekten; kein Einfluss auf Heterogenität
Publikations-bias: Egger's Test liefert Hinweise Publikations-Bias in relev. Vergleichen |
1a- |
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Sanjida et al. 2018: "Are psychological interventions effective on anxiety in cancer patients? A systematic review and meta-analyses."
Eingeschlossene Primärstudien: 71 Primärstudien in qual. Review / 51 in Meta-Analysen |
SysRev & MA
Suchzeitraum: Januar 1993– Juni 2017
Datenbanken: CENTRAL Medline Embase CINHAL Scopus PsycInfo
Einschluss-kriterien: P: erwachsene Krebspatienten I: psychosoziale Intervention C: alternative Intervention, TAU/UC, Warteliste O: Angst, Distress S: RCTs
71 RCTS, N=13098 Patientinnen
51 RCTs, N=8283 Patientinnen in MA
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RCTs
Brustkrebs (36) Gynäkologische Tumore (3) Prostata- und Hodenkrebs (2) Sonstige Krebsidiagnosen (29)
Geschlecht: 74,6% weiblich
Mittleres Alter: 55
Länder : USA (19) Europa (29) Weitere (53)
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Inhalte: 14 x CBT 12 x Entspannungs-verfahren 9x Psychosoziale Therapie 13x "Supportive Care Interventions" 3x gestufte Interventionen ("stepped care") 20x sonstige
Dauer/Frequenz/ Länge: 4 Tage – ein Jahr
Kontrollgruppen: alternative Intervention TAU/UC Warteliste |
Primäre Endpunkte: 1. Angst
Verwendete Messinstrumente: Angst HADS STAI POMS
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1. Angst àGesamteffekt: Post-Intervention: 51 RCTs, n=7491 I2 = 68%; SMD=–0.21 [–0.30, –0.13, p < .001] à Sensitivitätsanalyse: Entfernung der Studie mit größtem und kleinsten Effekt, keine Änderung des Ergebnis
àEntspannung: Post-Intervention: 12 RCTs, I2 = 78%; SMD=–0.53 [–0.79, –0.26, p < .05] |
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 18 PB: 2 DB: 7 AB: 42 RB: 48 OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 7,11,15 non-kritischer Dom. 5,8
Sensitivitäts-analysen: durchgeführt, siehe Hauptergebnisse
Durchführung von Subgruppen-analysen, teilweise in Hauptergebnissen aufgeführt
Publikations-bias: "Studies with a sample size of less than 40 participants were excluded to reduce the potential influence of publication bias and inflated ES common in small studies." |
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Tian et al. 2020: "Progressive muscle relaxation is effective in preventing and alleviating of chemotherapy-induced nausea and vomiting among cancer patients: a systematic review of six randomized controlled trials."
Eingeschlossene Primärstudien : Arakawa et al. 1995 Arakawa et al. 1997 Li et al. 2019 Luo et al. 2016 Song et al. 2013 Zhang et al. 2017
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SysRev
Suchzeitraum: Bis 30. Mai 2019
Datenbanken: CENTRAL CINHAL CBM CNKI Wanfang data database
Einschluss-kriterien: P: Erwachsene Krebspatienten mit Chemotherapie I: PMR als einzige Intervention C: routine care O: Übelkeit und Erbrechen S: RCTs
6 RCTS, N=358 Patienten |
RCTs
Erwachsene Krebspatienten (Lunge 2, Brust 2, Gemischt 2) vor und während Chemotherapie
Geschlecht: 37,9% weiblich
Mittleres Alter: 43,6 – 57,7
Länder : China, Japan |
PMR (ausschließlich)
Länge & Frequenz: 15-30min pro Sitzung, 1-2x täglich, 3 Tage – 3 Wochen,
Kontrollgruppen: TAU |
Primäre Endpunkte: 1. Übelkeit 2. Erbrechen induziert durch Chemotherapie
Verwendete Messinstrumente: CTCAE MASCC-AT INV-2 MANE RSS |
Signifikant stärkere Reduktion von Übelkeit in IG verglichen mit CG in allen Studien
Signifikant stärkere Reduktion von Erbrechen in IG verglichen mit CG in 5/6 Studien
Keine Effektstärken berichet
Follow-Up-Zeiträume: 3 Tage nach Behandlung – 3 Wochen nach Behandlung
"The results of the present systematic review indicated that several independent studies have reported a significant beneficial effect of PMR training on the chemotherapy-induced nausea and vomiting as measured by relevant tools" (p. 6) |
Keine SUEs berichtet
RCTs berichten UEs nicht |
Primärstudien: RCTs mit hohem (3) und unklarem (3) Biasrisiko SB:1 PB: 3 DB: unclear AB: 0 RB: 0 OB: 2
Review: AMSTAR-2: low quality Method.Mängel in kritischer Domäne 7 non-kritischer Dom. 3,8,14
Publikationsbias: nicht berichtet |
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Kapogiannis et al. 2018 " Investigating the Effects of the Progressive Muscle Relaxation-Guided Imagery Combination on Patients with Cancer Receiving Chemotherapy Treatment: A Systematic Review of Randomized Controlled Trials."
Primärstudien: Walker et al. 1999 Yoo et al. 2005 Eremin et al. 2009 Chen et al. 2015 Charalambous et al. 2016 |
SysRev
Suchzeitraum: Jan 1990 – 21. Okt 2016
Datenbanken: AMED CENTRAL Pubmed Scopus
Einschluss-kriterien: P: Erwachsene Krebspatienten mit Chemotherapie I: PMR mit GI S: RCTs
7 RCTS, N=588 Patienten
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RCTs
Erwachsene Krebspatienten (Brust 6, Brust und Prostata 1) vor und während Chemotherapie; unterschiedliche Erkrankungsstadien
Geschlecht: Keine Angabe
Mittleres Alter: Keine Angabe
Länder : UK, Hong Kong, Südkorea, Taiwan, Zypern |
PMR in Verbindung mit GI
Länge & Frequenz: 4 Studien 30min pro Sitzung, sonst keine Angabe,
1x täglich,
Keine Angaben zur Sitzungsanzahl,
Kontrollgruppen: Keine Angabe |
1. Stimmung 2. Lebensqualität 3. Depressivität 4. Stress 5. Angst 6. Fatigue 7. Übelkeit 8. Erbrechen 9. Biomarker
Eine Studie untersuchte ausschließlich Biomarker Verwendete Messinstrumente: EPQR CECS L-Scale RSCL GQOL MANE STAI POMS MAACL FACT-B HADS SDS EORTC QLQ-C30 BDI-II RINVR ZSRAS CFS |
"Seven of the included trials reported beneficial effects on mental state (mood, anxiety, and depression) and on toxicity (nausea and vomiting)." (p.137)
Nur narrative Ergebnisdarstellung, Keine Effektstärken berichet
Follow-Up-Zeiträume: 6 Tage bis 6 Monate nach Ende der Chemotherapie
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Keine SUEs berichtet
RCTs berichten UEs nicht |
Primärstudien: Jadad-Scores 2x0/5, 2x2/5, 3x3/5 SB: unclear PB: unclear DB: unclear AB: 0 RB: unclear OB: unclear
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7 non-kritischer Dom. 1,3,5,8,10,16
Publikationsbias: nicht berichtet |
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Faller et al. 2013: "Effects of Psycho-Oncologic Interventions on Emotional Distress and Quality of Life in Adult Patients with Cancer: Systematic Review und Meta-Analysis."
Eingeschlossene Primärstudien: 198 RCTs
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MA
Suchzeitraum: May 2013
Datenbanken: CENTRAL Medline PsycInfo
Einschluss-kriterien: P: erwachsene Krebspatienten I: psychoonkologische Interventionen C: Aufmerkamkeits-Placebo, TAU/UC O: Distress, QoL, Depressivität, Angst S: RCTs
198 RCTS, N=22238 Patientinnen (218 Vergleiche in MA)
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RCTs
Gemischte Krebsdiagnosen (80) Brustkrebs (78) Prostatakarz. (8) Gynekologisch (6) Melanom (5) Hematologischer Krebs (4) Andere (12) Nicht angegeben (5)
Geschlecht: Median 82% weiblich
Alter: Median 54 Jahre
Länder : USA (107) UK (18) Australien (12) Kanada (10) Schweden (9) Niederlande (7) Weitere (35)
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Inhalte: Psychotherapie Einzel (55) Gruppe (42) Paar (10) Psychoedukation (19) Entspannungsverfahren (46) Einfache Informaationsgabe (23) Andere (12)
davon Einzel (119) Gruppe (66) Paar (8) Nicht angegeben (5)
Dauer/Frequenz/ Länge: 1-35 Sitzungen, Median 6 Sitzungen, Über 1-730 Tage, Median 42 Tage
Kontrollgruppen: TAU/UC Aufmerksamkeitskontrolle |
Primäre Endpunkte: 1. Distress 2. gesundheitsbezogene QoL 3. Depressivität 4. Angst |
1. Distress à Gesamteffekt Post-Intervention: 77 RCTs, N=? I2 = 73%; SMD=0.29 [0.20, 0.37, p <.001> Follow Up ≤6 Monate: 58 RCTs, N=? I2 = 56%; SMD=0.17 [0.09, 0.24, p <.001> Follow Up >6 Monate: 39 RCTs, N=? I2 = 32%; SMD=0.10 [0.04, 0.1, p =.003]
à Entspannungs-verfahren Post-Intervention: 11 RCTs, N=? I2 = 59%; SMD=0.29 [0.06, 0.52, p =.013] Follow Up ≤6 Monate: 4 RCTs, N=? I2 = 85%; SMD=0.66 [–0.12, 1.44, p=.10] Follow Up >6 Monate: 4 RCTs, N=? I2 = 56%; SMD=0.22 [–0.13, 0.56, p =.22]
2. QoL à Gesamteffekt Post-Intervention: 66 RCTs, N=? I2 = 78%; SMD=0.26 [0.15, 0.37, p <.001> Follow Up ≤6 Monate: 47 RCTs, N=? I2 = 65%; SMD=0.22 [0.12, 0.33, p <.001> Follow Up >6 Monate: 27 RCTs, N=? I2 = 50%; SMD=0.18 [0.07, 0.28, p <.001>
à Entspannungs-verfahren Post-Intervention: 8 RCTs, N=? I2 = 61%; SMD=0.35 [0.05, 0.65, p =.021] Follow Up ≤6 Monate: 5 RCTs, N=? I2 = 83%; SMD=0.78 [0.17, 1.4, p=.013] Follow Up >6 Monate: 1 RCT, N=? I2 = ?%; SMD=0.42 [ ?]
3. Depressivität à Gesamteffekt Post-Intervention: 72 RCTs, N=? I2 = 56.5%; SMD=0.33 [0.25, 0.41, p <.001> Follow Up ≤6 Monate: 40 RCTs, N=? I2 = 40.8%; SMD=0.2 [0.11, 0.28, p <.001> Follow Up >6 Monate: 26 RCTs, N=? I2 = 47.1%; SMD=0.14 [0.05, 0.24, p =.002]
à Entspannungs-verfahren Post-Intervention: 14 RCTs, N=? I2 = 74%; SMD=0.37 [0.09, 0.65, p =.009] Follow Up ≤6 Monate: 1 RCT, N=? I2 = ?; SMD=1.07 [ ?]
4. Angst à Gesamteffekt Post-Intervention: 74 RCTs, N=? I2 = 60%; SMD=0.38 [0.29, 0.46, p <.001> Follow Up ≤6 Monate: 38 RCTs, N=? I2 = 73%; SMD=0.34 [0.2, 0.47, p <.001> Follow Up >6 Monate: 15 RCTs, N=? I2 = 33%; SMD=0.17 [0.06, 0.28, p =.003]
à Entspannungs-verfahren Post-Intervention: 22 RCTs, N=? I2 = 75%; SMD=0.53 [0.29, 0.77, p <.001> Follow Up ≤6 Monate: 7 RCTs, N=? I2 = 93%; SMD=1.12 [0.31, 1.92, p=.007]
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Nicht berichtet |
Primärstudien: RCTs mit low RoB SB: 51 PB: kA DB: kA AB: 122 RB: 141 OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2, 7, 13 non-kritischer Dom. 3, 10,
Sensitivitäts-analysen: Bei hoher Heterogenität (l²>70%) Ausschluss vjew. einer Studie aus MA & Moderatorenanalysen (u.A. Alter, Tumorart)
Weiterhin a priori geplante Subgruppenanalysen (siehe Hauptergebnisse)
Publikations-bias: Visuelle Prüfung der Funnel-Plots
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Entspannungsverfahren und imaginative Verfahren RCTs (2015 – 2020)
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Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Patienten-merkmale |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Finanzierung / Conflict of Interest |
Methodische Bemerkungen |
Evidenzklasse |
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Unterstützende Evidenz (9/10) |
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Gregoire (2020) Effects of an intervention combining self-care and self-hypnosis on fatigue and associated symptoms in posttreatment cancer patients: A randomized-controlled trial. |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 95
ITT-Analyse mit multipler Imputation (LOCF) Ausgewertet: N = 95
Land: Belgien 2016-2019
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Nicht-metastasierender Krebs, primäre Behandlung vor < 1 Jahr
Geschlecht: 100% weiblich
Alter: 24-78 Mittelwert: 53.85 |
Arm A: N=48 SCH Self-care + Selbsthypnose (SCH) Gruppen-intervention,120 Minuten, 1x wöchentlich, 8 Wochen + eigenes Üben zwischen den Sitzungen
Arm B: N=47 WL Warteliste-kontrollgruppe, UC |
Erhebungszeitpunkte: Baseline Post-Intervention
Primäre Endpunkte: 1. Fatigue (MFI-20)
Sekundäre Endpunkte: 1. Schlaf-probleme (ISI) 2. Emotionaler Distress & Emotions-regulation; u.a. Angst & Depressivität (HADS, PSWQ, MAC) 3. Kognitive Funktion 4. Körperliche Aktivität |
MANOVA: Sign. Haupteffekt Zeit Sign. Zeit x Gruppen-Interaktion
1. Fatigue (General Fatigue) à SCH vs. WL Post-Intervention: Sign. Reduktion in der SCH (d=0.67)
2. Angst à SCH vs. WL Sign. Reduktion in der SCH von T1 zu T2 (d=0.67)
3. Depressivität à EG vs. KG Sign. Reduktion in der SCH von T1 und T2 (d=0.71)
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Arm A: EG UEs: kA
Arm B: KG SUEs: kA UEs: kA
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King Baudouin Foundation + Plan National Cancer of Belgium + Benoit Foundation + Belgian National Funds for Scientific Research Laut Angaben kein COI
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Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: low
Keine Fallzahlplanung. |
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Dikmen & Terzioglu et al., 2019: Effects of Reflexology and Progressive Muscle Relaxation on Pain, Fatigue, and Quality of Life during Chemotherapy in Gynecologic Cancer Patients |
RCT prospektiv, multizentrisch, blind, 4 Arme (3 x EG (CAM) + KG)
Randomisiert: N=140 Post-Intervention: N=80
Kein ITT, PP-Analyse; ausgewertet: N=80
Land: Türkei Dezember 2013 – Juli 2015 |
53 x Eierstockkrebs 18x anderer Krebs Stadium I-III
Geschlecht: 100% weiblich
EG & KG: Alter: 45 - 67 Median: 56.36 |
Arm A, B und C: NR=100 NP=60
Arm A: PMR, 20 Minuten, 2x wöchentlich, 8 Wochen
Arm B: Fußreflexzonenmassage (FRM), 30 Minuten, 2x wöchentlich, 8 Wochen
ARM C: PMR + FRM, 50 Minuten, 2x wöchentlich, 8 Wochen
ARM D: NR=40 NP=20 TAU |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up 1 (4 Wochen)
Primäre Endpunkte: 1. Schmerz (BPI) 2. Fatigue (BFI) 3. QoL (MQOLS-CA)
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1. Schmerz (pain severity) à PMR vs. FRM vs. PMR+FRM vs. TAU: Post-Intervention: Sign. Gruppenunterschied In PMR und TAU jedoch keine Verbesserungen über Zeit
2. Fatigue (fatigue severity): à PMR vs. FRM vs. PMR+FRM vs. TAU: Post-Intervention & FU1: Sign. Gruppenunterschied In PMR und TAU jedoch keine Verbesserungen über Zeit
3. QoL à PMR vs. FRM vs. PMR+FRM vs. TAU: Post-Intervention & FU1: Sign. Gruppenunterschied In PMR und TAU jedoch keine Verbesserungen über Zeit
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Arm A: PMR UEs: 0
Arm B: FMR SUEs: 0 UEs: 0
Arm C: PMR+FMR SUEs: 0 UEs: 0
Arm D: TAU SUEs: 0 UEs: 0
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Die Studie wurde vollständig finanziert Vom Department of Midwifery, Faculty of Health Sciences, Selcuk University, Konya, Türkei, Department of Nursing, Faculty of Health Sciences, Atilim University, Ankara, Türkei
Keine COI angegeben |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: high RB: unclear
Geplante Fallzahl (N=80) erreicht
Darstellung der Ergebnisse mangelhaft, keine Post-Hoc Vergleiche zu Between-Group-Omnibustests,
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Gok Metin (2019): Effects of progressive muscle relaxation and mindfulness meditation on fatigue, coping styles, and quality of life in early breast cancer patients: An assessor blinded, three-arm, randomized controlled trial. |
RCT prospektiv, monozentrisch, offen, 3 Arme
Randomisiert: N = 92 Post-Intervention : N=87
ITT-Ansatz, kA zu Imputationsverfahren Ausgewertet: N = 92 Land: Türkei 2018-2019 |
Brustkrebspatientinnen (Stadien I-III)
Geschlecht: 100% weiblich
Alter: Mittelwert 49.25
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Arm A: NB=31 NP=28 PMR, einmalig 40 Minuten + Broschüre, tägliches Üben, 12 Wochen
Arm B: NB=32 NP=31 Achtsamkeits-Meditation (MM), einmalig 40 Minuten + Broschüre, tägliches Üben, 12 Wochen
Arm C: NB=29 NP=28 Aufmerksamkeits-Kontrollgruppe (AC) 1x 15 Minuten allg. Brustkrebs-Edukation
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Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (2 Wochen)
Primäre Endpunkte: 1. Fatigue (BFI)
Sekundäre Endpunkte: 1. Coping (COPE) 2. QoL (FLIC) |
1. Fatigue (Total BFI) à PMR vs. MM vs. AC Post-Intervention: Sign. Gruppenunterschied zwischen PMR und MM vs. AC zugunsten von PMR & MM
2-Wochen-Follow-Up: Sign. Gruppenunterschied zwischen PMR und MM vs. AC zugunsten von PMR & MM
2. QoL à PMR vs. MM vs. AC |
Arm A: PMR UEs: kA
Arm B: MM SUEs: kA UEs: kA
Arm C: AC SUEs: kA UEs: kA
„Moreover, no participants dropped out owing to unexpected adverse events of PMR or MM, indicating that both interventions were safe and well-tolerated by patients with EBC.“ (S. 121)
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Scientific Reseach Projects coordination Unit of Hacettepe University (Türkei)
Laut Angaben kein COI
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Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Post-hoc Power-Analyse. |
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Parsa Yekta (2017): Techniques on Postoperative State Anxiety in Candidates for The Mastectomy Surgery: A Randomized Controlled Clinical Trial. |
RCT prospektiv, monozentrisch, offen, 3 Arme
Randomisiert: N = 90
Ausgewertet: N = 90
Land: Iran 2013-2014
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Mastektomiepatientinnen
Geschlecht: 100% weiblich
Alter: 30-50 71,1% < 50 28,9% > 50
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Arm A: N=30 Benson Meditation, 20 Minuten, 3x am Tag vor der Masektomie
Arm B: N=30 Rhythmisches Atmen, 20 Minuten, 3x am Tag vor der Masektomie
Arm C: N=30 KG Keine Intervention
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Erhebungszeitpunkte: Baseline Post-Intervention (Post-OP)
Primärer Endpunkt: 1. Angst (CSAQ) |
1. Angst àBenson Meditation vs. KG: Post-Intervention: Sign. Gruppenunterschiede zugunsten von Bensons Meditation
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Arm A: UEs: kA
Arm B: SUEs: kA UEs: kA
Arm C: SUEs: kA UEs: kA |
Tehran University of Medical Sciences
Laut Angaben kein COI |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N = 28 pro Gruppe) erreicht. |
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Shahriari (2017): Effects of progressive muscle relaxation, guided imagery and deep diaphragmatic breathing on quality of life in elderly with breast or prostate cancer. |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 50
kA zu Umgang mit Dropouts Ausgewertet: N = 50
Land: Iran Mai – Dezember 2014 |
Brust- oder Prostata-krebs
Geschlecht: 28% weiblich
Alter: Mittelwert: 66 |
Arm A: N=25 PMR, gelenkte Imagination & Zwerchfellatmung, 45 Minuten, 8 Sitzungen, 4 Wochen + 6 Wochen selbstständige Anwendung
Arm B: N=25 CAU + 3 Sitzungen "Lifestyle Intervention"
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Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (6 Wochen)
Primärer Endpunkt: 1. QoL (EORTC QLQC30) |
1. QoL à PMR vs. CAU Post-Intervention: Sign. Gruppenunterschied zugunsten PMR
6 Wochen Follow-Up: Sign. Gruppenunterschied zugunsten PMR
In PMR Zunahme von QoL, in CAU Abnahme von QoL über die Zeitpunkte |
Arm A: PMR UEs: kA
Arm B: CAU SUEs: kA UEs: kA |
School of Nursing and Midwifery, Isfahan University of Medical Sciences
Laut Angaben kein COI |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N = 25 pro Gruppe) erreicht. |
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Charalambous et al., 2016: Guided Imagery And Progressive Muscle Relaxation as a Cluster of Symptoms Management Intervention in Patients Receiving |
RCT prospektiv, multizentrisch, offen, 2 Arme
Randomisiert: N=236 Post-Intervention: N = 208
Completer-Only-Analyse Ausgewertet: N=208
Land: Griechenland Januar 2011-Dezember 2012 |
Brustkrebspatientinnen (50%), Prostatakrebspatienten (50%), Stadium III
Geschlecht: 50% weiblich
EG & KG: Alter: 31- >60 Mittelwert: (kA) |
Arm A: N=120 PMR + geleitete Imagination, 30min, 4x wöchentlich, 4 Wochen
Arm B: N=116 TAU |
Erhebungszeitpunkte: Baseline Post-Intervention
Primärer Endpunkt: 1. Depressivität (BDI-II) 2. Fatigue (CFS) 3. Angst (SAS) 4. Übelkeit (INVR)
Sekundäre Endpunkte: 1. QoL (EORTC QLQ-C30) 2. Funktionsniveau (physisch, kognitiv, sozial) 3. Atemlosigkeit 4. Schlaflosigkeit 5. Apettitlosigkeit 6. Durchfall 7. Finanzielle Probleme 8. Verstopfung 9. Schmerz (NRS, 10-stufig)
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Hauptergebnisse:
1. Depressivität à PMR vs TAU Post-Intervention: Sign. Haupteffekt Zeit und Zeit x Gruppe-Interaktion
2. Fatigue à PMR vs TAU Post-Intervention: Sign. Zeit x Gruppe-Interaktion
3. Angst à PMR vs TAU Post-Intervention: Sign. Zeit x Gruppe-Interaktion
4. Übelkeit: à PMR vs TAU Post-Intervention: Post-Intervention: Sign. Haupteffekt Gruppe und Zeit x Gruppe-Interaktion
5. QoL à PMR vs TAU Post-Intervention: Sign. Haupteffekt Gruppe und Zeit x Gruppe-Interaktion
6. Schmerz à PMR vs TAU Post-Intervention: Sign. Haupteffekt Gruppe und Zeit x Gruppe-Interaktion
è Alle Zeit x Gruppe Interaktionen zugunsten der IG
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Keine berichtet |
Die Studie wurde vollständig finanziert von der Cyprus University of Technology (INT-480619-2010).
Keine COI angegeben |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: high RB: low
Geplante Fallzahl (N = 256) nicht erreicht.
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Thuma (2016): Hypnosis as an Adjunct for Managing Pain in Head and Neck Cancer Patients Post Radiotherapy. |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 68 Post-Intervention : N=65
PP-Analyse Ausgewertet: N = 65
Land: Thailand 2015-2016
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Kopf- und HalskrebspatientInnen, nach Radiotherapie
Geschlecht: 63.2 % weiblich
Alter: 41-70 Mittelwert: 55.85 |
Arm A: NB = 34 NP = 33 Hypnose 1 Sitzung à 20 Minuten am 4. Tag nach Bestrahlung
Arm B: NB = 34 NP = 32 Keine Intervention
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Erhebungszeitpunkte: Baseline Post-Intervention
Primärer Endpunkt: 1. Schmerz (VAS) |
1. Schmerz à Hypnose vs. KG Post-Intervention:
Gruppe als sign.r Prädiktor in linearer Regression mit anderen Variablen (Baseline-Wert, Geschlecht, Alter, Opioidgebrauch) zugunsten von Hypnose
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Arm A: Hypnose UEs: 0/34
Arm B: KG SUEs: 0/34 UEs: 0/34 |
Keine Angabe zur Finanzierung
Laut Angaben kein COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: low RB: unclear
Post-hoc-Poweranalyse |
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Zgaia (2016): The impact of relaxation technique and pre-operative psychological counselling on pain, analgesic consumption and psychological symptoms on patients scheduled for breast cancer surgery – a randomized clinical study. |
RCT prospektiv, monozentrisch, offen, 2 Arme ITT-Analyse
Randomisiert: N = 102 Post-Intervention: N=102
ITT-Ansatz Ausgewertet: N = 102
Land: Rumänien 2015 |
Brustkrebspatientinnen
Geschlecht: 100% weiblich
Alter: Mittelwert 55.6 |
Arm A: NB=58 NP=52 Präoperative Entspannungstechnik (Entspannung und PC (psychologische Beratung) 1 Sitzung 25 Minuten Interview und 25 Minuten autogenes Training
Arm B: NB=44 NP=50 Keine Intervention |
Erhebungszeitpunkte: Baseline Post-Intervention (Post-OP) FU1 (2h) FU2 (8h) FU3 (12h) FU4 (24h) FU5 (30h) FU6 (36h) FU7 (48h)
Primäre Endpunkte: 1. Schmerz (NRS) 2. Distress (Belastung durch psychische Symptome) |
1. Postoperativer Schmerz à IG vs. KG Post-Intervention, FU1- 6: Sign. weniger Schmerz in der IG Kein sign.r Unterschied zu FU7
2. Distress à IG vs. KG Post-Intervention, FU1, 2, 3, 4, 5, 7: Sign. geringere psychologische Symptome
Kein sign.r Unterschied in FU6
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Arm A: IG UEs: kA
Arm B: KG SUEs: kA UEs: kA |
Keine Angabe zur Finanzierung
Keine Angabe bzgl. COI |
Risk of Bias
SB1: high SB2: high PB: high DB: high AB: unclear RB: unclear
Geplante Fallzahl (N = 50 pro Gruppe) erreicht zu |
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Chen et al. 2015: Effect of Relaxation With Guided Imagery on The Physical and Psychological Symptoms of Breast Cancer Patients Undergoing Chemotherapy |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=65 Post-Intervention: N=65
kA zu Umgang mit Dropouts Ausgewertet: N=65
Land: Taiwan 2011-2012 |
Brustkrebs Patientinnen, Stadium II-IV, anstehende Chemotherapie
Geschlecht: 100% weiblich
EG Alter: 40-59 Median: 49.3
KG Alter: 41-63 Median: 52.3 |
Arm A: NB=32 NP=32 Einmaliges Entspannungstraining mit geführter Imagination (GUI) vor Chemo, 60min + CD mit 20min Imagination für 7 Tage
Arm B: NB=33 NP=33 TAU
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Erhebungszeitpunkte: Baseline Post-Intervention
Primärer Endpunkt: 1. Angst (HADS-A) 2. Depressivität (HADS-D) 3. Distress (SDS)
Sekundäre Endpunkte (weitere Variablen mit SDS): 1. Schmerz 2. Übelkeit 3. Erbrechen 4. Xerostomie 5. Mukositis 6. Dysphagie 7. Verstopfung 8. Durchfall 9. Schlaflosigkeit 10. Fatigue 11. Dyspnoe 12. Engegefühl in der Brust 13. Husten 14. Abdominales Völlegefühl 15. Sodbrennen 16. Unaufmerksam 17. Taubheitsgefühl
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Prätest-Posttest-Vergleich nach durchgeführter Chemotherapie: 1. Angst à GUI vs TAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten GUI
2. Depressivität à GUI vs TAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten GUI
3. Distress à GUI vs TAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten GUI
4. Schmerz à GUI vs TAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten GUI
5. Übelkeit à GUI vs TAU: Post-Intervention: Keine sign. Gruppenunterschiede
6. Fatigue à GUI vs TAU: Post-Intervention: Keine sign. Gruppenunterschiede |
Keine berichtet |
MacKay Memorial Hospital Zweigstelle Tamshui in Taiwan
Keine COI angegeben |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: low RB: unclear
Geplante Fallzahl erreicht (N=60, 30 pro Arm)
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|
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Evidenz zu Ungunsten der Intervention (1/10) |
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Amraoui et al. 2018: Effects of a Hypnosis Session Before General Anesthesia on Postoperative Outcomes in Patients Who Underwent Minor Breast Cancer Surgery: The HYPNOSEIN Randomized Clinical Trial. |
RCT prospektiv, multizentrisch, verblindet (Patienten), 2 Arme
Randomisiert: N=150 Post-Intervention & FUs: N=148
ITT-Ansatz ohne Imputation Ausgewertet: N=148
Land: Frankreich 2014 – 2015 |
Mamma-Ca-Patientinnen, angemeldet für brust-erhaltende OP
Geschlecht: 100% weiblich
IG Alter: 33-79 Median: 57
KG Alter: 20-84 Median: 53 |
Arm A: NB=77 NP=77 NFU1=77 NFU2=77 NFU3=77 Individuelle Hypnose, einmalig kurz vor OP, 2-15min, M=6min
Arm B: NB=73 NP=71 NFU1=71 NFU2=71 NFU3=71 TAU
Gleiche anästhesistische Behandlung beider Gruppen |
Erhebungszeitpunkte: Baseline Post-Intervention (Post-OP) Follow-Up 1 (1 Tag) Follow-Up 2 (7 Tage) Follow-Up 3 (30 Tage)
Primärer Endpunkt: 1. (Brust-) Schmerz (VAS)
Sekundäre Endpunkte: 2. Fatigue (VAS) 3. Well-Being (VAS) 4. Angst (VAS) |
Nach Brustkrebs-operation: 1. (Brust-) Schmerz à Hynose vs TAU: Sign. geringer in TAU Follow-Ups: Keine sign.n Gruppenunterschiede
2. Fatigue à Hynose vs TAU: Post-Intervention: Keine sign.n Gruppenunterschiede Follow-Ups: Keine sign.n Gruppenunterschiede
3. Angst à Hynose vs TAU:
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Keine Neben & Wechselwirkungen angegeben |
Montpellier Cancer Institute (ICM)
1/10 Studienärzten erhielt extern Geldmittel von Grünenthal |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: low AB: low RB: high
Geplante Fallzahl nicht erreicht (N=150)
|
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Psychoedukation
|
Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Merkmale untersuchter Studien |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Methodische Bemerkungen |
Evidenzklasse |
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|
Sanjida et al. 2018: "Are psychological interventions effective on anxiety in cancer patients? A systematic review and meta-analyses."1
Eingeschlossene Primärstudien: 71 Primärstudien in qual. Review / 51 in Meta-Analysen |
SysRev & MA
Suchzeitraum: Januar 1993– Juni 2017
Datenbanken: CENTRAL Medline Embase CINAHL Scopus PsycInfo
Einschluss-kriterien: P: erwachsene Krebspatienten I: psychosoziale Intervention C: alternative Intervention, TAU/UC, Warteliste O: Angst, Distress S: RCTs
71 RCTS, N=13098 Patientinnen
51 RCTs, N=8283 Patientinnen in MA
|
RCTs
Brustkrebs (36) Gynäkologische Tumore (3) Prostata- und Hodenkrebs (2) Sonstige Krebsidiagnosen (29)
Geschlecht: 74,6% weiblich
Mittleres Alter: 55
Länder : USA (19) Europa (29) Weitere (53)
|
Inhalte: 14 x CBT 12 x Entspannungs-verfahren 9x Psychosoziale Therapie 13x "Supportive Care Interventions" 3x gestufte Interventionen ("stepped care") 20x sonstige
Dauer/Frequenz/ Länge: 4 Tage – ein Jahr
Kontrollgruppen: alternative Intervention TAU/UC Warteliste |
Primäre Endpunkte: 1. Angst
Verwendete Messinstrumente: Angst HADS STAI POMS
|
1. Angst àGesamteffekt: Post-Intervention: 51 RCTs, n=7491 I2 = 68%; SMD=–0.21 [–0.30, –0.13, p < .001] à Sensitivitätsanalyse: Entfernung der Studie mit größtem und kleinsten Effekt, keine Änderung des Ergebnis
àPsychoedukation: Post-Intervention: 5 RCTs, I2 = 42%; SMD=–0.18 [–0.36, –0.01, p <.05>
|
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 18 PB: 2 DB: 7 AB: 42 RB: 48 OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 7,11,15 non-kritischer Dom. 5,8
Sensitivitäts-analysen: durchgeführt, siehe Hauptergebnisse
Durchführung von Subgruppen-analysen, teilweise in Hauptergebnissen aufgeführt
Publikations-bias: "Studies with a sample size of less than 40 participants were excluded to reduce the potential influence of publication bias and inflated ES common in small studies." |
1a |
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|
Kalter et al. 2018: "Effects and moderators of psychosocial interventions on quality of life, and emotional and social function in patients with cancer: An individual patient data meta-analysis of 22 RCTs." 5
Eingeschlossene Primärstudien: 61 RCTs, davon 22 in IPD-Meta-Analyse Armes 2007 Arving 2007 Braamse 2015 Chambers 2013 Duijts 2012 Ell 2008 Ferguson 2012 Gellaitry 2010 Gielissen 2006 Goedendorp 2010 Graves 2003 Heiney 2003 Johansson 2008 Kimman 2011 Mann 2012 Meneses 2007 Northouse 2005 Nothouse 2007 Northouse 2013 Savard 2005 Savard 2006 Van der Berg 2015
|
IPD MA
Suchzeitraum: Bis Oktober 2017
Datenbanken: Medline Embase CINAHL PsycInfo
Einschluss-kriterien: P: erwachsene Krebspatienten I: Informations-vermittlung, Support, CST, Psychotherapie C: TAU/UC, Warteliste, Aufmerksamkeits-placebo O: QoL + weitere Outcomes S: RCTs
22 RCTs, N=4217 Patientinnen in IPD-MA |
RCTs
Brustkrebs (13) Hämatologischer Krebs (1) Prostatakrebs (2) Gemischte Krebsidiagnosen (6)
Geschlecht: 65% weiblich
Mittleres Alter: 56 (SD=11.4)
Länder : USA (8) Niederlande (6) Kanada (2) Schweden (2) Australien (1) UK (3)
|
Inhalte: CST (19) Psychotherapie (2) Informations-vermittlung (1) Support (-)
Dauer/Frequenz/ Länge: 4-52 Wochen 1-54 Sitzungen (teils Langzeit-einzeltherapie)
Individual-, Gruppen-, und Paarsetting
Kontrollgruppen: TAU/UC (14) Warteliste (6) Aufmerksamkeits-placebo (2) |
Primäre Endpunkte: 1. QoL
Sekundäre Endpunkte: 1. Emotionales Funktion-niveau 2. Soziales Funktionsniveau
Verwendete Messinstrumente: QoL FACT-G QLQ-C30 SF-36 QoL-CS
|
1. QoL à Gesamteffekt: Post-Intervention: 22 RCTs, n=4217 SMD=0.14 [0.06, 0.21, p<.05>
Interventionstyp als sign. Moderator (p=.01): àInformations-vermittlung: Post-Intervention: 1 RCT, SMD=0.19 [0.03, 0.34, p <.05>
|
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 15 PB: nicht erfasst DB: nicht erfasst AB: 17 RB: 18 OB: kA "Items related to blinding were omitted because blinding of patients and personnel is difficult in case of a PSI. Also, the rating of blinding of outcome assessors was excluded because QoL, EF, and SF were assessed using patient‐reported outcomes (PROs)." (p.1153)
Review: AMSTAR-2: low quality Method.Mängel in kritischer Domäne 7 non-kritischer Dom. 3,12,14
Sensitivitäts-analysen: Durchführung von Moderatoren-analysen, teilweise in Hauptergebnissen aufgeführt
Publikations-bias: Visuelle Prüfung Funnel-Plot + Egger's Test / keine Hinweise auf Publication Bias
|
1a |
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Hsieh et al. 2017: "The effects of supportive care interventions on depressive symptoms among patients with lung cancer: A metaanalysis of randomized controlled studies."12
Eingeschlossene Primärstudien: Bredin 1999 Wu 2003 Chen 2006 Ni 2009 Carlson 2010 Porter 2011 Yao 2012 Walker 2014 Badr 2015 Morano 2014 Chen 2015 Molassiotis 2015a, b
|
MA
Suchzeitraum: September 2015
Datenbanken: Embase Pubmed CENTRAL CEPS
Einschluss-kriterien: P: Lungenkrebs I: "supportive care": nicht-pharmakologisch, nicht invasiv, Förderung und Erhaltung von Wohlbefinden und Krankheitsverarbeitung C: TAU/UC O: Depressivität S: RCTs
12 RCTs, N=1472 Patientinnen
|
RCTs
Lungenkrebs, Stadien I-IV, teils komorbide COPD, eine Studie mit komorbider Depression als Einschluss-kriterium
Geschlecht: kA
Alter: 56 - 71
Länder : China (4) UK (3) USA (2) Kanada (1) Brasilien (1) Taiwan (1)
|
Inhalte: CBT + Psychoedukation (5) Psychoedukation (4) Sport- und Bewegungstherapie (3)
davon Face-to-face (8) Telefon (4)
Dauer/Frequenz/ Länge: 6 – 60 Sitzungen 4 -32 Wochen
Kontrollgruppen: Tau/UC (10) Edukation (2) |
Primäre Endpunkte: 1. Depressivität
Verwendete Messinstrumente: Depressivität SDS PSSCAN-D BDI SCL-90 (depression score) HADS PROMIS |
1. Depressivität àGesamteffekt: Post-Intervention: 12 RCTs, N=1472 I2 = 88%; SMD=–0.75 [–1.07, –0.41, p <.001>
àPsychoedukation: Post-Intervention: 4 RCTs, N=770 I2 = 92%; SMD=–0.39 [–0.94, 0.15 ]
|
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 7 PB: ka DB: 8 AB: 8 RB: kA OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7,15 non-kritischer Dom. 3,5,10
Sensitivitäts-analysen: Schrittweiser Ausschluss kleiner (N<50) Studien und Studien mit High-RoB führten zu keiner Änderung der Ergebnisse
Publikations-bias: "Finally, the existence of a publication bias cannot be ignored. It should be noted that publication bias has some effect on the available evidence pool." (p. 721)
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1a- |
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Bennett et al., 2016: "Educational interventions for the management of cancer-related fatigue in adults."
Eingeschlossene Primärstudien: Reif 2012 Wangnum 2013 Yun 2012 Yates 2005 Ream 2006 Purcell 2011 Godino 206 Schjolberg 2014 Yuen 2006 Barsevick 2004 Barsevick 2010 Foster 2015 |
CochraneRev
Suchzeitraum: Bis Oktober 2016
Datenbanken: CENTRAL MEDLINE EMBASE CINAHL PsycINFO ERIC OTseeker PEDro ClinicalTrials.gov Australian New Zealand Trials Registry
Einschluss-kriterien: P: erwachsene Krebspatienten I: edukative Interventionen für CRF C: alternative Intervention, TAU/UC, Warteliste O: Fatigue S: RCTs
14 RCTs, N=2213 Patientinnen
|
RCTs
9 x gemische Krebsdiagnosen 3 x Brustkrebs 1 x Lungenkrebs 1 x Dickdarm- oder Magenkrebs
Geschlecht: kA
Alter: Durschnitt bei ~50
Länder: USA (19) Europa (29) Weitere (53)
|
Inhalte: 4x Informations-vermittlung 10x Informations-vermittlung + behaviourale Techniken
davon 8x face-to-face 2x internetbasiert 4x telefonbasiert
Dauer/Frequenz/ Länge: 2- 9 Sitzungen Median 30min pro Sitzung
Kontrollgruppen: alternative Intervention TAU/UC Warteliste |
Primäre Endpunkte: 1. Fatigue (global) 2. Fatigue Intensität 3. Fatigue Distress 4. Beeinträchtigung durch Fatigue
Sekundäre Endpunkte: 5. Fatigue Management 6. Alltagsfunktions-niveau 7. Angst 8. Depressivität 9. QoL
Verwendete Messinstrumente: Fatigue FACT-F FAQ MFI GFS PFS Total Score VAS |
1. Fatigue (global) àGesamteffekt: Post-Intervention: 12 RCTs, n=1680 I2 = 80%; SMD=-0.27 [–0.51, –0.04, p=.02] GRADE: low quality Subgruppenanalyse ergab keine Unterschiede
2. Angst àGesamteffekt: Post-Intervention: 3 RCTs, n=571 I2 = 76%; MD=-1.47 [–2.76, –0.18, p=.03] Skala von 0–21 GRADE: low quality
3. Depressivität àGesamteffekt: Post-Intervention: 4 RCTs, n=881 I2 = 85%; SMD=–0.12 [–0.47, 0.23, p=.50] GRADE: very low quality
4. QoL àGesamteffekt: Post-Intervention: 2 RCTs, n=477 I2 = 87%; MD=11.47 [1.29, 21.65, p=.03] Skala von 0–100 GRADE: low quality
|
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 11 PB: k.a. DB: 0 AB: 2 RB: 14 OB: 14
Review: AMSTAR-2: high quality Method.Mängel in kritischer Domäne - non-kritischer Dom. 3
Sensitivitäts-analysen: Geplant, aber für rel. Outcomes nicht durchgeführt
A priori geplante Subgruppenanalyse (siehe Hauptergebnisse)
Publikations-bias: In GRADE-Bewertung eingeflossen |
1a |
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De Boer et al. 2015
„Interventions to enhance return-to-work for cancer patients“
Eingeschlossene Primärstudien: Ackerstaff 2009 Berglund 1994 Burgio 2006 Emmanouilidis 2009 Friedrichs 2010 Hillman 1998 Hubbard 2013 Johnsson 2007 Kornblith 2009 Lee 1992 Lepore 2003 Maguire 1983 Purcell 2011 Rogers 2009 Tamminga 2013
|
CochraneRev
Suchzeitraum: Bis März 2014
Datenbanken: CENTRAL Medline EMBASE CINAHL OSH-ROM & OSH-Update PsycINFO DARE ClinicalTrials.gov Trialregister.nl Controlled-trials.com
Einschluss-kriterien: P: Erwachsene mit Krebsdagnose, in Beschäftigungsverhätnis zum Zeitpunkt der Diagnose I: jegliche Intervention mit dem Ziel RTW (return to work) zu verbessern C: - O: RTW, QOL S: RCTs, cluster-RCTs
15 RCTs, N=1835 Patientinnen
|
RCTs
Brustkrebs (7) Prostatakrebs (2) Schilddrüsenkrebs (1) Gynäkologisch (1) Kopf- und Halskrebs (1) Kehlkopf (1) Leukämie (1) Gemischt (1)
Geschlecht: kA
Alter: kA
Länder : USA (5) Europa (9) Australien (1)
|
Inhalte: Psychoedukation (2) Sport (1) Medizinisch (7) Multidisziplinär (5)
Dauer/Frequenz/ Länge: kA
|
Primäre Endpunkte: 1. RTW
Sekundäre Endpunkte: 1. QoL
Verwendete Messinstrumente: QoL EORTC QLQ-C30, SF-36, EQ-5D, FACT-B
|
1. QoL àPsychoedukation: Post-Intervention, Komparator CAU: 2 RCTs, N=260 SMD=0.05 [–0.2, 0.3, p>.05] GRADE: "low quality evidence of no difference" (Leopore 2003, Purcell 2011)
|
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB PB: 1 DB: 1 AB: 11 RB: 14 OB: 0
Review: AMSTAR-2: moderate quality Method.Mängel in kritischer Domäne - non-kritischer Dom. 12,14
Sensitivitäts-analysen: "We intended to analyse how sensitive our results were to the risk of bias in the included studies. However, there was an insuEicient number of studies available per comparison to do such an analysis." (p.11)
Publikationsbias: Visuelle Prüfung Funnel-Plot, bei rel. Vergleich wegen geringer Studienzahl nicht durchgeführt |
1a |
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Jho et al. 2013: "Efficacy of pain education in cancer patients A meta-analysis of randomized controlled trials."
Eingeschlossene Primärstudien: Dalton 1986 De Wit 2001 Chang 2002 Lai 2004 Yates 2004 Keefe 2005 Vallières 2006 Ward 2008, 2009 Yildirim 2009 Kravitz 2011 Wilkie 2010
|
MA
Suchzeitraum: Bis Februar 2012
Datenbanken: CENTRAL PubMed Embase
Einschluss-kriterien: P: Krebspatienten mit Schmerzen I: Aufklärung / Intervention zur Behandlung von Krebsschmerzen C: TAU/UC, Standard-Schmerzerziehung, Aufmerksamkeitsplacebo O: Schmerz S: RCTs
Studien mit "high risk of bias" ausgeschlossen!
12 RCTs, N=2169 Patienten
|
RCTs
8x versch. Krebsdiagnosen 1x Brustkrebs 1x Lungenkrebs
Geschlecht: 59 % weiblich
Mittleres Alter: 57.2 Jahre
Länder : USA (6) Niederlande (1) Australien (1) Türkei (1) Kanada (1) Taiwan (2) |
Inhalte: 11x Face-to-Face Schmerzedukation (5x mit zusätzl. Telefonanruf) 1x Telefonanruf
davon 11x zusätzl. Informations-material
Dauer/Frequenz/ Länge: kA, vermtl. Kurzintervention mit Telefon-Follow-Up
Kontrollgruppen: 6x TAU/UC 3x Aufmerksam-keitsplacebo 2x Standard Schmerzedukation |
Primäre Endpunkte: 1. Schmerz
Verwendete Messinstrumente: Schmerz NRS VAS |
1. Schmerz à Gesamteffekt: Postintervention: 12 RCTS I² = 27%; SMD=-0.11 [–0.20, –0.02, p<.001>
|
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 12 PB: 9 DB: 12 AB: 7 RB: 5 OB: kA Methodische Qualität der Primärstudien bewertet anhand der Jadad Skala (n =12)
Review : AMSTAR-2: Critically low quality Method.Mängel in kritischer Domäne 2,7,9,13,15 non-kritischer Dom. 1,3,8,10,12,14
Sensitivitäts-analysen: Nicht durchgeführt
Publikationsbias: Nicht addressiert
|
1a-
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Marie et al. 2013: "Optimal patient education for cancer pain: a systematic review and theory-based meta-analysis."
Eingeschlossene Primärstudien: Arathuzik, 1994, Aubin et al., 2006 Borneman et al., 2011, Bozcuk et al., 2003 Change et al., 2002 Dalton, 1987 De Wit, 2001 Kim et al., 2004 Lai et al., 2004 Lovell et al., 2010 Ward et al., 2010 Ward et al., 2009 Ward et al., 2000 Yates et al., 2004 Kravitz et al., 2011 Regan et al., 2000 Dalton et al., 1994 |
MA
Suchzeitraum: Bis Mai 2012
Datenbanken: Referenzliste früherer Artikel MEDLINE PsycINFO CENTRAL
Einschluss-kriterien: P: Krebspatienten mit Schmerzen I: Schmerz-edukation C: TAU/UC O: Schmerz-intensität S: RCT
15 RCTs
|
RCTs
Eingeschlossen : mehrheitlich Bruskrebs
Geschlecht: Mehrheitlich weiblich
Mittleres Alter: 58
Länder: kA
|
Inhalte: 15x Schmerzedukation (unterschiedliche Elemente)
Dauer/Frequenz/ Länge: k.A.
Kontrollgruppen: Usual Care
|
Primäre Endpunkte: 1. Schmerz
Verwendete Messinstrumente: kA |
1. Schmerz à Gesamteffekt: 15 RCTs I²=71%, SMD=-0.27 [–0.47, -0.07, p<.01>
|
Keine SUEs berichtet |
Primärstudien: "Bias rating concluded that all studies were at high risk of bias." (p. 3532)
Review : AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,11,13,15 non-kritischer Dom. 3,8,10,12,14,16
Sensitivitäts-analysen: Geplanter Subgruppenvergleich (low RoB vs all) entfällt, da keine Studien mit low RoB
Publikationsbias: Nicht addressiert |
1a- |
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Oldenmenger et al. 2018: " A systematic review of the effectiveness of patient-based educational interventions to improve cancer-related pain."2
Eingeschlossene Primärstudien: Jahn 2013 Koller 2013 Kravitz 2012 Lai 2004 Lin 2006 Lovell 2010 Miaskowski 2004 Kim 2004 Oldenmenger 2011, 2017 Van der Peet 2009 Rustoen 2012, 2013 Smith 2010 Syrjala 2008 Thomas 2012 Tse 2012 Vallieres 2006 Ward 2008 Ward 2009a, b Wells 2003 Wilkie 2010 Williams 2015 De Wit 1997 EJP 2001 Wright Oliver 2001 Yildrim 2009 |
SysRev
Suchzeitraum: Januar 1995 – Mai 2017
Datenbanken: Medline CINAHL
Einschluss-kriterien: P: erw. Patienten mit krebsbedingtem Schmerz, nur solide Tumore I: Psycho-edukation mit Fokus auf Schmerz-management C: keine Intervention, aktive Kontrolle O: Schmerzinten-sität, Schmerzbeeinträchtigung, Wissen über Schmerz & Schmerzbarrieren, Medikationsadhärenz, Selbstwirksamkeit S: RCTs
26 RCTS, N=4735 Patienten
|
RCTs
Ambulante Patienten (20) & stationäre Patienten (5)
Krebsdiagnosen :
Geschlecht: kA
Mittleres Alter: kA
Länder : USA (12) Europa (8) Asien (3) Australien (2) Kanada (1)
|
Inhalte: 22 x Face-to-Face
5 x mehrere Sitzungen 4x mehrere Sitzungen + Telefongespräche, 3x einmaliger Kontakt 10x einmaliger Kontakt + Telefongespräche
3x Broschüre/Video davon 2x kombiniert mit Telefongesprächen
Dauer/Frequenz/ Länge: 5min – 90 min 1 Tag – 6 Wochen Frequenz sehr unterschiedlich (einmalig, merhmals pro Woche/Monat, Telefon Follow-Up)
Kontrollgruppen: TAU/UC, Ernährungsbera-tung, Pharmakotherapie, alternatives Schm.-Programm, Aufmerksamkeits-placebo
|
Primäre Endpunkte: 1. Schmerz 2. Schmerz-beeinträch-tigung
Sekundäre Endpunkte 1. Wissen über Schmerz & Schmerz-barrieren 2. Medikations-adhärenz 3. Selbstwirk-samkeit
Verwendete Messinstrumente: Schmerzintensität BPI NRS VAS |
1. Schmerz à Gesamteffekt: 8/26 Studien (31%) berichten statistisch signifikante Schmerzunterschiede zwischen den Gruppen zugunsten der Interventionsgruppe (19% der eingeschlossenen Patienten)
6 dieser Studien bestanden aus Face-to-Face-Kontakten + Face-to-Face oder Telefon Follow-Up |
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 12 PB: 1 DB: 3 AB: 5 RB: 22 OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7 non-kritischer Dom. 3,8,14
Sensitivitäts-analysen: Keine MA
Publikations-bias: nicht addressiert
|
1a |
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Du et al., 2015 "Patient education Programmes for cancer-related fatigue: A systematic review."
Eingeschlossene Primärstudien: Björneklett 2012 Chan 2011 Godino 2006 Kwekkeboom 2012 O’Brien 2014 Purcell 2011 Ream 2006 Reif 2013 Yates 2005 Yun 2012 |
SysRev
Suchzeitraum: bis April 2014
Datenbanken: Medline Pubmed Web of Science Elsevier CINAHL CENTRAL
Einschluss-kriterien: P: erwachsene Krebspatienten I: Edukation C: Warteliste Placebo, TAU/UC, Sport- & Bewegung O: Fatigue als Primäroutcome S: RCTS
10 RCTs, N=1498 Patientinnen
|
RCTs
6x versch. Krebstyp 1x Lungenkrebs, 2x Brustkrebs 1x Dickdarm- oder Magenkrebs
Geschlecht: kA
Alter: kA
Länder : China (1) Schweden (1) Spanien (1) UK (1) USA (1) Korea (1) Australien (3) Deutschland (1)
|
Inhalte: Edukations-programme (8x face-to-face in Gruppe, 1x Einzelsetting, 1x internet-basiert)
Dauer/Frequenz/ Länge: 1-12 Wochen 1-6 Sitzungen Follow-Up-Zitrüume 2 Wochen – 12 Monate
Kontrollgruppen: TAU/UC Warteliste Basisaufklärung |
Primäre Endpunkte: 1. Fatigue
Verwendete Messinstrumente:
|
1. Fatigue 2/10 Studien zeigten sign. positiven Effekt (mittlere ES) zugunsten der IG
3/10 Studien zeigten sign. positiven Effekt (kleine ES) zugunsten der IG
5/10 Studien zeigten keinen signifikant positiven Effekt zugunsten der IG
|
Primärstudien berichten keine SUEs |
Primärstudien: RCTs mit low RoB SB: 6 PB: k.a. DB: 4 AB: 4 RB: 10 OB: 10
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7 non-kritischer Dom. 8
Sensitivitäts-analysen: Keine MA
Publikations-bias: nicht addressiert |
1a |
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|
Li et al. 2014: "A systematic review on patient-reported outcomes in cancer survivors of randomised clinical trials: direction for future research."
Eingeschlossene Studien: Antoni, et al. 2009 Berry, et al. 2011, Boesen, et al. 2011 Boundouki, et al. 2004 Brown, et al. 2006 Butler, et al. 2009 Cadmus, et al. 2009 Carmack, et al. 2011 Danhauer, et al. 2009 Ell, et al. 2011 Gotay, et al. 2007 Griffith, et al. 2009 Grunfeld, et al. 2011 Hack, et al. 2007 Jones, et al. 2006 Lovell, et al. 2010 McCorkle, et al. 2009 Montgomery, et al. 2007 Mutrie, et al. 2007 Nielsen, et al. 2003 Partin, et al. 2004 Rottmann, et al. 2012 Smith, et al. 2010 Strong, et al. 2008 Syrjala, et al. 2008 Temel, et al. 2010 Thomas, et al. 2012 Thornton, et al. 2009 Tsay, et al. 2008 Velikova, et al. 2004; 2010 Vodermaier, et al. 2011 Wulff, et al. 2012
|
SysRev
Suchzeitraum: Januar 2000 – Juli 2013
Datenbanken: Wissenschaftlicher Zitationsindex erweitert PsycINFO, Medline (1950+) OvidSP CINAHL
Einschluss-Kriterien: P: erwachsene Krebspatienten I: "supportive care interventions" C: TAU/UC O: PROMs S: RCTs
33 RCTs in 34 Publikationen, N=5960 |
33 RCTs
12x Brustkrebs 3x Prostatakrebs 1x Eierstockkrebs 1x Mundkrebs 1x Lungenkrebs 2x Dickdarmkrebs 1x Magen- oder Leberkrebs 12x mehrere Krebsarten
Geschlecht: kA
Mittleres Alter: k.A
Länder: USA (19) UK (5) Dänemark (4) Kanada (3) Australien (1) Taiwan (1)
|
Inhalte: 15 x Psycho-edukation 13x "Case managment" 4x Sport- und Bewegungstherapie 1x regelm. QoL Assessment mit Feedback an Behandelnde
Dauer/Frequenz/ Länge: Einzelsitzung – 12 Monate Gruppentherapie 15min – 90min
Post-Intervention – 24 Monate Follow-Up
Kontrollgruppen: TAU/UC |
Primäre Endpunkte: Nicht aufgeschlüsselt nach Outcome
Diverse PROMs (HQoL, Distress, Schmerz, Fatigue etc.)
Verwendete Messinstrumente: divers |
1. Diverse PROMs à Psychoedukation: In 12/15 RCTs signifikante Effekte zugunsten der IG
|
Keine SUEs berichtet |
Primärstudien: Qualitäts-kiterien nach "Effective Public Health Practice Project" 5x Strong 28x moderate
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,13 non-kritischer Dom. 1,3,5,6,8,10,14
Sensitivitäts-analysen: Keine MA durchgeführt aufgrund starker Heterogenität der Interventionen
Publikations-Bias: nicht addressiert
|
1a- |
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|
Faller et al. 2013: "Effects of Psycho-Oncologic Interventions on Emotional Distress and Quality of Life in Adult Patients with Cancer: Systematic Review und Meta-Analysis."13
Eingeschlossene Primärstudien: 198 RCTs
|
MA
Suchzeitraum: May 2013
Datenbanken: CENTRAL Medline PsycInfo
Einschluss-kriterien: P: erwachsene Krebspatienten I: psychoonkologische Interventionen C: Aufmerkamkeits-Placebo, TAU/UC O: Distress, QoL, Depressivität, Angst S: RCTs
198 RCTS, N=22238 Patientinnen (218 Vergleiche in MA)
|
RCTs
Gemischte Krebsdiagnosen (80) Brustkrebs (78) Prostatakarz. (8) Gynekologisch (6) Melanom (5) Hematologischer Krebs (4) Andere (12) Nicht angegeben (5)
Geschlecht: Median 82% weiblich
Alter: Median 54 Jahre
Länder : USA (107) UK (18) Australien (12) Kanada (10) Schweden (9) Niederlande (7) Weitere (35)
|
Inhalte: Psychotherapie Einzel (55) Gruppe (42) Paar (10) Psychoedukation (19) Entspannungsverfahren (46) Einfache Informaationsgabe (23) Andere (12)
davon Einzel (119) Gruppe (66) Paar (8) Nicht angegeben (5)
Dauer/Frequenz/ Länge: 1-35 Sitzungen, Median 6 Sitzungen, Über 1-730 Tage, Median 42 Tage
Kontrollgruppen: TAU/UC Aufmerksamkeitskontrolle |
Primäre Endpunkte: 1. Distress 2. gesundheitsbezogene QoL 3. Depressivität 4. Angst |
1. Distress à Gesamteffekt Post-Intervention: 77 RCTs, N=? I2 = 73%; SMD=0.29 [0.20, 0.37, p <.001> Follow Up ≤6 Monate: 58 RCTs, N=? I2 = 56%; SMD=0.17 [0.09, 0.24, p <.001> Follow Up >6 Monate: 39 RCTs, N=? I2 = 32%; SMD=0.10 [0.04, 0.1, p =.003]
à Psychoedukation Post-Intervention: 12 RCTs, N=? I2 = 37%; SMD=0.18 [0.05, 0.30, p =.005] Follow Up ≤6 Monate: 11 RCTs, N=? I2 = 47%; SMD=0.30 [0.15, 0.45, p<.001> Follow Up >6 Monate: 7 RCTs, N=? I2 = 0%; SMD=0.11 [0.00, 0.21, p =.051]
2. QoL à Gesamteffekt Post-Intervention: 66 RCTs, N=? I2 = 78%; SMD=0.26 [0.15, 0.37, p <.001> Follow Up ≤6 Monate: 47 RCTs, N=? I2 = 65%; SMD=0.22 [0.12, 0.33, p <.001> Follow Up >6 Monate: 27 RCTs, N=? I2 = 50%; SMD=0.18 [0.07, 0.28, p <.001>
à Psychoedukation Post-Intervention: 8 RCTs, N=? I2 = 0%; SMD=0.2 [0.10, 0.30, p <.001> Follow Up ≤6 Monate: 8 RCTs, N=? I2 = 34%; SMD=0.13 [-0.01, 0.27, p=.07] Follow Up >6 Monate: 8 RCTs, N=? I2 = 54%; SMD=0.18 [0.02, 0.34, p =.029]
3. Depressivität à Gesamteffekt Post-Intervention: 72 RCTs, N=? I2 = 56.5%; SMD=0.33 [0.25, 0.41, p <.001> Follow Up ≤6 Monate: 40 RCTs, N=? I2 = 40.8%; SMD=0.2 [0.11, 0.28, p <.001> Follow Up >6 Monate: 26 RCTs, N=? I2 = 47.1%; SMD=0.14 [0.05, 0.24, p =.002]
à Psychoedukation Post-Intervention: 9 RCTs, N=? I2 = 11%; SMD=0.14 [0.03, 0.25, p =.016] Follow Up ≤6 Monate: 9 RCTs, N=? I2 = 23%; SMD=0.23 [0.11, 0.36, p<.001> Follow Up >6 Monate: 5 RCTs, N=? I2 = 52%; SMD=0.13 [-0.05, 0.3, p =.16]
4. Angst à Gesamteffekt Post-Intervention: 74 RCTs, N=? I2 = 60%; SMD=0.38 [0.29, 0.46, p <.001> Follow Up ≤6 Monate: 38 RCTs, N=? I2 = 73%; SMD=0.34 [0.2, 0.47, p <.001> Follow Up >6 Monate: 15 RCTs, N=? I2 = 33%; SMD=0.17 [0.06, 0.28, p =.003]
à Psychoedukation Post-Intervention: 7 RCTs, N=? I2 = 0%; SMD=0.22 [0.1, 0.33, p <.001> Follow Up ≤6 Monate: 7 RCTs, N=? I2 = 30%; SMD=0.24 [0.1, 0.39, p<.001> Follow Up >6 Monate: 3 RCTs, N=? I2 = 73%; SMD=0.07 [-0.08, 0.23, p =.35]
|
Nicht berichtet |
Primärstudien: RCTs mit low RoB SB: 51 PB: kA DB: kA AB: 122 RB: 141 OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2, 7, 13 non-kritischer Dom. 3, 10,
Sensitivitäts-analysen: Bei hoher Heterogenität (l²>70%) Ausschluss vjew. einer Studie aus MA & Moderatorenanalysen (u.A. Alter, Tumorart)
Weiterhin a priori geplante Subgruppenanalysen (siehe Hauptergebnisse)
Publikations-bias: Visuelle Prüfung der Funnel-Plots
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1a- |
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Psychoedukation RCTs (2015 – 2020)
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Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Patienten-merkmale |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Finanzierung / Conflict of Interest |
Methodische Bemerkungen |
Evidenzklasse |
|
Unterstützende Evidenz (7/13) |
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Li et al., 2019: Effect of a patient education and rehabilitation program on anxiety, depression and quality of life in muscle invasive bladder cancer patients treated with adjuvant chemotherapy |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=130 Post-Intervention: N=130
kA zur Analyse-Technik
Land: China 2015-2017 |
PatientInnen mit invasivem Blasenkrebs, während Chemotherapie
Geschlecht: Ca. 15.5% weiblich
Alter: Mittelwert: ca. 57,6 |
Arm A: NB=65 NP=65 Patientenedukation und Rehabilitationsprogramm (PERP), 16 Wochen, alle 2 Wochen Sitzungen, pro Sitzung ca. 30min
Arm B: NB=65 NP=65 CAU |
Erhebungszeitpunkte: Baseline Post-Intervention
Primäre Endpunkte: 1. Angst (HADS-A) 2. Depressivität (HADS-D) 3. QoL (global) (EORTC QLQ-C30) |
1. Angst à PERP versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von PERP
2. Depressivität: à PERP versus CAU: Post-Intervention: Keine sign.n Gruppenunterschiede
3. QoL (global): à PERP versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von PERP
|
Keine berichtet |
Keine Angaben zur Finanzierung
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2 low PB: high DB: high AB: low RB: unclear
Geplante Fallzahl erreicht (N=130) |
|
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Al-Sulaiman et al., 2018 : Exploring the effectiveness of crisis counseling and psychoeducation in relation to improving mental well-being, quality of life and treatment compliance of breast cancer patients in Qatar |
RCT, prospektiv, offen, monozentrisch, 3 Arme
Randomisiert: N = 201 Post-Intervention: N = kA Follow-Up : N = kA (10 Pat. "non-compliant", gleichverteilt über Gruppen)
kA zur Analyse-Technik
Land : Qatar 2012-2015 (Rekrutierung) |
Brustkrebspatientinnen, frühe Stadien (I-III)
Geschlecht : 100% weiblich
Alter : 30-50+ Mittelwert : kA |
Arm A : NR = 67 NPI = kA NFU = kA
PE, Einzel, 6x 60-90min Sitzungen über 12 Wochen
Arm B : NR = 67 NPI = kA NFU = kA
Krisenberatung (KB) one-to-one, sechs 60-90min Sessions über 12 Wochen
Arm C : NR = 67 NPI = kA NFU = kA
CAU
|
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (18 Monate)
Primäre Endpunkte: 1. Depressivität (DASS-21) 2. Ängstlichkeit (DASS-21) 3. Stress (DASS-21) 4. QoL (global) (EORTC QLQ-C30) |
1. Depressivität à PE versus KB versus CAU : Post-Intervention: Sign. Gruppenunterschiede zugunsten von PE und KB jeweils verglichen mit CAU; sign. Gruppenunterschiede zugunsten von PE verglichen mit KB
Follow-Up : Sign. Gruppenunterschiede zugunsten von PE und KB jeweils verglichen mit CAU; keine Unterschiede zwischen PE und KB
2. Ängstlichkeit: à PE versus KB versus CAU : Post-Intervention: Sign. Gruppenunterschiede zugunsten von PE und KB jeweils verglichen mit CAU ; keine Unterschiede zwischen PE und KB
Follow-Up : Sign. Gruppenunterschiede zugunsten von PE und KB jeweils verglichen mit CAU; keine Unterschiede zwischen PE und KB
3. QoL (global): à PE versus KB versus CAU : Post-intervention : Sign. Gruppenunterschiede zugunsten von PE und KB, jeweils verglichen mit CAU ; keine Unterschiede zwischen PE und KB
Follow-Up : Sign. Gruppenunterschiede zugunsten von PE und KB für Subskala emotional functioning ; keine Unterschiede zwischen PE und KB |
Nicht berichtet |
Keine Angabe zur Finanzierung
Laut Angaben keine COI
|
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: unclear RB: unclear
Keine Fallzahlplanung
„While this may be considered quite a small sample, the maximum sample size was limited by the overall number of patients in the country”
Follow-Up eigtl. für 6 Monate Post-Intervention geplant
"Another potential limitation of this study is that the assessment of the long-term effects of the crisis counseling and psychoeducation interventions was not achieved at 6 months as planned, but was delayed until 18 months after the interventions. This was because most patients were unavailable at the 6-month mark, whether due to extended travel commitments or because they simply did not respond to requests from the research assistants." |
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Aliasgharpour et al., 2018: The Effect of Pain Management Training on the Severity of Pain in Patients with Cancer: A Clinical Trial Study |
RCT, offen, prospektiv, multizentrisch, 2 Arme
Randomisiert: N=98 Post-Intervention: N= 98 Follow-Up 1: N= 98
kA zur Analyse-Technik, aber auch keine fehlenden Werte
Land: Iran 2014 |
Krebspatienten mit Schmerzscore über 4 auf VAS
Geschlecht: 49,9% weiblich
Alter: 18-66 Mittelwert: |
Arm A: NB=49 NP= 49 NFU1= 49 6 Edukations-Sitzungen (ES) und ein Trainingsmanual, über 3 Wochen, 20min pro Sitzung
Arm B: NB=49 NP= 49 NFU1= 49 CAU
|
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up 1 (3 Wochen)
Primäre Endpunkte: 1. Schmerz (VAS) |
1. Schmerz à ES versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von ES
Follow-Up 1: Sign. Gruppenunterschiede zugunsten von ES
|
Keine berichtet |
Tehran University of Medical Sciences, Tehran, Iran
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2 unclear PB: high DB: high AB: low RB: unclear
Geplante Fallzahl erreicht (N=49 pro Gruppe) |
|
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Mohd-Sidik (2018): Effectiveness of chemotherapy counselling on self-esteem and psychological affects among cancer patients in Malaysia: Randomized controlled trial. |
RCT prospektiv, multizentrisch, offen, 2 Arme
Randomisiert : N = 2140 Follow-Up 1: N = 2128 Follow-Up 2: N = 2126 Follow-Up 3: N = 2120
PP-Analyse Ausgewertet: N = 2120
Land: Malaysia 2016-2017 |
Krebs-patienten (alle Typen & Stadien)
Geschlecht: 56.7% weiblich
Alter: <45: 12,5% 45-54: 16.9% 66-64: 31.8% >65: 48.7%
|
Arm A: EG NB = 1070 N FU1= 1065 NFU2= 1063 NFU3= 1060
Edukationsmodul zur Begleitung der Chemotherapie-Zyklen, je einmal zu Baseline, FU, FU2 und FU3 insg. 4x 45-60 Min
Arm B: TAU NB = 1070 NFU1 = 1063 NFU2= 1063 NFU3= 1060
|
Erhebungszeitpunkte: Baseline Follow-Up 1 (3-6 Wochen) Follow-Up 2 (6-12Wochen) Follow-Up 3 (12-18 Wochen)
Jeweils VOR Durchführung der Edukation
Primäre Endpunkte: 1. Angst (Häufigkeit) 2. Depressivität (Häufigkeit)
Sekundäre Endpunkte: 1. Selbstwert (RSES) |
1. Angst à EG vs. TAU Sign. reduzierte Häufigkeit von Angst nach der 1., 2. und 3. Sitzung zugunsten der EG
2. Depressivität à EG vs. TAU Sign. reduzierte Häufigkeit von Depression nach der 1., 2. Und 3. Sitzung zugunsten der EG |
Nicht berichtet |
Geran Universiti Putra Malaysia
Laut Angaben kein COI |
Risk of Bias
SB1: low SB2 low PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N=2140) nicht erreicht |
|
|
Wu et al., 2018: Effects of a Psychoeducational Intervention in Patients With Breast Cancer Undergoing Chemotherapy |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=40
kA zu Analyse-Technik Ausgewertet: N=40
Land: Taiwan |
Brustkrebspatientinnen, während Chemotherapie (insgesamt 6 Zyklen über 18 Wochen), Stage I-IV,
Geschlecht: 100% weiblich
Alter: 30-76 Mittelwert: 51,2 |
Arm A: NB=20 (kA zu weiteren MZP) PE, 6 x 60-minütige face-to-face Sitzungen während 5 Chemotherapie-Zyklen
Arm B: NB=20 (kA zu weiteren MZP) CAU |
Erhebungszeitpunkte: Baseline (T1), während des 3. (T2) und 5. (T3) Chemozyklus, Post-Intervention (2 Wochen nach letzten Zyklus, T4)
Primäre Endpunkte: 1. Angst (HADS-A) 2. Depressivität (HADS-D) 3. Krankheitsspezifisches Wissen über Selbstfürsorge 4. QoL (EORTC QLQ-C30, EORTC QLQ-BR23) 5. Selbstwirksamkeit 6. Resilienz
|
1. Angst à PE versus CAU Post-Intervention: Sign. Gruppenunterschiede zugunsten von PE
2. Depressivität: à PE versus CAU Post-Intervention: Sign. Gruppenunterschiede zugunsten von PE
3. QoL – Global QoL: à PE versus CAU Post-Intervention: Sign. Gruppenunterschiede zugunsten von PE |
Nicht berichtet |
Keine Angaben zur Finanzierung
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2 unclear PB: high DB: high AB: low RB: unclear
Geplante Fallzahl erreicht (N = 20 pro Gruppe)
Sign. verschiedene Verteilung von Krebsstadien zwischen den Gruppen
Sign. höherer global health status (QLQ-C30) in PE (EG) bei Baseline |
|
|
Li et al., 2017: Psychological intervention improves life quality of patients with laryngeal cancer |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=210 Post-Intervention N= 210
kA zur Analyse-Technik
Land: China 2014-2016 |
Kehlkopfkrebs-Patienten, bevorstehende OP
Geschlecht: 42,38% weiblich
Alter: 39-76 Mittelwert: 55,26 |
Arm A: NB=102 NP=102 PE, vor, während und nach OP
Arm B: NB=108 NP=108 CAU |
Erhebungszeitpunkte: Baseline (1 Woche Prä-Intervention) Post-OP (3 Monate)
Primäre Endpunkte: 1. Depressivität (HAMD) 2. Angst (HAMA) 3. QoL (global) (EORTC QLQ-C30) |
1. Depressivität à PE versus CAU: Post-OP: Sign. gruppenunterschiede zugunsten von PE
2. Angst: à PE versus CAU: Post-OP: Sign. Gruppenunterschiede zugunsten von PE
3. QoL(global): à PE versus CAU: Post-OP: Sign. Verbesserungen nur in PE, nicht in CAU
|
Keine berichtet |
The Second Affiliated Hospital of Xi’an Jiaotong University and Shaan’xi Province Government
Laut Angaben keine COI
|
Risk of Bias
SB1: unclear SB2 unclear PB: high DB: high AB: low RB: unclear
Bei QoL kein Gruppenvergleich berichtet
Keine Fallzahlplanung |
|
|
Ohlsson-Nevo et al., 2016: Effects of a psycho-educational programme on health-related quality of life in patients treated for colorectal and anal cancer: A feasibility trial |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 86 Post-Intervention: N = 80 Follow-Up 1: N = 71 Follow-Up 2: N = 66
ITT-Ansatz, ohne Imputation
Land: Schweden 2007-2010 |
Anal- (ca. 2,4%) und Darmkrebspatienten (Rest). Operative Behandlung
Geschlecht: ca. 37,24% weiblich
Alter: Mittelwert: 66 |
Arm A: NB = 47 NP = 44 NFU1 = 43 NFU2 = 38 PE-Programm (PEP), Vorträge + anschließende Diskussion, Gruppe, wöchentlich, 7x120min,
Arm B: NB = 39 NP = 36 NFU1 = 28 NFU2 = 28 CAU
|
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up 1 (5 Monate) Follow-Up 2 (11 Monate)
Primäre Endpunkte: QoL (SF-36, aufgeteilt in overall mental health status (MCS) und overall physical health status (PCS)) |
1. QoL – mental health à PEP versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von PEP (d= 0.51)
Follow-Up 1: Keine sign. Gruppenunterschiede
Follow-Up 2: Keine sign. Gruppenunterschiede
2. QoL – physical health: à PEP versus CAU: Post-Intervention: Keine sign. Gruppenunterschiede
Follow-Up 1: Keine sign. Gruppenunterschiede
Follow-Up 2: Keine sign. Gruppenunterschiede
|
Nicht berichtet |
Research Committee of Örebro County Council
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2 unclear PB: high DB: high AB: unclear RB: unclear
Machbarkeits-Studie
kA zu Fallzahlplanung
PEP-Gruppe sign. höhere Werte auf Subskalen general Health und Social Functioning zu Baseline
|
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Keine Hinweise für höhere Wirksamkeit des Treatments (6/13) |
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Chow et al., 2020: A theory‐driven psycho‐educational intervention programme for gynaecological cancer patients during treatment trajectory: A randomised controlled trial |
RCT, prospektiv, multizentrisch, verblindet (Proband*innen), 2 Arme
Randomisiert: N=202 Post-Intervention: N=191
ITT-Ansatz, kA zu Imputationsmethode Ausgewertet: N=191
Land: China (Hong-Kong) 2016-2018 |
Gynäkologische Krebspatientinnen, neu diagnostiziert (Diagnose innerhalb der letzten 3 Monate)
Geschlecht: 100% weiblich
Alter: Mittelwert: 54,6 |
Arm A: NB=102 NP=94 PE, 4 Sitzungen über 12 Wochen, 3 face-to-face-Sitzungen von 45-60min, ein Telefongespräch von 20-35min; Zeitpunkt der Sitzungen individuell wählbar/angepasst
Arm B: NB=100 NP=98 WL/AC
|
Erhebungszeitpunkte: Baseline Post-Intervention
Primäre Endpunkte: 1. Unsicherheit (MUIS) 2. Angst (HADS-A) 3. Sexuelle Funktion (SVQ) |
1. Angst: à PE versus AC: Post-Intervention: Keine sign. Gruppenunterschiede, sign. Zeiteffekt à Verbesserungen in beiden Gruppen
2. Sexuelle Funktion: à PE versus AC: Post-Intervention: Frauen in PE sexuell aktiver und höhere Einschätzung, dass Partner sexuell an ihnen interessiert ist verglichen zu AC; sign. Gruppenunterschiede auf Subskala Intimität zugunsten von PE
|
Nicht berichtet |
Health and Medical Research Fund
Laut Angaben keine COI |
Risk of Bias
SB1: unclear SB2 unclear PB: high DB: high AB: low RB: unclear
Geplante Fallzahl erreicht (N = 202)
Baseline-Ängstlichkeit in PE-Gruppe leicht erhöht verglichen zur AC-Gruppe
Sexuelle Funktion zu Baseline wurde nicht erhoben |
|
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Li et al., 2018: Effect of one comprehensive education course to lower anxiety and depression among Chinese breast cancer patients during the postoperative radiotherapy period - one randomized clinical trial
|
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=290 Post-Intervention: N=281
PP-Analyse Ausgewertet: s.o.
Land: China 2013-2015 |
Brustkrebspatientinnen (einseitig), während postoperativer Bestrahlungsperiode, Stage I-IV
Geschlecht: 100% weiblich
Alter: 25-67 Mittelwert: 46,2 |
Arm A: EG NB=145 NP=136 PE und Management-Fertigkeiten, 1x3h Sitzung
Arm B: NB=145 NP=145 CAU |
Erhebungszeitpunkte: Baseline Post-Intervention (nach Radiotherapie)
Primäre Endpunkte: 1. Depressivität (HADS-D) 2. Angst (HADS-A) |
1. Depressivität è EG vs. CAU Post-Intervention: Keine sign. Gruppenunterschiede
2. Angst è EG vs. CAU Post-Intervention: Keine sign. Gruppenunterschiede |
Nicht berichtet |
Keine Angaben zur Finanzierung
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2 unclear PB: high DB: high AB: high RB: unclear
Geplante Fallzahl erreicht (N = 242) |
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Yang et al., 2018: Pilot Randomized Phase II Trial of the Enhancing Quality of Life in Patients (EQUIP) Intervention for Patients With Advanced Lung Cancer |
RCT, offen, prospektiv, monozentrisch, 2 Arme
Randomisiert: N=69 Post-Intervention: N=58
kA zur Auswertungs-Methode
Ausgewertet: N=58
Land: Singapur
|
Fortgeschrittener Lungenkrebs, neue Diagnose (max. 8 Wochen her)
Geschlecht: ca. 68% weiblich
Alter: Mittelwert: ca. 58,8 |
Arm A: NB=35 NP=28 Enhancing Quality of Life in Patients (EQUIP) Intervention, 4 edukative face-to-face Sitzungen
Arm B: NB=34 NP=30 CAU |
Erhebungszeitpunkte: Baseline Post-Intervention
Primäre Endpunkte: 1. QoL (FACT-L) 2. Lungenkrebs-Symptome (LCS) 3. Trial Outcome Index (TOI)
Sekundäre Endpunkte: 1. Depressivität (HADS-D) Angst (HADS-A) |
Post-Intervention: Keine sign. Gruppenunterschiede auf relevanten Endpunkten, keine klinisch bedeutsame Verbesserung in EQUIP |
Nicht berichtet |
National Cancer Centre Research Fund
Laut Angaben keine COI |
Risk of Bias
SB1: unclear SB2 unclear PB: high DB: high AB: unclear RB: unclear
Vielleicht Selektionsbias
Phase-2-Pilotstudie
Geplante Fallzahlplanung erreicht (N = 69) |
|
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Bourmaud et al., 2017: Cancer-related fatigue management: evaluation of a patient education program with a large-scale randomised controlled trial, the PEPs fatigue study |
RCT, prospektiv, offen, multizentrisch, 2 Arme
Randomisiert: N = 212
Modifizierter ITT-Ansatz (Patienten mit VAS-Score von Baseline und Post-Intervention für primäres Outcome analysiert, auch wenn Intervention nicht vollst. durchlaufen)
Land: Frankreich
|
Krebspatienten (58,5% Brust, Rest andere)
Geschlecht: 84,4% weiblich
Alter: Mittelwert: 55,9 |
Arm A: NB=106 NP=66 (gesamte Intervention absolviert) Edukationsprogramm für Fatigue (PEPS): Gruppenintervention, 5 x 2h-Sitzungen über 6 Wochen
Arm B: NB=106 NP= 81 CAU
|
Erhebungszeitpunkte: Baseline Post-Intervention
Primäre Endpunkte: 1. Fatigue (VAS)
Sekundäre Endpunkte: 1. Fatigue (FACT-F, R-PFS) 2. QoL (global) (QLQ-C30) 3. Angst (HADS-A) 4. Depressivität (HADS-D)
|
1. Fatigue à PEPS versus CAU Post-Intervention: Keine sign. Gruppenunterschiede
2. QoL (global) à PEPS versus CAU Post-Intervention: Keine sign. Gruppenunterschiede
3. Angst: à PEPS versus CAU Post-Intervention: Keine sign. Gruppenunterschiede
4. Depressivität à PEPS versus CAU Post-Intervention: Keine sign. Gruppenunterschiede
|
keine |
French Ministry of Health (PHRC 2006 [Hospital Program of Clinical Research])
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2 unclear PB: high DB: high AB: unclear RB: unclear
Geplante Fallzahl erreicht (N = 80 pro Gruppe) |
|
|
Chan et al., 2017: A culturally adapted survivorship programme for Asian early stage breast cancer patients in Singapore: A randomized, controlled trial |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 88
ITT-Ansatz Ausgewertet: N = 72
Land: Singapur 2015-2016 |
Brustkrebspatientinnen in frühen Stadien (Stage I-III), abgeschlossene Chemotherapie
Geschlecht: 100% weiblich
Alter: Mittelwert: 50,3 |
Arm A: NB = 43 NP = 34 PE in der Gruppe (PEG), 3 Wochen, wöchentlich, 3x4,5h
Arm B: NB = 45 NP = 38 CAU |
Erhebungszeitpunkte: Baseline Post-Intervention (während 2 Monaten nach Intervention)
Primäre Endpunkte: 1. Distress (RSCL)
Sekundäre Endpunkte: 1. QoL (global) (EORTC QLQ-C30) 2. Angst (BAI) 3. Zufriedenheit (Satisfaction Questionnaire)
|
1. Distress: à PEG versus CAU: Post-Intervention: Keine sign. Gruppenunterschiede; Verbesserungen in beiden Gruppen
2. QoL(global): à PEG versus CAU: Post-Intervention: Keine sign. Gruppenunterschiede
3. Angst: è PEG versus CAU: Post-Intervention Keine sign. Gruppenunterschiede, Verbesserungen in beiden Gruppen
|
Nicht berichtet |
National Cancer Centre Community Cancer Fund Grant Call, Pretty in Pink 2014 event
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2 unclear PB: high DB: high AB: high RB: unclear
Geplante Fallzahl nicht erreicht (N = 80)
Phase 2-Studie |
|
|
Riese et al., 2017: Effectiveness of a standardized patient education program on therapy-related side effects and unplanned therapy interruptions in oral cancer therapy: a cluster-randomized controlled trial |
RCT (cluster-randomisiert), prospektiv, multizentrisch, offen, 2 Arme
Randomisiert: N=165 Post-Intervention: N=161 Follow-Up 1: N=145 Follow-Up 2: N=130 Follow-Up 3: N=98
PP-Ansatz Ausgewertet: s.o.
Land: Deutschland 2014 |
Krebspatienten (Darm 15,5%, Knochenmark 12,7%, Brust 10%, Lunge 8,06%)
Geschlecht: 53,93% weiblich
Alter: Mittelwert: ca. 70 Jahre |
Arm A: NB=111 NP=107 NFU1=97 NFU2=84 NFU3=58 Patienten-Edukations-programm (PEP), 5 face-to-face Einzelsitzungen, Sitzung 2 und 3 alle zwei Wochen, Sitzung 3 und 4 monatlich, ca. 30-45min
Arm B: NB=54 NP=48 NFU1=46 NFU2=40 NFU3=40 CAU
|
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up 1 (2 Wochen) Follow-Up 2 (6 Wochen) Follow-Up 3 (10 Wochen)
Primäre Endpunkte: 1. Häufigkeit von therapiebezogenen Nebenwirkungen 2. Häufigkeit von ungeplanten Therapieunterbrechungen
|
1. Schmerzen à PEP versus CAU: Keine sign. Gruppenunterschiede
2. Übelkeit à PEP versus CAU: Keine sign. Gruppenunterschiede
3. Fatigue à PEP versus CAU: Keine sign. Gruppenunterschiede
|
Nicht berichtet |
German Federal Ministry of Health within the National Cancer Plan
Laut Angaben keine COI |
Risk of Bias
SB1: unclear SB2 unclear PB: high DB: high AB: high RB: unclear
Geplante Fallzahl nicht erreicht (N = 210) |
|
Psychoonkologische E-Health Interventionen
|
Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Merkmale untersuchter Studien |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Methodische Bemerkungen |
Evidenzklasse |
|
Larson et al. 2020: "The effect of telehealth interventions on quality of life of cancer survivors: A systematic review and meta-analysis."1
Eingeschlossene Primärstudien: Ashing 2016 David 2011 Forbes 2015 Freeman 2015 Galiano-Castillo 2016 Hawkes 2014 Kim 2011 Malmström 2016 Nelson 2008 Van der Berg 2015 Williams 2017 |
MA
Suchzeitraum: Bis 31. Oktober 2017
Datenbanken: PubMed CINHAL Ebsco Health (Medline complete)
Einschluss-kriterien: P: Erwachsene Krebspatienten nach abgeschl. Erstbehandlung ("Cancer Survivors") I: telehealth/tele-medicine C: TAU/UC O: overall QoL S: RCTs
11 RCTS, N=1349 Patienten
|
RCTs
Cancer Survivors (Brust 6, Gemischt 2, Oesophagus-karzinom 1, Zervixkarzinom1, Colo-Rektalkarzinom 1)
Geschlecht: 75% weiblich
Mittleres Alter: 46 – 66
Länder : Australien USA Deutschland Niederlande Kanada Südkorea Spanien Schweden |
Inhalte: 3 x web-basiertes Selbstmanagement 5 x telefon-basiert 1 x mail-basierte Beratung 1 x Video-Konferenz 1 x internet-basierte Tele-Rehabilitation
Frequenz: Mehrheitlich wöchentlich; bei Selbstmanagement frei wählbar
Dauer: 2 – 12 Monate
Kontrollgruppen: Keine genaueren Angaben, TAU/UC |
Primäre Endpunkte: 1. QoL
Verwendete Messinstrumente: QoL EORTC QLQ-C30 FACT-B FACT-G FACT-C FACT-Cx
|
1. QoL àGesamteffekt: Post-Intervention: 11 RCTs, N=1349, I2 = 95%; SMD=0.75 [0.20, 1.30, p = .007] Fail-safe-N: 202 Random-Effects Model
àNach Entfernung von Ausreißern: Post-Intervention: 9 RCTs, N=1163, I2 = 0%; SMD=0.14 [0.03, 0.26, p = .016] Random-Effects Model Fail-safe-N: 11 Ausreißer: Nelson 2008 (telefon-basiert), Van der Berg 2015 (web-basiertes Selbstmanagement)
àTelefon versus TAU/UC Post-Intervention: 5 RCTs, SMD=0.70 [0.02, 1.39, p=.04]
|
Keine SUEs berichtet
RCTs berichten UEs nicht |
Primärstudien: PEDro Skala, range 6-8 von 11; Risiko für DB und PB hoch, keine Verblindung. Risiko für SB hoch, keine verblindete Gruppenzuordnung
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,9,13 non-kritischer Dom. 1,3,5,6,8,11,12,
Sensitivitäts-analysen: Siehe Ergebnisse nach Entfernung von Ausreißern
Publikations-bias: Funnel-Plot Analyse; Fail-safe N; |
1a- |
|
Xu et al. 2019: "Effectiveness of e‐health based self‐management to improve cancer‐related fatigue, self‐efficacy and quality of life in cancer patients: Systematic review and meta‐analysis"2
Eingeschlossene Primärstudien: Admiraal 2017 Bantum 2014 Boele 2018 Foster 2016 Golsteijn 2018 Lee 2014 Owen 2005 Smith 2018 Somers 2018 Syrjala 2018 Vallerand 2018 van den Berg 2015 Willems 2017 Zhang 2013 Zhu 2018 |
MA
Suchzeitraum: Bis 14. Juli 2019
Datenbanken: CENTRAL PubMed CINHAL Embase Web of Science
Einschluss-kriterien: P: Erwachsene Krebspatienten I: e-Health (app, website, mail, telephone) C: nicht e-Health basiert O: Fatigue, Selstwirksamkeits-erleben, QoL S: RCTs
15 RCTS (13 in MA), N=2337 Patienten
|
RCTs
Erwachsene Krebspatienten versch Tumorstadien (Brust 6, Gemischt 4, Hämatologischer Krebs 2, Gliome 1, Rektalkarzinom 1)
Geschlecht: kA
Mittleres Alter: 41,5 – 66,6
Länder : USA Niederlande UK Kanada China Südkorea |
Inhalte: Behaviour change Medical management Psychological management (Depression therapy, CST, Psychoeducation, psychological support)
12 x web-basiert 2 x telefon-basiert 1 x App
Länge & Frequenz: Int. meist modular aufgebaut, Zugang für 4 Wochen – 6 Monate, Bis zu 5 wöchentliche Einheiten
Kontrollgruppen: 6x Warteliste 5x TAU/UC 2x Info-Broschüre 2x Face-to-Face-Beratung |
Primäre Endpunkte: 1. Fatigue 2. Selbstwirk-samkeits-erleben 3. QoL
Verwendete Messinstrumente: Fatigue FSI FACT-F FACIT-F CIS BFI PROMIS
QoL EORTC QLQ-C30 FACT-B FACT-G
|
1. Fatigue àGesamteffekt: Post-Intervention: 9 RCTs, N=1734, I2 = 54%; SMD=−0.24 [−0.39, −0.08, p = .03] GRADE: very low
àIG versus TAU/UC Post-Intervention: 7 RCTs, N=1524, I2 = 23%; SMD=−0.30 [−0.42, −0.17, p < .01] GRADE: moderate
àIG versus other support Post-Intervention: 2 RCTs, N=210, I2 = 0%; SMD=0.18 [−0.09, 0.45, p=.18] GRADE: low àkeine signifikanten Subgruppenunter-schiede zwischen telefon-basiert versus web-basiert
2. QoL àGesamteffekt: Post-Intervention: 7 RCTs, N=1502, I2 = 29%; SMD=0.09 [−0.04, 0.22, p = .18] GRADE: low
àIG versus TAU/UC Post-Intervention: 5 RCTs, N=1218, I2 = 29%; SMD=0.14 ([0.00, 0.29, p=.23] GRADE: moderate
àIG versus other support Post-Intervention: 2 RCTs, N=284, I2 = 0%; SMD=0.09 [-0.32, 0.14, p=.54] GRADE: low àkeine signifikanten Subgruppenunter-schiede zwischen telefon-basiert versus web-basiert
|
Keine SUEs berichtet
RCTs berichten UEs nicht |
Primärstudien: RCTs mit low RoB SB: 7 PB: 0 DB: 1 AB: 14 RB: 4 OB: 14
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7,11,15 non-kritischer Dom. 1,3
Sensitivitäts-analysen: Effekte robust gegenüber Entfernung jeweils einer Studie
Publikations-bias: "publication bias was not evaluated because fewer than 10 studies were included." (p. 3436) |
1a- |
|
Zhang et al. 2018: "Effectiveness of telephone‐based interventions on health‐related quality of life and prognostic outcomes in breast cancer patients and survivors—A meta‐analysis"3
Eingeschlossene Primärstudien: Wyatt 2004 Kimman 2011 Heiney 2003 Park 2012 Badger 2005 Ligibel 2012 Salonen 2014 Sandgren 2007 Zhu 2015 Craddock 1999 Braden 1998 Allard 2007 Allan 2002 Mishel 2005 |
MA
Suchzeitraum: Bis Mai 2015
Datenbanken: CENTRAL Web of science Medline EMBASE CNKI CBM Einschluss-kriterien: P: Brustkrebs-patientinnen I: telefon-basiert C: nicht telefon-basiert O: / S: RCTs
14 RCTS, N=2002 Patienten
Studien ohne ausreichende quantitative Daten wurden exkludiert
|
RCTs
Mamma-Ca
Geschlecht: 100% weiblich
Mittleres Alter: 44 – 64
Länder : USA Niederlande Finnland Kanada China
|
Inhalte: Telephone interview of home nursing telephone-based physical activity intervention health education or emotional expression intervention selfcare telephone contact symptoms management guided use of audiotaped cognitive-behavioural strategies
Frequenz: 1 x monatlich – 6 x wöchentlich
Dauer: 3 Wochen – 13 Monate
Kontrollgruppen: 6 x keine Intervention 8 x TAU/UC |
Primäre Endpunkte: 1. QoL 2. Physiologisches Funktionsniveau 3. Häusliches Funktionsniveau 4. Selbstwirk-samkeits-erleben 5. Angst 6. Depressivität 7. Fatigue
Verwendete Messinstrumente: QoL EORTC QLQ-C30 QoL-BC FACT-B SF-36
Angst POMS STAI
Depressivität POMS
Fatigue QoL-BC MFI FACIT-F
|
1. QoL àGesamteffekt: Post-Intervention: 7 RCTs, N=973, I2 = 91%; SMD=0.54 [0.08, 1.00, p = .02] Random-effects-model
2. Angst àGesamteffekt: Post-Intervention: 5 RCTs, N=726, I2 = 45%; SMD=–0.16 [–0.30, –0.01, p = .04] Fixed-effects model
3. Depressivität àGesamteffekt: Post-Intervention: 7 RCTs, N=239, I2 = 40%; SMD=–0.14 [–0.40, 0.11, p = .28] Fixed-effects model
4. Fatigue àGesamteffekt: Post-Intervention: 4 RCTs, N=339, I2 = 90%; SMD=–0.7 [–1.43, 0.03, p = .06] Random-effects model 3. |
Keine SUEs berichtet
RCTs berichten UEs nicht |
Primärstudien: RCTs mit low RoB SB: 5 PB: 2 DB: 2 AB: 14 RB: 14 OB: nicht berichtet
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,13,15 non-kritischer Dom. 1,10,12
Sensitivitäts-analysen: Nicht durchgeführt
Publikationsbias: nicht geprüft |
1a- |
|
Chen et al. 2018: "Effect of telehealth intervention on breast cancer patients' quality of life and psychological outcomes: A meta-analysis."4
Eingeschlossene Primärstudien: Allard 2007 Ashing 2016 Ashin 2014 Beaver 2009 Berg 2015 Carpenter 2014 Chee 2016 Chen 2015 Damholdt 2016 David 2011 Freeman 2015 Galiano-Castillo 2016 Kimman 2011 Liu 2015 Owen 2005 Ozkan 2014 Ryhanen 2013 Sandgren 2007 Winzelberg 2003 Xie 2011 |
MA
Suchzeitraum: Bis 3. Oktober 2016
Datenbanken: CENTRAL Web of science Pubmed EMBASE CNKI Einschluss-kriterien: P: diagnostizierte Brustkrebs-patientinnen I: telefon und internet-basiert C: UC O: QoL, depression, anxiety, distress, self-efficacy, percieved stress S: RCTs
20 RCTS, N=2190 Patienten
Studien ohne ausreichende quantitative Daten wurden exkludiert
|
RCTs
Mamma-Ca
Geschlecht: 100% weiblich
Mittleres Alter: 35 – 64
Länder : China Dänemark Deutschland UK Finnland Kanada Niederlande USA Spanien Türkei
|
Inhalte: u.A. Telephone based (psycho-) educational intervention, Internet support group, Online stress management, Web-based cognitive Training, Psychosocial counselling for breast cancer patients via web-based
Frequenz: Keine Angaben
Dauer: 2 Wochen – 24 Monate
Kontrollgruppen: Keine genaueren Angaben |
Primäre Endpunkte: 1. QoL 2. Depressivität 3. Angst 4. Distress 5. Selbstwirk-samkeits-erleben 6. Erlebter Stress
Verwendete Messinstrumente: QoL EORTC QLQ-C30 QoL-BC FACT-B FACT-G SF-36
Angst HAMA STAI SCL-92
Depressivität POMS CES-D BDI HAMD
Distress IES BSI-GSI |
1. QoL àGesamteffekt: Post-Intervention: 13 RCTs, N=1252, I2 = 92%; SMD=0.60 [0.18, 1.01, p = .005] Random-effects-model
àTelefon vs. UC Post-Intervention: 3 RCTs, I2 = 52%; SMD=0.14 [–0.17, 0.45, p = .39]
àTelefon+Internet vs. UC Post-Intervention: 2 RCTs, I2 = 0%; SMD=1.20 [0.80, 1.60, p < .001]
2. Depressivität àGesamteffekt: Post-Intervention: 6 RCTs, N=572, I2 = 96%; SMD=–1.29 [–2.28, –0.30, p= .01] Random-effects model
àTelefon vs. UC Post-Intervention: 2 RCTs, I2 = 99%; SMD=–10.95 [–33.27, 11.37, p= .34]
àTelefon+Internet vs. UC Post-Intervention: 2 RCTs, I2 = 85%; SMD=–0.62 [–1.60, 0.37, p= 0.22]
3. Angst àGesamteffekt: Post-Intervention: 6 RCTs, N=906, I2 = 12%; SMD=–0.09 [–0.22, 0.04, p = .17] Fixed-effects model
4. Distress àGesamteffekt: Post-Intervention: 7 RCTs, N=695, I2 = 0%; SMD=–0.25 [–0.40, –0.10, p = .001] Fixed-effects model
|
Keine SUEs berichtet
RCTs berichten UEs nicht |
Primärstudien: im Anhang; lässt sich per Link nicht öffnen;
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7 non-kritischer Dom. 3,8,10
Sensitivitäts-analysen: Effekte in QoL, Angst und Distress robust gegenüber Entfernung jeweils einer Studie; Gesamteffekt in Depressivität nicht-signifikant nach Entfernung von Ozkan 2014 (I2 = 96%; SMD=–0.57, 95% [–1.21, 0.07, p=0.08])
Publikations-bias: Begg's und Egger's-test bei Meta-Analysen mit n>=10 Studien; keine Hinweise auf Publikations-bias. |
1a- |
|
Okuyama et al. 2015: "Psychosocial telephone interventions for patients with cancer and survivors: a systematic review."5
Eingeschlossene Primärstudien: Allard 2007 Ashing-Giwa 2008 Badger 2007 Badger 2011 Badger 2012 Bailey 2004 Crane-Okada 2012 Downe-Wamboldt 2007 Gotay 2007 Heiney 2003 Hoyer 2011 Livingston 2010 Marcus 2010 Mishel 2002 Mishel 2005 Nelson 2008 Samarel 2002 Sandgren 2000 Sandgren 2007 Sheman 2012
|
SysRev
Suchzeitraum: 1966 – März 2013
Datenbanken: CENTRAL Web of science Pubmed EMBASE CNKI Einschluss-kriterien: P: erwachsene Krebspatienten I: ausschl. telefon-basierte psychosoziale Beratung C: TAU/UC, AC, andere psychosoziale Interventionen O: HRQoL S: RCTs
20 RCTS, N=3848 Patienten
Studien ohne Beratungsinhalte oder genaue Interventionsbe-schreibung wurden exkludiert
|
RCTs
Erwachsene Krebspatienten versch Tumorstadien (Brust 13, Prostata 3, Zervikaxkarzinom 2, Gemischt 2)
Geschlecht: kA
Mittleres Alter: 49 - 75
Länder : kA |
Mehrzahl (n=18) der Interventionen theoriebasiert oder mit spez. Technik (bspw. CBT); mehrheitlich Pflegepersonal (n=11)
Frequenz: Meist wöchentlich
Dauer: 2 – 20 Anrufe; Gesamtdauer zw. 65 und 720min über 2 Wochen bis zu 13 Monaten
Kontrollgruppen: Nicht genauer spezifiziert; TAU/UC |
Primäre Endpunkte: 1. QoL
Sekundäre Endpunkte: 1. Stimmung 2. Depressivität 3. Angst 4. Soziale Unterstützung 5. Stress 6. Distress 7. Körperliche und mentale Gesundheit 8. Psych. Wachstum 9. Psychosoziale Anpassung 10. Rezidivangst 11. Ressourcen-nutzung
Verwendete Messinstrumente: QoL FACT-G, QoL-CS, QoL-BC, CARES-SF, EORTC QOL-C30, QoL-BR23
Depressivität CES-D HADS
Angst STAI HADS
Distress IES
|
Signifikante Effekte auf mindestens einem erhobenen psychosozialen Endpunkt in 8/20 Studien direkt Post-Intervention;
Davon 4 Studien mit weiteren Follow-Up Erhebungen; 1 mit signifikantem Effekt
"No commonalities were identified for the nine studies with significant findings." (p.860) |
Keine SUEs berichtet
|
Primärstudien: RCTs nach CONSORT evaluiert, keine detaillierten Angaben zu Primärstudien "Also complicating this review […], is the lack of consistency in adhering to the CONSORT reporting guidelines for intervention trials" (p.867)
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,13 non-kritischer Dom. 3,10,14
Publikationsbias: nicht geprüft |
1a- |
Psychoonkologische E-Health Interventionen RCTs (2015 – 2020)
|
Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Patienten-merkmale |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Finanzierung / Conflict of Interest |
Methodische Bemerkungen |
Evidenzklasse |
||||||||||||||
|
Unterstützende Evidenz (13/28) |
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|
Borosund et al., 2020: Results from a randomized controlled trial testing StressProffen; an application-based stress-management intervention for cancer survivors |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=175 Post-Intervention: N=149
ITT-Ansatz ohne Imputation; ausgewertet: N=149
Land: Norwegen |
Krebsüberlebende/Krebspatienten, max. 1 Jahr Post-Treatment oder laufende Behandlung, alle Stages (48% Brustkrebs, 8% Gehirntumor, 6% Prostatakrebs, 5% Lymphom, 5% (Dick-)Darmkrebs, 29% andere),
Geschlecht: 82% weiblich
Alter: 20-78 Mittelwert: 52 |
Arm A: NR=84 Nm=72 StressProffen, app-basierte Stressmanagement-Intervention, 3 Monate, eine face-to-face-Einführungs-Session (Einzel oder in der Gruppe), 10 app-basierte KVT-Stressmanagementmodule, Follow-Up-Telefonate (Woche 2-3, 6-7)
Arm B: NR=88 Nm=77 CAU |
Erhebungszeitpunkte Baseline Post-Intervention
Primäre Endpunkte: 1. Distress (PSS)
Sekundäre Endpunkte: 2. Angst (HADS-A) 3. Depressivität (HADS-D) 4. QoL ( RAND-36) |
1. Distress à StressProffen versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von StressProffen (d=–0.19)
2. Angst: à StressProffen versus CAU: Post-Intervention: Keine sign. Gruppenunterschiede
3. Depressivität: à StressProffen versus CAU: Post-Intervention: Keine sign. Gruppenunterschiede
4. QoL: à StressProffen versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von Stressproffen in den Bereichen Role Physical (d=0.20), Social Functioning (d=0.17), Role Emotional (d=0.20), Mental Health (d=0.21)
|
Arm A : StressProffen SUEs : 11/84 UEs : 1/84
Arm B : CAU SUEs : 11/88 UEs : 0/88
|
The Norwegian Cancer Society (# 4602492-2013); Department of Digital Health Research at the Oslo University Hospital, Oslo, Norway
COI: Dr Clark is a consultant for Roche Diabetes Care GmbH. No other authors made any disclosures |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: high
Keine Fallzahlplanung |
|
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|
Dieng et al., 2020: Benefits of a brief psychological intervention targeting fear of cancer recurrence in people at high risk of developing another melanoma: 12-month follow-up results of a randomized controlled trial
UND
Dieng et al., 2016: Psychoeducational Intervention to Reduce Fear of Cancer Recurrence in People at High Risk of Developing Another Primary Melanoma: Results of a Randomized Controlled Trial |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=164 Follow-Up1: N=143 Follow-Up2: N=151 Follow-Up3: N=142
ITT-Ansatz mit multipler Imputation; Ausgewertet: N=151
Land: Australien Feb.-Dez. 2014
|
Krebsüberlebende (Melanom, Stage I-III) mit hohem Risiko, ein weiteres Melanom zu entwickeln
Geschlecht: 44,8% weiblich
Alter: Mittelwert: 58,5 |
Arm A: NB=80 NFU1=67 NFU2=70 NFU3=68 PE, 76 Seiten + 3 Telefongespräche mit Psychologen (individuell je nach PatientIn vereinbart und getimed)
Arm B: NB=84 NFU1=76 NFU2=81 NFU3=74 CAU
|
Erhebungszeitpunkte Baseline Follow-Up1 (4 Wochen) Follow-Up1 (24 Wochen) Follow-Up2 (48 Wochen)
Primäre Endpunkte: 1. Rezidivangst (FCRI, melanom-spezifische Subskalen;)
Sekundäre Endpunkte: 1. Andere Subskalen des FCRI (Trigger, psychischer Distress, funktionelle Einschränkungen, Beruhigung (reassurance), Einsicht, Coping-Strategien 2. Depressivität 3. Angst 4. Stress 5. QoL (AQoL) 6. Melanom-relevantes gesundheitsverhalten 7. Zufriedenheit mit der Versorgung (CSQ)
|
1. Rezidivangst: à PE versus CAU: Follow-Up1: Sign. stärkere Reduktion in PE vs. CAU Follow-Up2: Sign. stärkere Reduktion in PE vs. CAU Follow-Up3: Sign. stärkere Reduktion in PE vs. CAU
2. Depressivität: à PE versus CAU: Keine sign. Gruppenunterschiede zu keinem der Zeitpunkte
3. Angst: à PE versus CAU: Keine sign. Gruppenunterschiede zu keinem der Zeitpunkte
4. QoL: à PE versus CAU: Keine sign. Gruppenunterschiede zu keinem der Zeitpunkte
|
Keine berichtet |
Cancer Institute New South Wales (NSW) Translational Program Grant, The National Depressivität Initiative, Sydney Catalyst Top-Up Research Scholar Award, National Health and Medical Research Council of Australia and Cancer Institute NSW, National Heart Foundation of Australia Future Leader Fellowship, Harkness Fellowship in Health Care Policy and Practice from the Commonwealth Fund, n NHMRC Sidney Sax Early Career Fellowship, NHMRC Senior Principal Research Fellowship
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: low
Geplante Fallzahl (N=154) erreicht |
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Jim et al., 2020: Internet-Assisted Cognitive Behavioral Intervention for Targeted Therapy–Related Fatigue in Chronic Myeloid Leukemia: Results From a Pilot Randomized Trial |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=44 Post-Treatment: N=41
ITT-Analyse ohne Imputation, Ausgewertet: N=41
Land: USA 2015-2017 |
Leukämie-Patienten, mit Fatigue (mind. >4 auf auf Fatigue Symptom Inventory)
Geschlecht: 48% weiblich
Alter: 29-82 Mittelwert: 55 |
Arm A: NB= 29 NP=27 KVT für therapiebezogene Fatigue (CBT-TTF)), ein face-to-face (90min) Gespräch zu Beginn, dann 45min über FaceTime/Ipad, je nach Wunsch/Bedarf wöchentlich oder alle 2 Wochen, über 18 Wochen
Arm B: NB= 15 NP=14 WL |
Erhebungszeitpunkte Baseline Post-Intervention
Primäre Endpunkte: 1. Fatigue (Fatigue Subscale des FACIT-F)
Sekundäre Endpunkte: 1. QoL (FACT-G) |
1. Fatigue: à CBT-TTF versus WL: Post-Treatment: Sign. Gruppenunterschiede zugunsten von CBT-TTF (d=1.07), Sign. höhere klinische Verbesserung in CBT-TTF (85% versus 29%)
2. QoL: à CBT-TTF versus WL: Post-Treatment: Für overall QoL sign. Gruppenunterschiede zugunsten von CBT-TTF (d=1.15), sign. höhere klinische Verbesserung in CBT-TTF (88% versus 54%)
|
Nicht berichtet |
National Cancer Institute, Population Research, Interventions, and Measurement Core Facility at the H. Lee Moffitt Cancer Center and Research Institute
AutorInnen sind BeraterInnen von und involviert in: RedHill BioPharma and Janssen Scientific Affair, Novartis, Takeda, Pfizer, Bristol-Myers Squibb, Jazz Pharma, Celgene, Agios, Astella, AbbVie; grants from Incyte outside the submitted work
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Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: low
Patienten in CBT-TTF sign. jünger à Alter als Kovariate berücksichtigt
Pilotstudie
Geplante Fallzahl (N=48 bei Post-Treatment) nicht erreicht |
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Bouchard et al., 2019: Brief report of a tablet-delivered psychosocial intervention for men with advanced prostate cancer: Acceptability and efficacy by race |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=192 Follow-Up1: N=170 Follow-Up2: N=154
ITT-Ansatz ohne Imputation; ausgewertet: N=170 (FU1), N=154 (FU2)
Land: USA 2013-2016 |
Advanced Prostatakrebs-Patienten mit Androgendeprivation (androgen deprivation therapy; ADT)
Geschlecht: 100% männlich
Alter: Mittelwert: 68,84 |
Arm A: NR=95 NFU1=84 NFU2=77 Kognitiv-behaviorales Stress Management (KVSM) via Tablet, in der Gruppe, einmal wöchentlich (90 min) für 10 Wochen, zwischen den Sitzungen Videos und didaktische Materialien
Arm B: NR=97 NFU1=86 NFU2=77 AC; Health Promotion (HP) Placebo, in der Gruppe, einmal wöchentlich (60min) für 10 Wochen, via Tablet
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Erhebungszeitpunkte Baseline Follow-Up1 (14 Wochen) Follow-Up2 (38 Wochen)
Primäre Endpunkte: 1. Medizinische Komorbiditäten (CCI) 2. Engagement und Akzeptanz der Behandlung 3. Prostatakrebsbezogene Angst (MAX-PC) |
1. Prostatakrebsbezogene Angst: à KVSM versus HP: Follow-Up1: Sign. Gruppenunterschiede zugunsten von KVSM
Follow-Up2: Keine sign. Gruppenunterschiede
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MAX-PC bei Baseline höher in der KVSM-Gruppe |
National Institutes of Health’s National Cancer Institute (grant number R01CA157809 to F.J.P., principal investigator). L.C.B. was funded by the National Institutes of Health’s National Cancer Institute training grant number T32CA193193
Laut Angabe keine COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: unclear AB: low RB: unclear
Geplante Fallzahl (N=150 bei FU2) erreicht |
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Dong et al., 2019: Telephone-based reminiscence therapy for colorectal cancer patients undergoing postoperative chemotherapy complicated with depression: a three-arm randomised controlled trial |
RCT, prospektiv, offen, monozentrisch, 3 Arme
Randomisiert: N=135 Post-Intervention: N= 135
Keine Drop-outs, daher ausgewertet: N = 135
Land: China, 2015-2016 |
Patienten mit Dickdarmkrebs mit postoperativer Chemotherapie, Depressivitätswert zwischen 50-70 (SDS)
Geschlecht: 50,4% weiblich
Alter: Mittelwert: 59,09 |
Arm A: NB=45 NP=45 Telefonische Reminiszenz-Therapie (TBR), 1x 20-40min pro Woche, 6 Wochen
Arm B: NB=45 NP=45 Telefonische PSU (TPSU), 1x 20-40min pro Woche, 6 Wochen
Arm C: NB=45 NP= CAU |
Erhebungszeitpunkte Baseline Post-Intervention
Primäre Endpunkte: 1. Depressivität (SDS und HAMD-24)
Sekundäre Endpunkte: 1. Angst (SAS und HAMA) 2. Subjektives Wohlergehen (MUNSH) 3. Wahrgenommene soziale Unterstützung (PSSS) |
1. Depressivität à TBR versus TPSU und CAU Post-Intervention: Sign. Gruppenunterschiede zugunsten von TBR; sign. Verbesserung in TBR aber nicht in TPSU und CAU
2. Angst à TBR versus TPSU versus CAU: Post-Intervention: Sign. Verbesserungen in TBR und TPSU, nicht in CAU; sign. Gruppenunterschiede von TBR und TPSU zu CAU zugunsten von TBR und TPSU; keine sign. Unterschiede zwischen TBR und TPSU
|
Keine berichtet |
Chinese Natural Science Foundation
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N=135) erreicht |
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Nelson et al., 2019: Cancer and Aging: Reflections for Elders (CARE): A pilot randomized controlled trial of a psychotherapy intervention for older adults with cancer |
RCT, prospektiv, offen, monozentrisch(?), 2 Arme
Randomisiert: N=59 Post-Intervention: N=55 Follow-Up: N=48
kA zu Analysemethode; ausgewertet: N=kA
Land: USA |
Krebspatienten (Lunge, Prostata, Brust, Lymphome, gynäkologisch), aktives Krebstreatment oder spätestens 6 Monate nach Beendigung des Treatments, mind. 70 Jahre alt, erhöhte Werte auf Distress-Thermometer/HADS/KPR (über 4/6/60)
Geschlecht: 53% weiblich
Alter: Mittelwert: 76 |
Arm A: NB=31 NP=28 NFU=25 Cancer and Aging: Reflexions for Elders (CARE), telefonbasierte Intervention um Stress zu reduzieren, 5 Sitzungen über 7 Wochen, je 45min
Arm B: NB=28 NP=27 NFU=23 Enhanced Social Work control (ESWC), auch ungefähr 5 Telefonate über 7 Wochen, 15-30min lang |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up (8 Wochen)
Primäre Endpunkte: 1. Depressivität (HADS) 2. Angst (HADS)
Sekundäre Endpunkte: 1. Demoralisierung (DS) 2. Coping (3 von 15 Subskalen des COPE) 3. Spirituelles Wohlergehen (FACIT Spiritual Well-being-Scale) Einsamkeit (UCLA LS-SF) |
1. Depressivität: à CARE versus ESWC: Post-Treatment: Sign. Gruppenunterschiede zugunsten von CARE (d=0,58)
Follow-Up: Keine sign. Gruppenunterschiede (d=0,28, p=0.2)
2. Angst: à CARE versus ESWC: Post-Treatment: Keine sign. Gruppenunterschiede (d=0,15)
Follow-Up: Keine sign. Gruppenunterschiede, aber Trend zu niedrigeren Werten in CARE (d=0,41, p=0.1)
3. Distress à CARE versus ESWC: Post-Treatment: Sign. Gruppenunterschiede zugunsten von CARE (d=0,48)
Follow-Up: Sign. Gruppenunterschiede zugunsten von CARE (d=0,42)
|
Arm A: CARE: SUEs: 0/31 UEs: 0/31
Arm B: ESWC: SUEs: 0/28 UEs: 0/28
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Silbermann Foundation; CALGB Foundation; Muriel Duenewald Lloyd Inspiration Fund; National Cancer Institute
COI: nicht berichtet |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Pilotstudie
Keine Fallzahlplanung
Am Anfang mit 7 Sitzungen gestartet, dann nach 7 Probanden in CARE und 4 Probanden in ESWC auf 5 Sitzungen reduziert
AutorInnen vermuten Selektionsbias
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Reese (2018): A randomized pilot trial of a couple-based intervention addressing sexual concerns for breast cancer survivors. |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N =29 (Dyaden) Post-Intervention : N=28 (Dyaden)
ITT-Ansatz ohne Imputation Ausgewertet: N = 28 (Dyaden)
Land: USA kA zum Zeitraum
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Brustkrebs-patientinnen und ihre Partner
Geschlecht: Patienten: 100% weiblich
Alter: Patienten: M = 54.1 Partner: M = 54.8
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Arm A: IE (Intimacy Enhancement) NR = 20 (Dyaden) NP=19 (Dyaden)
Edukation und Skills bzgl. Intimität und Partnerschaft per Telefon + Übungen für zuhause 4 x 60-75 Min., wöchentliche Sitzungen
Arm B: LHT (Living healthy together) NR = 9 (Dyaden) NP=9 (Dyaden) Unspezifische Edukation und Support per Telefon (Stress, Schlaf, Ernährung) 4x 60-75 Min., Wöchentliche Sitzungen |
Erhebungszeitpunkte Baseline Post-Intervention
Primäre Endpunkte: 1. Durchführbarkeit 2. Akzeptanz 3. Sexuelle Funktion (FSFI bzw. IIEF) 4. Sexuelle Zufriedenheit (PROMIS SexFS) 5. Sexueller Distress (FSDS-R) 6. Selbstwirksamkeit 7. Kommunikationsqualität bzgl Sex (DSCS) 8. Emotionale Intimität (PAIR) 9. Beziehungs-qualität (DAS-7) 10. Distress (IES-R) 11. Körperbild Distress (BIS) 12. Depressivität (PHQ-9) 13. Angst (GAD-7)
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Patientenoutcomes:
1. Sexuelle Funktion à IE vs. LHT Sign. verbesserte sexuelle Funktion zugunsten von IE (d=1.24)
2. Sexuelle Zufriedenheit à IE vs. LHT Sign. verbesserte sexuelle Zufriedenheit zugunsten von IE (d=1.75)
3. Distress à IE vs. LHT Kein sign. Unterschied
4. Depressivität à IE vs. LHT Kein sign. Unterschied
5. Angst à IE vs. LHT Sign. reduzierte Angst zugunsten von IE (d=-1.36)
|
Arm A: IE UEs: kA
Arm B: LHT SUEs: kA |
National Cancer Institute (USA)
Laut Angaben kein COI
|
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: low RB: low
Pilotstudie
Keine Fallzahlplanung
|
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Abrahams et al., 2017 : The Efficacy of Internet-Based Cognitive Behavioral Therapy for Severely Fatigued Survivors of Breast Cancer Compared With Care as Usual: A Randomized Controlled Trial |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=132 Post-Intervention: N=125
ITT-Ansatz mit multipler Imputation (LOCF); ausgewertet: N=132
Land : Niederlande 2014-2016 |
Brustkrebs, abgeschlossene Behandlung innerhalb der letzten 3 Monate, krankheitsfrei
Geschlecht : 100% weiblich
Alter : >=18 Mittelwert : 51,5 |
Arm A : NR=66 Nm=61 IKVT, 6 Monate, 3 face-to-face-sessions, 8 internetbasierte Module
Arm B : NR=66 Nm=64 CAU, Warteliste für face-to-face KVT |
Erhebungszeitpunkte Baseline Post-Intervention
Primärer Endpunkt : 1. Fatigue (CIS)
Sekundäre Endpunkte : 1. Funktionale Einschränkungen (SIP) 2. Distress (BSI)) 3. QoL (EORTC-QLQ-C30) |
1. Fatigue à IKVT versus CAU: Post-Intervention: Sign. Gruppenunterschiede zugunsten von IKVT (d=1.0, großer Effekt)
2. Distress à IKVT versus CAU : Post-Intervention: Sign. Gruppenunterschied zugunsten von IKVT (d=0.8, großer Effekt)
3. QoL à IKVT versus CAU: Post-Intervention: Sign. Gruppenunterschied zugunsten von IKVT (d=0.7, mittlerer Effekt) |
Arm A : IKVT SUEs : 5/66 UEs : 0/66
Arm B : CAU SUEs : 0/66 UEs : 2/66
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Dutch Pink Ribbon Foundation
Laut Angaben kein COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: low
Geplante Fallzahl (N=132) erreicht |
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Ashing et al., 2016: Exploring the efficacy of a paraprofessional delivered telephonic psychoeducational intervention on emotional well-being in African American breast cancer survivors |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=40 Post-Intervention: N=39
ITT-Ansatz mit Imputation; ausgewertet: N=40
Land: USA
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Afro-amerikanische Brustkrebsüberlende (AABCS; Stage 0-III innerhalb der letzten 6 Jahre)
Geschlecht: 100% weiblich
Alter: nicht berichtet
|
Arm A: NR=20 Nm=20 Telefonische PE (TPE), 4-6 Monate, 7 Domänen/telefonische Sessions (30-60min)
Arm B: NR=20 Nm=19 Nur Info-Buch (IB)
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Erhebungszeitpunkte Baseline Post-Intervention
Primäre Endpunkte: QoL (FACT-G G) |
1. QoL àTPE versus IB: Sign. Gruppenunterschied zugunsten von TPE
Sign. Verbesserung von TPE von Baseline zu Post-Intervention (+4 Punkte auf FACT-G Gesamtscore)
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Keine Angaben |
Department of Defense Breast Cancer Research program
Laut Angaben kein COI |
- Pilotstudie Keine Fallzahlplanung |
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DuHamel et al., 2016: The sexual health of female rectal and anal cancer survivors: results of a pilot randomized psycho-educational intervention trial |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N= 82 Follow-Up1: N=62 Follow-Up2: N=55
Ausgewertet: N=60 (FU1), N=54 (FU2) (keine Angabe, ob ITT)
Land: USA Registriert 2008 |
Abgeschlossene Behandlung, aktuell krankheitsfrei, Mastdarm- und Analkrebspatientinnen
Geschlecht: 100% weiblich
Alter: Mittelwert: 55,43 |
Arm A: NB=40 NFU1=27 NFU2=22
Cancer Survivorship Intervention-Sexual Health (CSI-SH), telefonbasiert, 4x 1h individuelle Sitzungen, für manche Mix aus face-to-face und Telefon, für manche nur Telefon
Arm B: NB=42 NFU1=35 NFU2=33 WL |
Erhebungszeitpunkte Baseline Follow-Up1 (16 Wochen) Follow-Up2 (32 Wochen)
Primäre Endpunkte: 1. Sexuelle Funktion ((FSFI)
Sekundäre Endpunkte: 1. Krebs-Distress (IES-R) 2. Distress (BSI) Gesunheitsbezogene QoL (EORTC-QLQ-C30) |
1. Sexuelle Funktion: à CSI-SH versus WL: Follow-Up1: Keine sign. Gruppenunterschiede (d=0.51)
Follow-Up2: Keine sign. Gruppenunterschiede (d=0.32)
2. Distress: à CSI-SH versus WL: Follow-Up1: Keine sign. Gruppenunterschiede
Follow-Up2: Keine sign. Gruppenunterschiede
3. QoL: à CSI-SH versus WL: Follow-Up1: Sign. Gruppenunterschiede zugunsten von CSI-SH für EF-Subskala
Follow-Up2: Sign. Gruppenunterschiede zugunsten von CSI-HS für EF-Subskala
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Höherer Dropout in der CSI-SH-Gruppe (8 vs. 1)
Mehr Probandinnen in der CSI-SH-Gruppe haben Trial nicht beendet (12 vs. 3) |
National Cancer Institute and the MSK Cancer Center Support Grant/Core Grant
Laut Angaben keine COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N=64) erreicht
Pilotstudie |
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Badr (2015): |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 39 Dyaden/ 78 Individuen Post-Intervention : N=38,5 Dyaden/77 Individuen
Keine Angabe ob ITT ; aber alle ausgewertet N = 39 Dyaden/78 Individuen
Land: USA kA zum Zeitraum |
Fort-geschrittener Lungenkrebs Patient & Partner/ andere primäre Betreuungs-person
Geschlecht: Patienten: 74% weiblich Partner: 69% weiblich
Alter: Patienten: 38-87 M: 68.17 Partner: 35-70 M: 51.1
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Arm A : NR=20 Dyaden/40 Individuen NP=20 Dyaden/40 Individuen
Telefonische Beratung 6x 60 Minuten 1x/Woche
Arm B : NR=19 Dyaden/38 Individuen NP=19 Dyaden/37 Individuen CAU |
Erhebungszeitpunkte Baseline Post-Intervention (2 Wochen Post-Intervention)
Primäre Endpunkte: 1. Psychisches Funktionsniveau 2. Belastung des Partners (Zarit Burden Interview)
Sekundäre Endpunkte: 1. Autonomie 2. Kompetenz 3. Verbundenheit |
1. Depressivität à EG vs. CAU Post-Intervention : Sign. Unterschied zugunsten der EG (d=-1.8)
2. Angst àEG vs. CAU Post-Intervention : Sign. Unterschied zugunsten der EG (d=-1.3) |
Arm A: EG UEs: kA
Arm B: KG SUEs: kA |
Forschungs-stipendium des Erstautors - Laut Angaben kein COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: low RB: unclear
Pilotstudie
Keine Fallzahlplanung |
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Casault et al., 2015: A randomized-controlled trial of an early minimal cognitive-behavioural therapy for insomnia comorbid with cancer |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=38 Post-Intervention: N=32 Follow-Up1: N=30 Follow-Up2: N=30
ITT-Ansatz ohne Imputation; Ausgewertet: N=35
Land: Frankreich Rekrutierung zwischen 2004 und 2005
|
Krebspatienten mit Insomnie und ohne Metastasen (80% Brustkrebs, 5% Dickdarmkrebs, 15% andere (Lungen-, Prostata-, Darm-, Zungen-, Vulva-Krebs))
Geschlecht: 92,1% weiblich
Alter: Mittelwert: 56,9 |
Arm A: NR=20 NP=16 NFU1=14 NFU2=14 Kurze selbstangewandte KVT für akute Insomnie (kKVT-I), 6 kurze Heftchen + 3 Telefonate mit Psychologe (30min), 6 Wochen
Arm B: NB=18 NP=16 NFU1=16 NFU2=16 CAU |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up1 (12 Wochen) Follow-Up2 (24 Wochen)
Primäre Endpunkte: 1. Schwere der Schlafprobleme (IIS) 2. Schwere der Insomnie (ISI) 3. Verschiedene Maße vom Schlaftagebuch
Sekundäre Endpunkte: 1. Depressivität (HADS-D) 2. Angst (HADS-A) 3. QoL (EORTC-QOL) 4. Schlafverhalten (SBQ) 5. Dysfunktionale Kognitionen und Einstellungen gegenüber Schlaf (DBAS) 6. Fatigue (MFI)
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1. Depressivität à kKVT-I versus CAU: Sign. Zeit x Gruppe Interaktion Prä-Post: Sign. moderate Reduktion in kKVT-I (d=–0.77) Prä-Follow-Up: Sign. moderate Verschlechterung in kKVT-I (d= 0.34)
2. Angst à kKVT-I versus CAU: Sign. Zeit x Gruppe Interaktion Prä-Post: Sign. moderate Reduktion in kKVT-I (d=–0.60) Prä-Follow-Up: Keine Sign. Veränderung in kKVT-I
3. Fatigue à kKVT-I versus CAU: keine sign. Zeit x Gruppe Interaktion Prä-Post: Sign. moderate Reduktion in beiden Gruppen (d=–0.5)
4. QoL à kKVT-I versus CAU: Keine sign. Zeit x Gruppe Interaktion Prä-Post: Sign. moderate Verbesserung in kKVT-I (d=0.67) Prä-Follow-Up: Keine Sign. Änderung in beiden Gruppen
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Nicht berichtet |
salary support awards from the Canadian Institutes of Health Research, held by the first and second authors, and by a research scientist award from the Fonds de la recherche en sante du Qu ebec held by the second author
|
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N=35) erreicht |
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Wenzel et al., 2015: Psychosocial Telephone Counseling for Survivors of Cervical Cancer: Results of a Randomized Biobehavioral Trial |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=204 Follow-Up1: N=168 Follow-Up2: N=151
kA ob ITT, aber fehlende Werte ausgeschlossen (listwise); Ausgewertet: N=139-145 (je nach Outcome)
Land: USA |
Gebärmutterhalskrebs-Patientinnen, Stage I-IV, seit min. 2 Monaten abgeschlossenes Treatment
Geschlecht: 100% weiblich
Geschlecht: Mittelwert: 43 |
Arm A: NB=115 NFU1=85 NFU2=76 Psychosoziales Telefon-Beratung (PTB), 5 wöchentliche Telefonate (20-60min) und einen monatlichen (?) Booster/einen Booster über einen Monat (?)
Arm B: NB=89 NFU1=83 NFU2=75 CAU
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Erhebungszeitpunkte Baseline Post-Intervention/Follow-Up1 (7 Wochen) Follow-Up2 (27 Wochen)
Primäre Endpunkte: 1. QoL (FACT-Cx)
Sekundäre Endpunkte: 1. Biomarker/Blutwerte 2. Depressivität (PROMIS & BSI) 3. Angst (PROMIS & BSI) 4. Distress (BSI-18) 5. Gynäkologische Probleme (GPC) 6. QoL Subskalen |
1. QoL: à PTB versus CAU: Keine sign. Gruppenunterschiede zu keinem MZP
2. Depressivität: à PTB versus CAU: Follow-Up1: Sign. Gruppenunterschiede zugunsten von PTB (auf PROMIS und BSI) (d=0.21–0.25)
Follow-Up2: Keine sign. Gruppenunterschiede (weder PROMIS noch BSI)
3. Angst: à PTB versus CAU: Keine sign. Gruppenunterschiede (weder PROMIS noch BSI) zu keinem MZP
4. Distress: à PTB versus CAU: Keine sign. Gruppenunterschiede zu keinem MZP
Es gab sign. Zeit x Gruppe x Behandlungsart-Interaktion für QoL und Depressivität (BSI) à Patientinnen mit OP schnellere Verbesserungen bis Follow-Up1, Patientinnen mit Chemotherapie langsamere Verbesserungen aber dafür größere Effektstärken bei Follow-Up2
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Nicht berichtet |
National Cancer Institute of the National Institutes of Health
Laut Angaben keine COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: high RB: unclear
Systematischer Drop-Out: Probandinnen mit hohem Depressionswert bei Baseline in der PTB-Gruppe wahrscheinlicher, Intervention aufzuhören (p<0.05)
Geplante Fallzahl (N=200) nicht erreicht |
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Keine Hinweise für höhere Wirksamkeit des Treatments (15/28) |
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Atema et al., 2019: Efficacy of Internet-Based Cognitive Behavioral Therapy for Treatment-Induced Menopausal Symptoms in Breast Cancer Survivors: Results of a Randomized Controlled Trial |
RCT, prospektiv, monozentrisch, offen, 3 Arme
Randomisiert: N=254 Follow-Up1: N=242 Follow-Up2: N=236
ITT-Ansatz mit Imputation (Mittelwertsersetzung); Ausgewertet: N=236-242 (je nach Outcome und MZP)
Land: Niederlande 2017-2019
|
Brustkrebs-Überlebende, abgeschlossene Behandlung, krankheitsfrei
Geschlecht: 100% weiblich
Alter: Mittelwert: 47,4 |
Arm A: NB=85 NP=82 NFU1=79 Angeleitete internetbasierte KVT (guided CBT - giCBT), 6 Wochen, zu Beginn ein telefonisches Gespräch + geschriebenes Feedback
Arm B: NB=85 NP=80 NFU1=77 Selbstangeleitete internetbasierte KVT (self-guided iCBT - siCBT), 6 Wochen, 1x wöchentlich 60min + täglich 30min Übungen
Arm C: NB=84 NP=80 NFU1=80 WL |
Erhebungszeitpunkte Baseline Post-Intervention/Follow-Up1 (4 Wochen) Follow-Up2 (18 Wochen)
Primäre Endpunkte: 1. Menopausale Symptome (FACT-ES) 2. Wahrgenommene Belastung durch Hot Flushes/Night Sweats (NF/HS; HFRS)
Sekundäre Endpunkte: 1. Schlafqualität (Groningen Sleep Quality Scale) 2. Häufigkeit von HF/NS (HFRS) 3. Sexuelle Funktion (SAQ) 4. Distress (HADS) 5. QoL (SF-36)
|
1. Sexuelle Funktion à Keine sign. Gruppenunterschiede in Veränderungsscore (t0-t1 und t0-t2)
2. Distress à keine sign. Gruppenunterschiede in Veränderungsscore (t0-t1 und t0-t2)
3. QoL à keine sign. Gruppenunterschiede in Veränderungsscore (t0-t1 und t0-t2) |
Keine Angaben |
Dutch Cancer Society (Grant No. NKI 2014-6788) and The Netherlands Cancer Institute
Laut Angaben kein COI
|
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: low
Geplante Fallzahl (N=192) erreicht |
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Chambers (2019): Five‐year outcomes from a randomised controlled trial of a couples‐based intervention for men with localised prostate cancer.
Chambers (2015): A randomised controlled trial of a couples-based sexuality intervention for men with localised prostate cancer and their female partners. |
RCT, prospektiv, multizentrisch, offen, 3 Arme
Randomisiert: N = 189 (Dyaden) Post-Intervention : N=161 (Dyaden) Follow-Up1 : N=159 (Dyaden) Follow-Up2 : N=144 (Dyaden) Follow-Up3 : N=106 (Patienten)/93 (Partnerinnen) Follow-Up4 : N=117 (Patienten)/101 (Partnerinnen) Follow-Up5 : N=111 (Patienten)/93 (Partnerinnen) Follow-Up6 : N=107 (Patienten)/91 (Partnerinnen)
ITT-Ansatz ohne Imputation; ausgewertet : siehe N bei MZP
Land: Australien 2009-2011 |
Prostatakrebs-patienten nach bzw. mit geplanter radikaler Prostata-ektomie + Partnerinnen
Geschlecht: Patienten: 100% männlich Partner: 100% weiblich
Alter: Patienten: M = 62.7 Partnerin: M = 59.8 |
Arm A: Nurse (Nurse counselling intervention) NR = 62 (Dyaden) NP=54 (Dyaden) NFU1=54 (Dyaden) NFU2=53 (Dyaden) NFU3=28 (Patienten)/35 (Partnerinnen) NFU4=kA (Patienten)/38 (Partnerinnen) NFU5=43 (Patienten)/37 (Partnerinnen) NFU6=41 (Patienten)/37 (Partnerinnen)
Telefonische Paar- und Sexualitäts-beratung durch geschultes Pflegepersonal 6-8 Sitzungen über 22 Wochen
Arm B: Peer (Peer support intervention) NR = 63 (Dyaden) NP=53 (Dyaden) NFU1=53 (Dyaden) NFU2=52 (Dyaden) NFU3=34 (Patienten)/31 (Partnerinnen) NFU4=40 (Patienten)/35 (Partnerinnen) NFU5=38 (Patienten)/34 (Partnerinnen) NFU6=41 (Patienten)/37 (Partnerinnen)
Telefonische Unterstützung durch geschulte Prostatakrebs Überlebende 6-8 Sitzungen über 22 Wochen
Arm C: CAU N R= 64 (Dyaden) NP=54 (Dyaden) NFU1=52 (Dyaden) NFU2=54 (Dyaden) NFU3=31 (Patienten)/27 (Partnerinnen) NFU4=33 (Patienten)/28 (Partnerinnen) NFU5=30 (Patienten)/22 (Partnerinnen) NFU6=28 (Patienten)/22 (Partnerinnen)
|
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up1 (12 Wochen) Follow-Up2 (36 Wochen) Follow-Up3 (84 Wochen) Follow-Up4 (132 Wochen) Follow-Up5 (180 Wochen) Follow-Up6 (228)
Primäre Endpunkte: 1. Inanspruchnahme erektiler Dysfunktions-behandlung 2. Sexuelle Funktion (IIEF) 3. Sexuelle Bedürfnisse (SCNS) 4. Sexuelles Selbst-bewusstsein (PIED) 5. Maskuliner Selbstwert (Masculine Self-Esteem scale) 6. Eheliche Zufriedenheit (DAS)
Sekundäre Endpunkte: Evaluation des Programms |
Patientenoutcomes:
1. Sexuelle Funktion à Nurse vs. CAU Keine sign. Unterschiede zu irgendeinem der Erhebungszeitpunkte |
Arm A: Nurse UEs: kA
Arm B: Peer SUEs: kA
Arm C: CAU SUEs: kA
|
Australian National Health and Medical Research Council
Laut Angaben kein COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: low RB: high
Keine Fallzahlplanung |
|
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Fox et al., 2019: Integrating PROMIS® Computerized Adaptive Tests Into a Web-Based Intervention for Prostate Cancer |
RCT; prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=192 Post-Intervention: N=115
ITT-Ansatz, kA zu Umgang mit fehlenden Werten; Ausgewertet: N=107-115 (je nach Outcome)
Land: USA 2013-2016 |
Advanced Prostatakrebs-Patienten (stage III-IV), mind. 1x Hormontherapie im vergangenen Jahr
Geschlecht: 100% männlich
Alter: Mittelwert: 71,31 |
Arm A: NB= 95 NP=50 Kognitiv-behaviorales Stress-Management-training (CBSM), Gruppe, 10 Wochen, 90min pro Sitzung, web-basiert (Videokonferenz über Tablets)
Arm B: NB= 97 NP=65 AC, Health Promotion (HP), web-basiert (Videokonferenz über Tablets), 10 Wochen, 60min pro Sitzung
|
Erhebungszeitpunkte Baseline Post-Intervention
Primäre Endpunkte: 1. Angst 2. Depressivität 3. Fatigue 4. Beeinrächtigungen durch Schmerzen 5. Physische Leistungsfähigkeit
Alle Outcomes gemessen über PROMIS; computerized adaptive testing (CAT) |
Keine sign. Gruppenunterschiede auf relevanten Endpunkten
Sign. Reduktion von Angst für HP |
Nicht berichtet |
NCI grant, NCI diversity supplement, NIH/NCI training grant, National Institutes of Health's National Center for Advancing Translational Sciences,
Laut Angaben keine COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: unclear AB: unclear RB: unclear
Feasibility-Studie
Keine Fallzahlplanung |
|
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Lim et al., 2019: Pilot trial of a STOMA psychosocial intervention programme for colorectal cancer patients with stomas |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=63 Mid-Intervention: N=51 Post-Intervention: N=51 Follow-Up: N=51
ITT-Ansatz ohne Imputation Ausgewertet: N=51
Land: Singapur 2015-2016 |
Darmkrebspatienten mit Katheter/Stoma
Geschlecht: 35,3%
Alter: 21-88 Mittelwert: 63 |
Arm A: NB=32 NM=27 NP=27 NFU=27 Psychosoziales Interventionsprogramm (STOMA), face-to-face psychoedukatives Treffen vor OP, Edukations-Broschüre, fünf Telefon-Follow-Ups (eines vor OP, die anderen 4 nach OP)
Arm B: NB=31 NM=24 NP=24 NFU=24 CAU |
Erhebungszeitpunkte: Baseline Mid-Intervention Post-Intervention Follow-Up 1 (1 Monat)
Primäre Endpunkte: 1. Stoma care Selbstwirksamkeit 2. Akzeptanz des Stomas 3. Stoma-Kompetenz 4. Länge des Krankenhausaufenthaltes 5. Angst (HADS-A) Depressivität (HADS-D) |
Keine sign. Gruppenunterschiede auf relevanten Endpunkten
|
Nicht berichtet |
Singapore Cancer Society (SCS) Cancer Research Grant 2013
Laut Angaben keine COI
|
Risk of Bias
SB1: low SB2: high PB: high DB: high AB: low RB: unclear
Geplante Fallzahl nicht erreicht (N=84)
Pilotstudie (da Fallzahl nicht erreicht)
" The study was designed to be a full RCT, with a plan to recruit 84 participants based on the power analysis (Lim et al., 2015). However, there was a large number of patients who rejected to participate in the study (N = 20) or did not meet the selection criteria (N = 33) during the funded time‐period in the participating hospital. Thus, the recruitment stopped at 53 participants. Therefore, this study was considered a pilot RCT." (p. 1340)
|
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Mosher (2019): Acceptance and Commitment Therapy for Symptom Interference in Advanced Lung Cancer and Caregiver Distress: A Pilot Randomized Trial. |
RCT prospektiv, multizentrisch, offen, 2 Arme
Randomisiert: N = 50 Follow-Up1: N = 38 Follow-Up2:
ITT-Ansatz ohne Imputation; ausgewertet: N=50
Land: USA
|
Lungenkrebs (Stadien III – IV) und deren Berzugs-personen
Geschlecht:
Alter: 35-82 Mittelwert: 63
|
Arm A: NB = 25 NFU1=20 NFU2=20 ACT, telefonbasiert, 6 Sitzungen, 50min, wöchentlich
Arm B: NB = 25 NFU1=18 NFU2=18 AC (Edukation, Unterstützung), telefonbasiert, 6 Sitzungen, 50min, wöchentlich |
Erhebungszeitpunkt Baseline Post-Intervention (2 Wochen) Follow-Up1 (6 Wochen)
Primäre Endpunkte: Funktionale Einschränkung durch Symptomlast: 1. Symptom Interferenz (MDASI) 2. Interferenz durch Fatigue (FSI) 1. Interferenz durch Schmerz (PROMIS) 2. Vermeidung aufgrund von Schwindel (PROMIS) 3. Angst (PROMIS) 4. Depressivität (PROMIS)
Sekundäre Endpunkte: Schwere der körperlichen Symptome: 5. Fatigue (PROMIS) 6. Schlafstörungen (PROMIS) 7. Schmerz (PROMIS) 8. Atembeschwerden (MSAS)
|
1. Angst àACT vs. KG Keine sign. Zeit-Gruppe-Interaktion
2. Depressivität àACT vs. KG
3. Fatigue (Schwere) àACT vs. KG Keine sign. Zeit-Gruppe-Interaktion
4. Schmerz (Schwere) àACT vs. KG Keine sign. Zeit-Gruppe-Interaktion 9. |
Arm A: ACT SUEs: kA UEs: kA
Arm B: KG SUEs: kA UEs: kA |
Walther Cancer Foundation + National Cancer Institute (USA)
Laut Angaben kein COI |
Risk of Bias
SB1: low SB2 unclear PB: high DB: unclear AB: low RB: unclear
Keine Fallzahlplanung
Pilotstudie
|
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Mosher et al., 2018: Acceptance and commitment therapy for symptom interference in metastatic breast cancer patients: a pilot randomized trial |
RCT, prospektiv, offen, monozentrische, 2 Arme
Randomisiert: N=47 Post-Intervention: N=39 Follow-Up: N=37
ITT Ansatz mit Imputation (LOCF) Ausgewertet: N=47
Land: USA 03-11/2016 (Rekrutierung) |
Metastasierte Brustkrebspatientinnen (Stage IV), mind. Eines der folgenden Symptome: Schmerz, Fatigue, Schlafstörung, Depressivität, Angst
Geschlecht: 100% weiblich
Alter: 25-75 Mittelwert: 56.3 |
Arm A: NB=23 NP=18 NFU=17 ACT, telefonisch, 6 Sitzungen
Arm B: NB=24 NP=21 NFU=24 Edukation/Unterstützung (ES), 6 Sitzungen |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (4 Wochen)
Primäre Endpunkte: 1. Globale Symptominterferenz (MDASI) 2. Schmerzinterferenzen (PROMIS) 3. Fatigue (FSI) 4. Schlafstörungen (PROMIS)
Sekundäre Endpunkte: 1. Schmerzintensität (PROMIS) 2. Fatigue (PROMIS) 3. Schlafstörungen (PROMIS) 4. Depressivität (PROMIS) 5. Angst (PROMIS)
|
Keine sign. Gruppenunterschiede auf relevanten Endpunkten
Aber: In ACT höhere Abnahme von Fatigue mit mittlerer Effektstärke in ACT (d=–0,43 versus d=–0,24 in ES) Für beide Gruppen Abnahme von Depressivität (ACT: d=–0.27 und ES: d=–0.28)
|
keine berichtet |
Walther Cancer Foundation, National Cancer Institute, Walther Cancer Foundation
Laut Angaben keine COI
|
Risk of Bias
SB1: low SB2: low PB: high DB: unclear AB: low RB: unclear
Pilotstudie
Keine Fallzahlplanung (kA)
In ACT-Gruppe höhere Baseline-Werte von globaler Symptom-Interferenz, Fatigue-Interferenz, Schlafstörung, schlafbezogene Beeinträchtigungen |
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Wise et al., 2018: Suffering in Advanced Cancer: A Randomized Control Trial of a Narrative Intervention |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=110 Post-Intervention: N=92 Follow-Up: N=86
PP-Analyse Ausgewertet: N=86
Land: USA |
Advanced cancer (Stage III oder IV), Treatment abgeschlossen (33% gynäkologisch, 16% Brust, 14% Darm, 12% Leber, 26% andere)
Geschlecht: Ca. 79% weiblich
Alter: 35-80 Mittelwert: 57 |
Arm A: NB=59 NP=49 NFU=49
miLivingStory,(miLS), telefonbasierte narrative Intervention in Form von Lebens- und Krankheits-Review; 3 Komponenten: 1) Telefoninterview (ein Kennenlernen, 20-30min und dann das Interview, 45-124min); 2) miLivingStory Website mit Infos etc.; 3) miLivingStory Social Network, um Geschichten auszutauschen
Arm B: NB=51 NP=43 NFU=37 miOwnResources (miOR); Kontrollwebsite, enthält miLivingStory Krebsinfos, aber keine Tipps in Form von eigenen/anderen Geschichten
|
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (8 Wochen)
Primäre Endpunkte: 1. Frieden und Bedeutsamkeit (peace and meaning; FACIT-Sp) 2. Depressivität (POMS-SF) 3. Wut (POMS-SF) 4. Angst (POMS-SF) |
1. Depressivität à miLS versus miOR: Post-Intervention: Keine sign. Gruppenunterschiede
Follow-Up: Keine sign. Gruppenunterschiede
2. Angst: à miLS versus miOR: Post-Intervention: Keine sign. Gruppenunterschiede
Follow-Up: Keine sign. Gruppenunterschiede |
Nicht berichtet |
National Cancer Institute
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: low
Geplante Fallzahl erreicht (N=80 zum Follow-Up-Zeitpunkt)
Möglicherweise nicht-repräsentative Stichprobe: geringe Teilnahme und hoher Drop-Out |
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Hass et al., 2017: Effekte der telefonischen Nachsorge in der onkologischen Rehabilitation nach Brustkrebs – Ergebnisse einer randomisierten Studie |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert (Baseline2): N=153 Post-Intervention: N=127
kA zu Analysemethode; Ausgewertet: N=127
Land: Deutschland
|
Brustkrebspatientinnen während der onkologischen Reha,
Geschlecht: 100% weiblich
Alter: 27-54 Mittelwert: 46,6 |
Arm A: NB2= 70 NP=53 Telefonische Nachsorge, nach Entlassung über 6 Monate. In 4-wöchigen Abständen, insgesamt 5 Gespräche à ca.15min
Arm B: NB2=83 NP=74 CAU, keine telefonische Nachsorge |
Erhebungszeitpunkt Baseline1 (Beginn stat. Reha) Baseline2 (Ende stat. Reha) Post-Intervention
Primäre Endpunkte: 1. Psychische Belastung (Emotional Thermometer) 2. QoL (LZI) 3. Indikatoren des Reha-Status (IRES-24) 4. Angst (HADS) 5. Depressivität (HADS) 6. Gesundheitsverhalten 7. Rückkehr an den Arbeitsplatz |
Keine sign. Gruppenunterschiede auf relevanten Endpunkten
|
Nicht berichtet |
Arbeitsgemeinschaft für Krebsbekämpfung NRW (ARGE)
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: high RB: unclear
Geplante Fallzahl (N=124) erreicht |
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Hummel et al., 2017: Efficacy of Internet-Based Cognitive Behavioral Therapy in Improving Sexual Functioning of Breast Cancer Survivors: Results of a Randomized Controlled Trial |
RCT, prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=169 Mid-Treatment: N=156 Post-Intervention: N=151
ITT-Ansatz mit Imputation (LOCF), ausgewertet: N=143-156 (je nach Outcome und MZP)
Land: Niederlande |
Brustkrebsüberlebende mit DSM-4-Diagnose von sexueller Dysfunktion, krankheitsfrei
Geschlecht: 100% weiblich
Alter: Mittelwert: 51,1 |
Arm A: NB= 84 NM=75 NP=69 IKVT, wöchentliche Sitzung, max. über 24 Wochen
Arm B: NB= 85 NM=81 NP=82 WL
|
Erhebungszeitpunkte: Baseline Mid-Treatment (10 Wochen) Post-Intervention
Primäre Endpunkte: 1. Sexuelle Funktion (FSFI total) 2. Sexueller Distress (FSDS-R) 3. Beziehungsintimität (PAIR)
Sekundäre Endpunkte: 1. Körperbild (QLQ-BR23) 2. Menopausale Symptome (FACT-ES ) 3. Eheliche Funktion (MMQ) 4. Distress (HADS total) 5. QoL (SF-36)
|
1. Sexuelle Funktion: à IKVT versus WL: Keine sign. Gruppe-Zeit-Interaktion
Kein sign. Gruppenunterschied zu keinem Zeitpunkt
2. Distress: à IKVT versus WL: Keine sign. Gruppe-Zeit-Interaktion
keine sign. Gruppenunterschiede zu keinem Zeitpunkt
3. QoL: à IKVT versus WL: Keine sign. Gruppe-Zeit-Interaktion
keine sign. Gruppenunterschiede zu keinem Zeitpunkt
|
Nicht berichtet |
Netherlands Cancer Institute
Laut Angabe keine COI |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: low
Geplante Fallzahl (N=130) erreicht |
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Lai et al., 2019: A Nurse-Led Care Program for Breast Cancer Patients in a Chemotherapy Day Center A Randomized Controlled Trial |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=124 Post-Intervention: N=120
ITT-Ansatz mit Imputation (Expectation Maximization Algorithmus); Ausgewertet: N=120
Land: China (Hong Kong) |
Brustkrebspatientinnen, die zum ersten Mal Chemotherapie bekommen
Geschlecht: 100% weiblich
Alter: Mittelwert: 51,13 |
Arm A: NB=60 NFU=58 Nurse-Led Care (NLC), ein face-to-face Treffen vor Chemo, dann 4 Telefongespräche nach Chemo (in der Woche des 1., 2., 4. und 6. Chemozyklus
Arm B: NB=64 NFU=62 CAU |
Erhebungszeitpunkt Baseline Follow-Up (4 Wochen)
Primäre Endpunkte: 1. QoL (FACT-G)
Sekundäre Endpunkte: 1. Selbstwirksamkeit (SUPPH)
|
1. QoL: àNLC versus CAU: Keine sign. Gruppenunterschiede
|
Nicht berichtet |
Central Research Grant from the Hong Kong Polytechnic University
Laut Angaben keine COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N=90) erreicht |
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Ferguson et al., 2016: A Randomized Trial of Videoconference-Delivered Cognitive Behavioral Therapy for Survivors of Breast Cancer With Self-Reported Cognitive Dysfunction |
RCT. Prospektiv, multizentrisch, offen, 2 Arme
Randomisiert: N=47 Post-intervention: N=36 Follow-Up: N=35
kA ob ITT; Ausgewertet: N=35
Land: USA |
Brustkrebs-überlebende mit long-term chemotherapy-realted dysfunctions (CRCD), momentan krankheitsfrei
Geschlecht: 100% weiblich
Alter: |
Arm A: NB=27 NP=22 NFU=22 KVT à Memory and Attention Adaptation Training (MAAT), 8 wöchentliche Sitzungen von je 30-45min, per Videokonferenz
Arm B: NB= 20 N=P14 NFU=13 Attention control (AC) à supportive Therapie, 8 wöchentliche Sitzungen von je 30-45min, per Videokonferenz |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up (8 Wochen)
Primäre Endpunkte: 1. Kognitive Einschränkung (PCI) 2. Kognitive Fähigkeiten (FACT-Cog)
Sekundäre Endpunkte: 1. Verarbeitungsgeschwindigkeit und verbales Gedächtnis (TBANS) 2. Angst (bezogen auf kognitive Beeinträchtigungen(MIA-A) 3. Fatigue (FACIT-F) 4. Funktionsfähigkeit (FACT-G) 5. Angst (DASS-21) 6. Depressivität (DASS-21) 7. QoL (FACTCog)
|
Keine sign. Gruppenunterschiede auf relevanten Endpunkten
|
Nicht berichtet |
e National Institutes of Health Office of Research on Women’s Health administrated by the National Cancer Institute
Ferguson hat Copyright mit US Copyright Office für die in dieser Studie verwendeten Treatment-Manuale
|
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: high RB: unclear
Geplante Fallzahl (N=48) nicht erreicht |
|
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Malmström et al., 2016: The effect of a nurse led telephone supportive care programme on patients’ quality of life, received information and health care contacts after oesophageal cancer surgery—A six month RCT-follow-up study
|
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=82 Baseline: N=80 Post-Intervention: N=74 Follow-Up 1: N=69 Follow-Up 2: N=59 Follow-Up 3: N=49
ITT-Ansatz mit Imputation (Mittelwertsersetzungen & Ersetzung nach Scoring Manual des Messinstruments) Ausgewertet: N=82
Land: Schweden 2009-2013 |
Speiseröhrenkrebs mit operativem Eingriff
Geschlecht: 21,95% weiblich
Alter: Mittelwert: 66,4 |
Arm A: NR=41 NB=41 NP=40 NFU1=38 NFU2=34 NFU3=26 Pflegerische telefonische Unterstützung nach Operation, über 6 Monate, 16x zwischen 5-15min
Arm B: NR=41 NB=39 NP=34 NFU1=31 NFU2=25 NFU3=23 CAU |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up 1 (6 Wochen) Follow-Up 2 (14 Wochen) Follow-Up 3 (22 Wochen)
Primäre Endpunkte: 1. QoL (EORTC-QLQ-C30 und QLQ-OG25) |
Keine sign. Gruppenunterschiede |
Nicht berichtet |
Södra sjukvårdsregionen [The Southern Regional Health Care Committee] and Vårdakademin [Academy of caring science] at Skåne University hospital
Laut Angaben keine COI |
Risk of Bias
SB1: unclear SB2: low PB: high DB: high AB: low RB: unclear
Keine Fallzahlplanung (kA) |
|
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Mosher et al., 2016: Randomized Pilot Trial of a Telephone Symptom Management Intervention for Symptomatic Lung Cancer Patients and Their Family Caregivers |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=106 Dyaden (N=106 Patienten, N=106 Behandelnde Post-Intervention: N=80 Patienten, N=80 Behandelnde Follow-Up: N=79 Patienten, N=72 Behandelnde
ITT-Ansatz; kA zu Imputationsmethode
Ausgewertet: N=106 Dyaden
Land: USA 03/2013-04/2015 (Rekrutierung) |
Symptomatische Lungenkrebspatienten und ihre Betreuungspersonen
Geschlecht: Patienten: 53% weiblich Betreuende: 73% weiblich
Alter: Patienten: 42-85 Behandelnde: 20-80 Mittelwert: Patienten: 62,72 Behandelnde: 56,54 |
Arm A: NB=51 Dyaden; NP=36 Patienten, NP=35 Behandelnde; NFU=35 Patienten, NFU=33 Behandelnde
Telefon Symptom Management Intervention (TSM), 4 wöchentliche Telefonate je 45min, bestehend aus KVT und emotionsfokussierte Therapie
Arm B: NB=55 Dyaden NP=44 Patienten, NP=45 Behandelnde; NFU=44 Patienten, NFU=45 Behandelnde
Edukation/Support (E-S), 4 wöchentliche Telefonate je 45min |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (4 Wochen)
Primäre Endpunkte: 1. Depressivität (PHQ-8) 2. Angst (GAD-7) 3. Schmerz (BPI Short Form) 4. Fatigue (FSI) 5. Atemlosigkeit und Distress bzgl. Atemlosigkeit (MSAS) |
Keine sign. Gruppenunterschiede auf relevanten Endpunkten
Keine sign. Gruppen- oder Zeit-Effekte oder Zeit-Gruppen-Interaktionen
à keine Verbesserung in beiden Gruppen |
Keine berichtet |
American Cancer Society, American Cancer Society Institutional Research grant, National Cancer Institute
Laut Angaben keine COI
|
Risk of Bias
SB1: low SB2: low PB: high DB: unclear AB: low RB: high
Geplante Fallzahl erreicht (N=42 Dyaden) |
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Freeman et al., 2015: A randomized trial comparing live and telemedicine deliveries of an imagery-based behavioral intervention for breast cancer survivors: reducing symptoms and barriers to care |
RCT prospektiv, multizentrisch, offen, 3 Arme
Randomisiert: N = 118
ITT-Ansatz Ausgewertet: N = 118
Land: USA 2008-2010 |
Brustkrebs-Überlebende, mindestens 6 Wochen nach abgeschlossener Behandlung
Geschlecht: 100% weiblich
Alter: Mittelwert: 55.44
|
Imaginationsbasierte Verhaltensintervention (Arm A & B): 1x/Woche à 4h, 1.-4. Sitzung: 25 Min. Theorie, 25 Min. Interaktion in Triaden 5. Sitzung: Präsentation ind. Beiträge & Feedback
Arm A: NB = 48 NP = 41 NFU = 40 Gruppenangebot Edukation + Imagination + Übungen (Life Delivery, LD), 50min (25min Input, 25min Interaktion), wöchentlich, 5 Wochen + Übungen zuhause
Arm B: NB = 23 NP = 19 NFU = 19 Wie oben, nur: Online-Gruppe, Telemedizin (telemedecine delivery, TD)
Arm C: NB = 47 NP = 44 NFU = 43
WL, Angebot der ERL-Intervention nach 3-Monats-Follow-Up
|
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (2 Monate)
Primärer Endpunkt: 1. Allg. QoL (SF-36): physisch (PCS), psychisch (MCS)
Sekundäre Endpunkte: 2. Krebsbezogene QoL (FACT-B) 3. Fatigue (FACIT-F) 4. Wahrgen. kogn. Funktionsfähigkeit (FACT-Cog) 5. Spirituelles Wohlbefinden (FACIT-Sp-Ex) 6. Distress (BSI-GSI) 7. Schlafstörungen (PSQI) |
1. Allg. QoL (psychisch) à LD vs. TD vs. WL: Keine sign. Effekte für Zeit, Gruppe, Zeit x Gruppe-Interaktion.
2. Krebsbezogene QoL à LD vs. TD vs. WL: Sign. Effekt für Zeit.
3. Fatigue à LD vs. TD vs. WL: Sign. Effekt für Gruppe. Keine sign. Effekte für Zeit, Zeit x Gruppe-Interaktion.
4. Distress à LD vs. TD vs. WL: Keine sign. Effekte für Zeit, Gruppe, Zeit x Gruppe-Interaktion.
|
Keine berichtet. |
Finanzierung durch Small Business Innovating Research-Subvention + Krebspräventions-Stipendium für Mitarbeitende (NCI grant)
Laut Angaben kein COI. |
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: low RB: unclear
Keine Fallzahlplanung |
|
|||||||||||||
|
Perz et al., 2015: A randomized trial of a minimal intervention for sexual concerns after cancer: a comparison of self-help and professionally delivered modalities |
RCT, prospektiv, offen, monozentrisch, 2 Arme
Randomisiert: N=88 Patienten, N=53 Partner Post-Intervention: N=69 Patienten, N=53 Partner Follow-Up: N=59 Patienten, N=31 Partner
kA zum Umgang mit Dropouts; Ausgewertet: N=kA
Land: Australien |
Krebspatienten oder Partner von Krebspatienten (81% sexuellen Krebstyp (Prostata, Brust, gynäkologisch)
Geschlecht: 53% weiblich
Alter: Mittelwert: 56.25 |
Arm A: NB= 45 Patienten, NB=25 Partner; NP=35 Patienten, NP=20 Partner; NFU=33 Patienten, NFU=20 Partner
Schriftliches Informationsmaterial zur Selbsthilfe (68 Seiten) + ein Telefonat/Skype-Beratungsgespräch (60min) (HP)
Arm B: NB= 43 Patienten, NB=28 Partner; NP=34 Patienten, NP=17 Partner; NFU=26 Patienten, NFU=13 Partner
Nur Informationsmaterial zur Selbsthilfe (SH)
|
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (6 Wochen)
Primäre Endpunkte: 1. QoL (SF-12) 2. Depressivität (HADS) 3. Angst (HADS) 4. Self-Silencing (STSS) 5. Zufriedenheit mit Beziehung (DAS) 6. Sexuelle Kommunikation (DSC) 7. Sexuelle Funktion (CSFQ-14) 8. Sexuelle Zufriedenheit („‘how satisfied are you with your sexual relationship?“)
|
Patient*innenoutcome Keine sign. Gruppenunterschiede auf QoL, Depressivität, Angst, Sexuelle Funktion, sexuelle Zufriedenheit |
Nicht berichtet |
Australian Research Council Linkage Grant, Cancer Council New South Wales and the National Breast Cancer Foundation, Westmead Hospital and Nepean Hospital
Keine COI laut Angaben
|
Risk of Bias
SB1: low SB2: unclear PB: high DB: high AB: high RB: low
kA zur Fallzahlplanung |
|
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Psychotherapeutische Paar- und Familieninterventionen
|
Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Merkmale untersuchter Studien |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Methodische Bemerkungen |
Evidenzklasse |
|
Hu et al. 2019: „Association between dyadic interventions and outcomes in cancer patients: a meta analysis“
Eingeschlossene Primärstudien:
Belgacem 2013 Schenker 2016 El Jawahri 2016 Jia 2012 Arden Close 2013 Clark 2013 Steel 2016 Arden Close 2013 Northouse 2005, 2007, 2013a, b Winters Stone 2015 Perz 2015 Lambert 2016 Badger 2011 Chen 2012 Couper 2015 Collinge 2013 Mosher 2016 Badger 2013 Badr 2015 McLean 2013 Heinrichs 2012
|
MA
Suchzeitraum: Bis Mai 2018
Datenbanken: PubMed EMBASE CINAHL Cochrane Central Chinese Biomedical Literature Database PsycINFO Web of Science Chinese National Knowledge Infrastructure Wanfang Data
Einschluss-kriterien: P: Erwachsene Krebspatienten + Angehörige oder Partner I: psychosozial-, kognitions- oder verhaltens-orientiert C: - O: u.a. QoL, Depressivität, Angst, Schmerz, Fatigue S: RCTs
23 RCTS N= 2404
|
RCTs
Erwachsene mit Krebs ab 18 Jahren, bei denen Angehörige oder Partner in der Therapie mit einbezogen wurden
Geschlecht: kA
Mittleres Alter: kA
|
Inhalte: 8x FOCUS (Mulitkomponenten Famiien-intervention) 7x Psycho-edukation 2x Körperliches Training 2x Palliativ-versorgung 1x Symptom Management
Format: 8x face to face 7x Telefonkontakt 8x Beides Frequenz: 3-52 Sessions
Dauer: 1h bis 12 Monate 1x "as long as needed"
Kontrollgruppen: 18 x TAU/UC 5x andere Familienintervention
|
Primäre Endpunkte: Patientenseitig 1. QoL 2. Fatigue 3. Schmerz 4. Angst 5. Depressivität 6. Hoffnungs-losigkeit 7. Verbundenheit 8. "Marital functioning" 9. Überlebensrate
Verwendete Skalen QoL SF-36 QUAL-E FACT-BMT TDL FACT-G QLIP-BR BHS SF-12 AQoL UCLA-PSI FACT QoL-BC PSS-FA SWB MHI
Fatique FACT-F MFI FSI
Depressivität BDI-II HADS SDS CES-D FACT-G PROMIS GAD-7 BPI
Angst PROMIS HADS SAS GAD-7 FACT-G
|
Patientenseitig 1. QoL 0 – 3 Monate Follow-Up 7 RCTs, N=742 I2 = 92%; SMD=0.53 [-0.02, 1.08, p=.06] Random-Effects Model
3 – 6 Monate Follow-Up 3 RCTs, N=364 I2 = 77%; SMD=0.19 [–0.34, 0.71, p=.49] Random-Effects Model
>6 Monate Follow-Up 4 RCTs, N=646 I2 = 56%; SMD=0.13 [–0.12, 0.37, p=.31] Random-Effects Model
2. Fatigue 0 – 3 Monate Follow-Up 7 RCTs, N=750 I2 = 42%; SMD=0.04 [-0.15, 0.24, p=.65] Random-Effects Model
3 – 6 Monate Follow-Up 6 RCTs, N=167 I2 = 0%; SMD=–0.20 [–0.51, 0.10, p=.19] Random-Effects Model
3. Schmerz 0 – 3 Monate Follow up 4 RCTs, N=374 I2 = 51%; SMD=-0.07 [-0.36, 0.22, p=.64] Random-Effects Model
3 – 6 Monate Follow up 1 RCT, N=27 I2 = na ; SMD=–0.66 [–1.44, 0.12, p=.10] Random-Effects Model
4. Angst 0 – 3 Monate Follow up 13 RCTs, N=1091 I2 = 81%; SMD=-0.42 [–0.70, –0.13, p<.01> Random-Effects Model
Studie mit hohem RoB exkludiert (Jia 2012): 12 RCTs, N=971 I2 = 46%; SMD=-0.30 [-0.48, -0.12, 95% CI] Random-Effects Model
5. Depressivität 0 – 3 Monate Follow up 17 RCTs, N=1216 I2 = 84%; SMD=-0.35 [–0.65, –0.05, p<.001> Random-Effects Model
Studie mit hohem RoB exkludiert (Jia 2012): 16 RCTs, N=1096 I2 = 46%; SMD=-0.26 [–0.39, –0.13, p<.001> Random-Effects Model
3 – 6 Monate Follow up 5 RCTs, N=227 I2 = 0%; SMD=-0.29 [–0.56, –0.03, p=.03] Random-Effects Model
|
Keine SUEs berichtet
RCTs berichten UEs nicht
|
Primärstudien: RCTs mit low RoB SB: 6 PB: 17 DB: 11 AB: 20 RB: 23 OB: 1
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,15, non-kritischer Dom. 1,3,8,10
Sensitivitäts-analysen: Ausschluss von Studien mit hohem RoB
Publikationsbias: Egger´s test for Publicationbias
|
1a |
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Vintila et al. 2019: „Effectiveness of couple psycho-oncological interventions in increasing patients and their partners´adaption to desease: A systematic review and a meta analysis“
Eingeschlossene Primärstudien:
Porter 2012, 2017 Robertson 2016 Heinrichs 2012 Manne 2016 Hsiao 2016 Northouse 2007 Mclean 2013 Anden-Close 2013 Kayser 2010 Baucom 2009 Kuijer 2004 Lampert 2016 Walker 2013 Couper 2015 Kalaitzi 2007 Manne 2005 McCorkle 2007 Porter 2009 Chambers 2015 Scott 2004
|
MA
Suchzeitraum: Januar 2000 bis September 2018
Datenbanken: PsycINFO Medline
Einschluss-kriterien: P: Erwachsene Krebspatienten + Partner I: Psychosoziale Paarintervention C: - O: Depressivität, Angst, Distress, QoL, Beziehungs-qualität S: RCTs
21 RCTS, N=2081 Patienten-Partner-Dyaden
|
RCTs
8x Brust 7x Prostata 3x Gemischte Krebsdiagnose 2x Gastrointestial 1x Eierstock
Geschlecht: kA
Mittleres Alter: 43 – 63
Länder: kA |
Inhalte: 18x Paartherapie 12x Edukation zu Krebs und Bewältigungs-mechanismen 8x Umgang mit emotionalen Problemen Davon 13x face-to-face 2x telefonabsiert 1x Videokonferenz 5x gemischt
Frequenz: 1 – 16 Sitzungen, M=6 Sitzungen Gesamtdauer: 45min – 16h, M=7h
Kontrollgruppen: TAU Psychoedukation Andere Intervention Neurtal writing Wait List
|
Primäre Endpunkte: Patientenseitig 1. Depressivität 2. Angst 3. Distress 4. QoL 5. Beziehungs-qualität
|
Patientenseitig 1. Depressivität Post Intervention: 8 RCTs, N=775 I2 = 77%; SMD=0.03 [–0.29, 0.35, 95% CI]
< 6 Monate Follow up: 7 RCTs, N=733 I2 = 0%; SMD=–0.08 [–0.22, 0.05, 95% CI]
> 6 Monate Follow-Up: 2 RCTs, N=775 I2 = 95%; SMD=0.87 [–0.84, 2.60, 95% CI]
2. Angst Post Intervention: 5 RCTs, N=580 I2 = 0%; SMD=–0.04 [–0.2, 0.11, 95% CI]
< 6 Monate Follow up: 4 RCTs, N=542 I2 = 77,5%; SMD=–0.43 [–0.85, –0.01, 95% CI]
> 6 Monate Follow-Up: 2 RCTs, N=295 I2 = 36%; SMD=–0.03 [–0.4, 0.34, 95% CI]
3. Distress Post Intervention: 7 RCTs, N=911 I2 = 62%; SMD=–0.21 [–0.46, 0.04, 95% CI]
< 6 Monate Follow up: 4 RCTs, N=822 I2 = 92%; SMD=0.59 [–0.3, 1.22, 95% CI]
> 6 Monate Follow-Up: 3 RCTs, N=659 I2 = 90%; SMD=–0.59 [–1.44, 0.24, 95% CI]
4. QoL Post Intervention: 9 RCTs, N=10 I2 = 81%; SMD=0.12 [–0.18, 0.44, 95% CI]
< 6 Monate Follow up: 5 RCTs, N=842 I2 = 6%; SMD=0.01 [–0.12, 0.15, 95% CI]
> 6 Monate Follow-Up: 6 RCTs, N=623 I2 = 86%; SMD=–0.29 [–0.79, 0.20, 95% CI
|
Keine SUEs berichtet
RCTs berichten UEs nicht
|
Primärstudien RCTs mit low RoB SB: 52% PB: keine Angabe DB: 10% AB: 90% RB: 100% OB: keine Angabe
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,11, non-kritischer Dom. 1,3,5,6,14,
Sensitivitäts-analysen: Nicht durchgeführt
Publikationsbias: Egger's Test durchgeführt, Ergebnisse nicht diskutiert
|
1a |
|
Wang et al. 2017: „The Efficacy of Couple-Based Interventions on Health-Related Quality of Life in Cancer Patients and Their Spouses: A Meta-analysis of 12 Randomized Controlled Trails“
Eingeschlossene Primärstudien:
Baucom, 2009 Keefe, 2005 Northouse, 2005 Northouse 2007 McLean, 2013 Campbell, 2007 Heinrichs, 2012 Kuijer, 2004 Manne, 2005 Badger, 2007 Northouse, 2013 McCorkle, 2007
|
MA
Suchzeitraum: Bis 10. Februar, 2015
Datenbanken: PubMed EBSCO PsycINFO CINAHL EMBASE China Biology Mediine China National Knowledge Infratructure
Einschluss-kriterien: P: Erwachsene Krebspatienten + Partner oder Angehörige I: Paar-basierte Intervention C: - O: HRQoL S: RCTs
12 RCTS, N=1417 Patienten
|
RCTs
Erwachsene Krebspatienten (Brust 4, Gemischt 5,Prostata 3)
Geschlecht: kA
Mittleres Alter: k.A
Länder : USA Kanada Deutschland Niederlande
|
Inhalte: 3x Psychoedukative Intervention 5x Skills-Training 4x Gemischte Intervention
Dauer: 2 Wochen bis 12 Monate
Kontrollgruppen: 11x UC 1x Warteliste |
Primäre Endpunkte
1. Körperliche Gesundheit 2. Depressivität 3. Angst 4. Hoffnungs-losigkeit 5. Beziehungs-zufriedenheit
Verwendete Skalen Depressivität BDI QSC-R23 CES-D MHI-D
Angst BSI SSoSQ FoPq MHI-A PANAS |
1. Depressivität àGesamteffekt: Post-Intervention: 6 RCTs, N=353, I2 = 89%; SMD=-2.15 [–4.25, 0.06, p=.044] Fail-Safe-N : 52 Random-Effects Model
àPsychoedukation I2 = 0%; SMD=-1.56 [-2.53, -0.18, p = .002] à Skills Training I2 = 53%; SMD=-3.7 [-8.23, -1.69, p = .19] à Gemischte Intervention I2 = - %; WMD=0.49 [-1.04, 2.02, p = .529]
2. Angst àGesamteffekt: Post-Intervention: 5 RCTs, N=345, I2 = 90%; WMD=-1.16 [-2.16, -0.16, p = .023] Fail-Safe-N : 255 Random-Effects Model
à Psychoedukation I2 = 50%; WMD=-1.3 [-1.41, -1.18, p <.001> à Skills Training I2 = 76%; WMD=-1.16 [–2.16, –0.16, p = .029]
à Gemischte Intervention WMD=-0.23 [–0.83, 0.37, p = .453]
|
Keine SUEs berichtet
|
Primärstudien PEDRO-Score poor: - fair: 5 good: 7 excellent: -
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7,9,11,13 non-kritischer Dom. 1,3,8,12
Sensitivitäts-analysen: Sign. Heterogenität in allen MAs; Sensitivitätsanalysen und Subgruppenanalysen durchgeführt
Publikationsbias: Eggerstest und das N-Fail-Safe Kriterium zeigen keinen signifikanten Publikations Bias
|
1a- |
|
Badr et al. 2013: "A systematic review and meta analysis of psychosocial interventions for couples coping with cancer"3
Eingeschlossene Primärstudien: Badger 2007 Baucom2004 Budin 2008 Campbell 2004 Canada 2006 Christensen 1983 Giesler 2005 Heinrichs 2011 Kalaitzi 2007 Kayser 2010 Keefe 2005 Kuijer 2004 Manne 2005 Manne 2011 McLean 2011 Mishel 2002 Neu 2003 Northouse 2007 Porter 2004 Porter 2011 Scott 2004 Ward 2009 |
SysRev & MA
Suchzeitraum: Januar 1980 bis Juli 2012
Datenbanken: PubMed
CENTRAL EMBASE PsycInfo Web of Sience LISTA (EBESCO) Einschluss-kriterien: P: Krebspatienten und ihre Partner I: Paar basierte Interventionen C: UC & AC O: QOL S: RCTs
23 RCTS, N=2415 Patienten
|
RCTs
7x Brustkrebs 7x Prostatakrebs 1x Gastrointestinal Krebs 1x Lungenkrebs 1x Bust- oder Gynäkologischer Krebs 5x Gemischt
Geschlecht: kA
Mittleres Alter: 40 – 64
|
Inhalte: Beratung Psychoedukation KVT MBT Paar-KVT Sexual Therapie EFT
2 – 10 Mal wöchentlich Follow up: 1 Monat – 12 Monate
Kontrollgruppen: 13 x UMC 6 x AC 2 x SC 1x „Gleiche Intervention aber nur für Patienten“ 1 x „Standart social work services“
|
Primäre Endpunkte: 1. QoL è Psychologische Outcomes è Physische Outcomes è Beziehung
|
1. QoL à Psychologisch Patient I2 = 31%; SMD=0.18 [0.05, 0.31, p = .01] Fail Safe N : 35 Partner I2 = 0%; SMD=0.18 [0.05, 0.31, p = .01] Fail Safe N : 10
à Physisch Patient I2 = 57%; SMD=0.31 [0.11, 0.50, p = .001] Fail Safe N : 68
à Beziehung Patient I2 = 0%; SMD=0.25 [0.11, 0.40, p = .001] Fail Safe N : 15 Partner I2 = 0%; SMD=0.22 [0.03, 0.11, p = .002] Fail Safe N : 3
2. QoL (Ausreißer "winsorized" einbezogen) à Psychologisch Patient I2 = 58%; SMD=0.25 [0.12, 0.32, p = .001] Fail Safe N : 76 Partner I2 = 0%; SMD=0.21 [0.08, 0.34, p = .001] Fail Safe N : 22
à Beziehung Patient I2 = 0%; SMD=0.28 [0.14, 0.43, p = .001] Fail Safe N : 32 Partner I2 = 0%; SMD=0.24 [0.06, 0.43, p = .01] Fail Safe N : 7
|
Keine SUEs berichtet
RCTs berichten UEs nicht
|
Primärstudien : In allen im Review eingeschlossenen Studien, wurden die Teilnehmer randomisiert auf die Gruppen zugeteilt
Vier Studien berichten von verblindeten versuchsleitern
14 Studien berichten von manualisierter Behandlung
15 Studien berichten von einer überwachten Behandlungsumsetzng
14 Studien berichtn von identischen Kontrollgruppen und Untersuchungsgrppen zum Startpunkt der Untersuchung
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7,9,13 non-kritischer Dom. 1,3,5,10,12
Sensitivitäts-analysen: Nicht durchgeführt
Publikationsbias: für Outcomes geprüft Funnel Plot und „trim and fill“
Bei den psychologischen Outcomes zeigen sich im Funnelplot Ausreißer
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1a- |
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Faller et al. 2013: "Effects of Psycho-Oncologic Interventions on Emotional Distress and Quality of Life in Adult Patients with Cancer: Systematic Review und Meta-Analysis."13
Eingeschlossene Primärstudien: 198 RCTs
|
MA
Suchzeitraum: May 2013
Datenbanken: CENTRAL Medline PsycInfo
Einschluss-kriterien: P: erwachsene Krebspatienten I: psychoonkologische Interventionen C: Aufmerkamkeits-Placebo, TAU/UC O: Distress, QoL, Depressivität, Angst S: RCTs
198 RCTS, N=22238 Patientinnen (218 Vergleiche in MA)
|
RCTs
Gemischte Krebsdiagnosen (80) Brustkrebs (78) Prostatakarz. (8) Gynekologisch (6) Melanom (5) Hematologischer Krebs (4) Andere (12) Nicht angegeben (5)
Geschlecht: Median 82% weiblich
Alter: Median 54 Jahre
Länder : USA (107) UK (18) Australien (12) Kanada (10) Schweden (9) Niederlande (7) Weitere (35)
|
Inhalte: Psychotherapie Einzel (55) Gruppe (42) Paar (10) Psychoedukation (19) Entspannungsverfahren (46) Einfache Informaationsgabe (23) Andere (12)
davon Einzel (119) Gruppe (66) Paar (8) Nicht angegeben (5)
Dauer/Frequenz/ Länge: 1-35 Sitzungen, Median 6 Sitzungen, Über 1-730 Tage, Median 42 Tage
Kontrollgruppen: TAU/UC Aufmerksamkeitskontrolle |
Primäre Endpunkte: 1. Distress 2. gesundheitsbezogene QoL 3. Depressivität 4. Angst |
1. Distress à Gesamteffekt Post-Intervention: 77 RCTs, N=? I2 = 73%; SMD=0.29 [0.20, 0.37, p <.001> Follow Up ≤6 Monate: 58 RCTs, N=? I2 = 56%; SMD=0.17 [0.09, 0.24, p <.001> Follow Up >6 Monate: 39 RCTs, N=? I2 = 32%; SMD=0.10 [0.04, 0.1, p =.003]
à Paartherapie Post-Intervention: 9 RCTs, N=? I2 = 0%; SMD=0.16 [0.02, 0.29, p =.021] Follow Up ≤6 Monate: 3 RCTs, N=? I2 = 65%; SMD=0.00 [–0.42, 0.41, p=.98] Follow Up >6 Monate: 5 RCTs, N=? I2 = 0%; SMD=0.01 [–0.16, 0.18, p =.91]
2. QoL à Gesamteffekt Post-Intervention: 66 RCTs, N=? I2 = 78%; SMD=0.26 [0.15, 0.37, p <.001> Follow Up ≤6 Monate: 47 RCTs, N=? I2 = 65%; SMD=0.22 [0.12, 0.33, p <.001> Follow Up >6 Monate: 27 RCTs, N=? I2 = 50%; SMD=0.18 [0.07, 0.28, p <.001>
à Paartherapie Post-Intervention: 5 RCTs, N=? I2 = 0%; SMD=0.11 [-0.06, 0.27, p =.2] Follow Up ≤6 Monate: 2 RCTs, N=? I2 = 0%; SMD=0.01 [–0.25, 0.27, p=.92] Follow Up >6 Monate: 3 RCTs, N=? I2 = 0%; SMD=0.02 [–0.2, 0.25, p =.88]
3. Depressivität à Gesamteffekt Post-Intervention: 72 RCTs, N=? I2 = 56.5%; SMD=0.33 [0.25, 0.41, p <.001> Follow Up ≤6 Monate: 40 RCTs, N=? I2 = 40.8%; SMD=0.2 [0.11, 0.28, p <.001> Follow Up >6 Monate: 26 RCTs, N=? I2 = 47.1%; SMD=0.14 [0.05, 0.24, p =.002]
à Paartherapie Post-Intervention: 4 RCTs, N=? I2 = 46%; SMD=0.27 [-0.06, 0.6, p =.11] Follow Up ≤6 Monate: 1 RCT, N=? I2 = ?; SMD=0.37 [ ?] Follow Up >6 Monate: 2 RCTs, N=? I2 = 0%; SMD=0.24 [–0.01, 0.49, p =.06]
4. Angst à Gesamteffekt Post-Intervention: 74 RCTs, N=? I2 = 60%; SMD=0.38 [0.29, 0.46, p <.001> Follow Up ≤6 Monate: 38 RCTs, N=? I2 = 73%; SMD=0.34 [0.2, 0.47, p <.001> Follow Up >6 Monate: 15 RCTs, N=? I2 = 33%; SMD=0.17 [0.06, 0.28, p =.003]
à Paartherapie Post-Intervention: 3 RCTs, N=? I2 = 16%; SMD=0.11 [-0.2, 0.42, p =.48] Follow Up >6 Monate: 1 RCT, N=? I2 = ?; SMD=0.26 [ ?] |
Nicht berichtet |
Primärstudien: RCTs mit low RoB SB: 51 PB: kA DB: kA AB: 122 RB: 141 OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2, 7, 13 non-kritischer Dom. 3, 10,
Sensitivitäts-analysen: Bei hoher Heterogenität (l²>70%) Ausschluss vjew. einer Studie aus MA & Moderatorenanalysen (u.A. Alter, Tumorart)
Weiterhin a priori geplante Subgruppenanalysen (siehe Hauptergebnisse)
Publikations-bias: Visuelle Prüfung der Funnel-Plots
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1a- |
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Brandao et al. 2014: „Psychological intervention with couples coping with breast cancer: A systematic review“
Eingeschlossene Primärstudien:
Baucom 2009 Christensen 1983 Heinrichs 2012 Kalaitzi 2007 Kayser 2010 Manne 2005/2007 Naaman 2008 Scott 2004 Wiesenthal 2006 Zimmermann 2011 |
SysRev
Suchzeitraum: 1975 bis Januar 2013
Datenbanken : CINAHL PsycInfo Acadamic Search Complete MEDLINE PsycArticles Behaviourial Science Collection
Einschluss-kriterien: P : Frauen, die an Brustkrebs leiden I : Paarintervention C: / O: gesundheits-bezogene, psychologische oder Beziehungsoutcomes S: RCTs
10 RCTS N = 679 Paare
|
RCTs
Mamma-Ca (Stage 0 – IIIa)
Geschlecht : 100% weiblich + Partner
Mittleres Alter: 40 - 54
Länder : USA Deutschland Griechenland Kanada Australien |
Inhalte:
5x CBT 2x Paar- und Sexualberatung/-therapie 1x Emotions-fokussierte Therapie 1x Kurzintervention 1x sonstiges
Davon 9x einzelne Paare 1x Paargruppen
Frequenz Wöchentlich bis zweiwöchentlich
Dauer 4 bis 20 Sitzungen 60 -120min pro Sitzung
Kontrollgruppen: 4x Tau/UC 2x Aktive Kontrolle 2x edukative Intervention |
Primäre Endpunkte: 1. Psychologisches Funktionsniveau 2. Physisches Funktionsniveau 3. Ehequalität 4. Sexuelle Funktion |
8/10 Studien fanden signifikante Unterschiede auf min. einem rel. Outcome zugunsten der Intervention
1. Sexuelle Funktion 4 Studien zeigten verbessertes sexuelles Funktionsniveau und Zufriedenheit |
Keine SUEs berichtet
RCTs berichten UEs nicht
|
Primärstdudien Nicht berichtet
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,4,7,9,13 non-kritischer Dom. 1,3,10,14,16
Sensitivitäts-analysen: Keine MA
Publikationsbias: Nicht diskutiert; Handsuche & graue Literatur in Suche einbezogen
|
1a- |
|
Griffin et al. 2013: „Effectiveness of Family and Caregiver Interventions on Patient Outcomes among Adults with Cancer or Memory-Related Disorders: A systematic Review“
Eingeschlossene Primärstudien:
Badger 2007 Badger 2011 Baucom 2009 Blanchard 1996 Budin 2008 Campbell 2004, 2007 Canada, 2005 Giesler 2005 Gutafson 2013 Kayser 2010 Keefe, 2005 Kozachik, 2001 Kurtz, 2005 Manne, 2005, 2007 Manne 2011 McCorkle 2007 McMillan 2007 Meyers 2011 Mishel 2002 Moskau 2008 Nezu 2003 Northouse 2005 Northouse 2007 Porter 2009 Porter 2011 Schover 2012 Stephenson 2007 Bass 2003 Belle 2006 Bourgeois 2002 Brodaty 2009 Burgener 1998 Burns 2003 Camberg 1999 Chang 1999 Gerdner 2002 Gitlin 2010a Gitlin 2010b Gitlin 2008 Gitlin 2003 Gitlin 2001 Ginyea 2006 Jirovec 2001 Logsdon 2010 Martin-Cool 2015 McCallion 1999 McCurry 2005 Mittelmann 2004 2006 Ostwald 1999 Quayhagen 2000 Robinson 2007 Teri 1997 Teri 2003 Teri 2005 Wray 2010 Wright 2001
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SysRev
Suchzeitraum 1980 bis Dezember 2012
Datenbanken : MEDLINE PsycINFO
Einschluss-kriterien: P: u.a. Erwachsene Krebspatienten I: Interventionen, die Familienmitglieder oder Pflegepersonen des erwachsenen Patienten eiinbeziehen C: Usual Care, Warteliste oder alternative aktive Behandlung O: u.a. QoL, Depressivität/Angst S: RCTs, nach 1995 publiziert
56 RCTs, davon 27 RCTs zu Krebspatienten, N=4195
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RCTs
Erwachsene mit Krebs und deren Angehörige
Geschlecht Patienten 39% weiblich Angehörige 61% weiblich
Mittleres Alter Patienten M=60, 46-71 Angehörige M=56, 49-62
Länder USA
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Von 27 RCTs verglichen 18 RCTs die Intervention mit TAU/UC
Inhalte 4x Telefon- oder internetbasierte Familienberatung 5x Paar-CBT 4x familien-unterstütze Patientenversorgung 4x familienzentrierte CBT 1x Spezial-intervention
Frequenz M=6 Sitzungen 3- 12 Sitzungen
Dauer M=6 Wochen 1 Woche – 5 Monate
Kontrollgruppe 18x TAU/UC
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Primäre Endpunkte: 1. QoL 2. Depressivität/Angst 3. Symptom-management |
1. QoL à Global QoL 0/6 Studien (N=1367) zeigen sign. Verbesserung zugunsten IG
2. Depressivität/ 2/9 Studien (N=1519) zeigen sign. Verbesserung zugunsten IG
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RCTs berichten UEs nicht
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Primärstudien Reporting Bias Gute Qualität : 0/18 Moderate Qualität: 15/18 Schlechte Qualität 3/18
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7 non-kritischer Dom. 1,16
Sensitivitäts-analysen: Nicht durchgeführt, Heterogenität der Studien tabellarisch dargestellt
Publikationsbias: "Publication bias is suspected if evidence is derived from a small number of commercially funded trials with small sample sizes and a small number of event." (p.114)
Keine Angaben zu Pub.-Bias für relevante Ergebnisse
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1a |
Psychotherapeutische Paar- und Familieninterventionen RCTs (2015 – 2020)
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Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Patienten-merkmale |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Finanzierung / Conflict of Interest |
Methodische Bemerkungen |
Evidenzklasse |
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Keine Hinweise für höhere Wirksamkeit des Treatments (5/5) |
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Manne (2019): Couple-focused interventions for men with localized prostate cancer and their spouses: A randomized clinical trial |
RCT prospektiv, monozentrisch, offen, 3 Arme
Randomisiert: N=237 (Dyaden) Post-Intervention: N=212 (Patienten)/208 (Partnerinnen) Follow-Up1: N=205 (Patienten)/203 (Partnerinnen) Follow-Up2: N=204 (Patienten)/198 (Partnerinnen)
ITT-Ansatz ohne Imputation; Ausgewertet:siehe N zu MZP
Land: USA kA zum Zeitraum |
Lokal begrenztes Prostatakarzinom
Patient & Partnerin
Geschlecht: Patienten: 100% männlich
Partnerinnen: 100% weiblich
Alter: Patienten: M = 61 (SD = 7.3) Partnerinnen: M = 57 (SD = 8.5) |
Arm A: IET NR = 80 (Dyaden) NP=78 (Patienten)/76 (Partnerinnen) NFU1=72 (Patienten)/71 (Partnerinnen) NFU2=73 (Patienten)/71 (Partnerinnen)
Intimitätsfördernde Therapie (IET); Jeweils 5 Paarsitzungen, 90 Minuten (mit Audio aufgenommen) und 1 Booster-Anruf 3 Wochen nach letzter Paarsitzung, 30-45 Minuten
Arm B: GHW NR = 76 (Dyaden) NP=64 (Patienten)/64 (Partnerinnen) NFU1=60 (Patienten)/60 (Partnerinnen) NFU2=61 (Patienten)/59 (Partnerinnen)
Allgemeine Intervention zu Stärkung von Gesundheit und Wohlbefinden (GHW); Jeweils 5 Paarsitzungen, 90 Minuten (mit Audio aufgenommen) und 1 Booster-Anruf 3 Wochen nach letzter Paarsitzung, 30-45 Minuten
Arm C: CAU NR = 81 (Dyaden) NP=70 (Patienten)/68 (Partnerinnen) NFU1=73 (Patienten)/72 (Partnerinnen) NFU2=70 (Patienten)/68 (Partnerinnen)
CAU
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Erhebungszeitpunkte Baseline Post-Intervention Follow-Up1 (7 Wochen) Follow-Up2 (19 Wochen)
Primäre Endpunkte: 1. Allgemeine psychische Verfassung (MHI-38) 2. Depressivität (PHQ-9) 3. Distress (IES) 4. Krebsbezogene Sorgen 5. Beziehungszufriedenheit (DAS) |
Patientenoutcomes
1. Depression à IET vs. GHW vs. CAU Post-Intervention, FU1 und FU2: Keine sign. Zeit X Gruppe-Interaktion, sign. Zeiteffekt (Verbesserung in allen Gruppen bis einschl. FU1)
2. Krebsbezogene psychische Belastung à IET vs. GHW vs. CAU Post-Intervention, FU1 und FU2: Keine sign. Zeit X Gruppe-Interaktion, sign.r Zeiteffekt (Verbesserung in allen Gruppen bis einschl. FU1)
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Arm A: EG UEs: kA
Arm B: EG SUEs: kA
Arm C: CAU SUEs: kA |
Laut Angaben kein COI |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: unclear RB: low
Geplante Fallzahl (N=469 (Dyaden)) nicht erreicht.
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Ammari et al., (2018) : Results from the family and coping oriented palliative homecare intervention study (FamCope) – a randomized controlled trial
|
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=57 Post-Intervention N=38 Follow-Up N=30
ITT-Ansatz ohne Imputation
Land: Dänemark: Oct 2011-April 2013 |
Prostatakrebs (33%), Lungenkrebs (25%), Unterer Magen-Darm-Krebs (19%) (Stadium III –IV)
Geschlecht: 32% weiblich
Alter: Mittelwert: 67.4 |
Arm A: NR=28 NP=21 NFU=14 Familien intervention (FamCope) 6 Sitzungen, dreiwöchentlich
Arm B: NR=29 NP=17 NFU=16 CAU
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Erhebungszeitpunkt Baseline Post-Intervention Follow-Up (8 Wochen)
Primäre Endpunkte: 1. QoL (EORTC QLQ-C30 – Global Health Status)
Sekundäre Endpunkte 2. Angst (HADS) 3. Depressivität (HADS) |
Patientenoutcomes: 1. QoL à FamCope vs CAU: Post Intervention: keine sign. Gruppenunterschiede
Follow-Up: keine sign. Gruppenunterschiede
2. Angst à FamCope vs CAU: Post Intervention: keine sign. Gruppenunterschiede
Follow-Up: keine sign. Gruppenunterschiede
3. Depressivität à FamCope vs CAU: Post Intervention: keine sign. Gruppenunterschiede
Follow-Up: keine sign. Gruppenunterschiede
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Keine Angaben zu UEs |
Danish Cancer Society, Lundbeck Foundation, The Health Foundation (Helsefonden, Novo Nordic Foundation, Danish Nurses Organozatio, Danish Regions
Laut Angaben kein COI |
Risk of Bias
SB1: low SB2 low PB: high DB: high AB: low RB: low
geplante Fallzahl nicht erreicht (N=252)
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McCaughan (2018): Evaluating a psychosocial intervention for men with prostate cancer and their partners: Outcomes and lessons learned from a randomized controlled trial |
RCT, prospektiv, monozentrisch, 2 Arme
Randomisiert: N=17 (Dyaden) Post-Intervention: N=15 (Dyaden)/31 (ProbandInnen) Follow-Up: N=14 (Dyaden)/29 (ProbandInnen)
kA zu Analysemethode, aber wahrscheinlich ITT ohne Imputation; ausgewertet: Post-Intervention: N=16 (Patienten)/15 (Partner) Follow-Up: N=14 (Patienten)/14 (Partner)
Land: Nordirland kA zum Zeitraum
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Prostatakarzinom
Patient & Partnerin
Geschlecht: Patienten: 100% männlich
Partnerinnen: 100% weiblich
Alter: Patienten: EG: 56-79, KG: 56-71, M = 63.8
Partnerinnen: EG: 54-76, KG: 50-74, M = 60 |
Arm A: CONNECT NR = 13 (Dyaden) NP=12 (Dyaden) NFU=12 (Dyaden)
CONNECT-Intervention für Paar: 5 Einheiten über 9 Wochen: 3 Gruppensitzungen à 2 Stunden (Woche 1, 3, 9), 2 Telefonsitzungen (Woche 5, 7)
Arm B: TAU NR = 4 (Dyaden) NP=3 (Dyaden)/7 ProbandInnen NFU=2 (Dyaden)/5 ProbandInnen
TAU |
Erhebungszeitpunkte Baseline Post-Intervention Follow-Up (4 Wochen)
Primäre Endpunkte: 1. Selbstwirksamkeit (CASE, modifiziert) 2. Lebensqualität (FACT-G) 3. Symptom Distress (OSQ, Symptom Skala) 4. Kommunikation über Erkrankung (Lewis Mutually and Interpersonal Scale) 5. Unsicherheit bezüglich der Krankheitserfahrung (MUIS, modifiziert) 6. Nutzen der Erkrankung (Helgeson Benefits of Illness Scale) Soziale Unterstützung (Social Support Scale) |
1. Lebensqualität à CONNECT vs. TAU Post-Intervention und Follow-Up: Keine sign. Zeit x Gruppe-Interaktion
2. Symptom Distress à CONNECT vs. TAU Post-Intervention und Follow-Up: Keine sign. Zeit x Gruppe-Interaktion
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Arm A: EG UEs: kA
Arm B: KG SUEs: kA
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Finanzierung durch Cancer Focus Northern Ireland |
Risk of Bias
SB1: unclear SB2: unclear PB: high DB: high AB: high RB: high
Keine Fallzahl-planung
Ungleiche Randomisierung zu EG und KG aufgrund schleppender Teilnahme |
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Nicolaisen (2018): The effect of an attachment-oriented couple intervention for breast cancer patients and partners in the early treatment phase: A randomised controlled trial |
RCT prospektiv, multizentrisch, 2 Arme
Randomisiert: N=199 (Dyaden) Post-Intervention: N=163 (Dyaden)/ Follow-Up: N=141 (Dyaden)/
ITT-Ansatz ohne Imputation; Ausgewertet: Post-Intervention N=165 (Patienten)/ Follow-Up: N=145 (Patienten)/
Land: Dänemark 2012-2013
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Kürzlich diagnostizierte Patientinnen mit primärem Brustkrebs
Patientinnen & Partner
Geschlecht: Patienten: 100% weiblich Partner: 100% männlich
Alter: EG: Patienten: 27-79, M = 54.2 Partner: 28-92, M = 57.4
KG: Patienten: 31-75, M = 52.6 Partner: |
Arm A: HiH NR = 102 (Dyaden) NP=87 (Dyaden)/88 (Patienten)/87 (Parnter) NFU=80 (Dyaden)/82 (Patienten)/81 (Partner)
Hand in Hand (HiH) Intervention zusätzlich zu TAU: 4-8 Paarsitzungen bis zu 5 Monate nach OP
Arm B: TAU NR = 96 (Dyaden) NP=76 (Dyaden)/78 (Patienten)/78 (Partner) NFU=61 (Dyaden)/65 (Patienten)/63 (Partner)
TAU |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (20 Wochen)
Primärer Endpunkt: 1. Distress (IES)
Sekundäre Endpunkte: 2. Depressivität (HADS-D) 3. Angst (HADS-A) 4. Anpassung des Paars (dyadic adjustment) (RDAS) 5. Therapeutische Beziehung (“Bond”-Skala, WAI-SR)
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Patientenoutcomes
1. Distress à HiH vs. TAU Post-Intervention: Kein sign. Gruppenunterschied FU: Kein sign. Gruppenunterschied
2. Depressivität à HiH vs. TAU Post-Intervention: Kein sign. Gruppenunterschied FU: Kein sign. Gruppenunterschied
3. Angst à HiH vs. TAU Post-Intervention: Kein sign. Gruppenunterschied FU: Kein sign. Gruppenunterschied
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Arm A: EG UEs: kA
Arm B: KG SUEs: kA
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Laut Angaben kein COI.
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Risk of Bias
SB1: high SB2: low PB: high DB: high AB: unclear RB: high
Geplante Fallzahl (N=166) (knapp) nicht erreicht
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Couper (2015): Cognitive existential couple therapy (CECT) in men and partners facing localised prostate cancer: a randomised controlled trial |
RCT prospektiv, multizentrisch, offen, 2 Arme
Randomisiert: N = 62 (Dyaden) Post-Intervention: N=61 (Dyaden) Follow-Up: N=49 (Dyaden)
ITT-Ansatz mit Imputation (LOCF); ausgewertet: N=61 (Dyaden)
Land: Australien 2010-2012 |
Lokal begrenztes Prostatakarzinom, Stadium I-III
Geschlecht: Patienten: 100% männlich
Partnerinnen: 100% weiblich
Alter: Patienten: Mittelwert: 64,52
Partnerinnen: Mittelwert: 61,03
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Arm A: CECT NR=30 NP=29 NFU=23 Kognitiv-existentielle Paartherapie (Cognitive existential couple therapy (CECT)); 6 Wochen, 1x wöchentlich, 60-90 Minuten
Arm B: TAU NR=32 NP=32 NFU=26 TAU |
Erhebungszeitpunkte Baseline Post-Intervention (4 Wochen nach Intervention) Follow-Up (30 Wochen)
Primärer Endpunkt: 1. Funktionsweise der Beziehung (FRI)
Sekundäre Endpunkte: 2. Coping (Brief COPE) 3. Distress (IES-R) 4. Allgemeine mentale Gesundheit (MHI) |
1. Distress à CECT vs. TAU Post-Intervention und FU: Keine sign, Gruppenunterschiede
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Arm A: EG UEs: kA
Arm B: TAU SUEs: kA |
Laut Angaben kein COI |
Risk of Bias
SB1: low SB2: low PB: high DB: high AB: low RB: unclear
Geplante Fallzahl erreicht (für Post-Intervention) |
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Spezifische psychoonkologische Interventionen in der Palliativphase - Systematische Übersichtsarbeiten (2010 – 2020)
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|
Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Merkmale untersuchter Studien |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Methodische Bemerkungen |
Evidenzklasse |
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Li et al. 2020: "Effectiveness of dignity therapy for patients with advanced cancer: A systematic review and meta-analysis of 10 randomized controlled trials."1
Eingeschlossene Primärstudien: Vuksanovic 2017 Chochinov 2011 Hall 2012 Xingming 2016 Zhiyang 2015 Rongming 2016 Xiaodong 2018 En-gui 2018 Yanli 2018 Li 2018 |
MA
Suchzeitraum: Bis März 2019
Datenbanken: CBM CENTRAL PubMed Embase Web of Science ICTRP ClinicalTrials.gov opengrey.org
Einschluss-kriterien: P: "Advanced cancer patients" I: Dignity Therapy C: Standard Care O: Distress, Angst, Depressivität, QoL S: RCTs
10 RCTS, N=904 Patienten
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RCTs
Erwachsene Krebspatienten versch Tumorstadien (Gemischt 6, Brust 1, Lunge 2, Hepatozelluläres karzinom 1)
Geschlecht: 52% weiblich
Mittleres Alter: 49 - 84
Länder : China (70%) Australien Kanada UK |
Inhalte: Dignity therapy
Länge & Frequenz: 10 Tage – 2 Monate
kA zu Häufigkeit, Sitzungsdauer
Kontrollgruppen: 6x Routine Care 2x Standard Care 1x Standard Palliative Care 1x Standard psychological care |
Primäre Endpunkte: 1. Angst 2. Depressivität
Sekundäre Endpunkte: 3. Distress 4. QoL
Verwendete Messinstrumente: Angst HAMA HADS PDI SAS SCL-90
Depressivität HADS HAMD PDI SDS SCL-90
Distress PDI
QoL FACIT
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1. Angst àGesamteffekt: Post-Intervention: 9 RCTs, N=868, I2 = 91 %; SMD=−1.07 [−1.57, −0.58, p < .05] GRADE: very low
2. Depressivität àGesamteffekt: Post-Intervention: 10 RCTs, N=904, I2 = 94 %; SMD=−1.31 [−1.92, –0.70, p < .05] GRADE: very low
3. Distress àGesamteffekt: Post-Intervention: 4 RCTs, N=307, I2 = 68%; MD=−7.30 GRADE: very low
4. QoL àGesamteffekt: Post-Intervention: 2 RCTs, N=255, I2 = 0 %; SMD=−0.05 GRADE: moderate |
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 3 PB: 0 DB: 2 AB: 10 RB: 9 OB: 7
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2, 7 non-kritischer Dom. 3
Sensitivitäts-analysen: Effekte robust gegenüber Entfernung jeweils einer Studie
Starke Heterogenität der Ergebnisse
Publikations-bias: Visuelle Prüfung Funnel-Plot + Egger's Test liefern keine Hinweise auf Publ. bias |
1a |
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Warth et al. 2019: "Brief psychosocial interventions improve quality of life of patients receiving palliative care: A systematic review and meta-analysis."2
Eingeschlossene Primärstudien: Ando 2010 Chochinov 2011 Duggleby 2007 Hall 2011 Hilliard 2003 Horne-Thompson 2008 Lloyd-Williams 2018 Mok 2012 Ng 2016 Domingo 2015 Steinhauser 2017 Vuksanovic 2017 Warth 2015 Xiao |
MA
Suchzeitraum: Bis Dezember 2017
Datenbanken: CBM CENTRAL PubMed Embase Web of Science ICTRP ClinicalTrials.gov opengrey.org
Einschluss-kriterien: P: Fortgeschrittene terminale Erkrankung, min. 50% Krebs, ambulant- oder stationär-palliative Behandlung I: max. 4 Sitzungen und max 21 Tage, psychosoziale Intervention, vermittelt durch prof. Therapeut C: Wartelste, Tau/UC, Attention placebo O: QoL, Distress S: RCTs & CCTs
15 RCTS, N=1248 Patienten
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RCTs (und 1 CCT)
Fast ausschließlich erwachsene Krebspatienten, fortgeschrittenes Tumorstadium, palliativ behandelt
Geschlecht: zwischen 34% und 71% weiblich
Mittleres Alter: 47 -75
Länder : USA Asien Europa Australien |
Inhalte: 4x Dignity therapy 4x Musiktherapie 3x Sinnbasierte Interventionen 3x Lebensrück-schau ("life review")
Länge & Frequenz: Median von 2 Sitzungen; Sitzungsdauer 20 bis 90min
Kontrollgruppen: 8x TAU/UC 4x Aktive Kontrollgruppe 3x dreiarmiges Design mit Tau/UC und Aktiver Kontrolle |
Primäre Endpunkte: 1. QoL
Sekundäre Endpunkte: 2. Emotionaler Distress 3. Existentieller Distress
Verwendete Messinstrumente: QoL Single-Item Scales HQLI-R DT
Emotionaler Distress HADS FACT-G QoLC-E HQLI-R
Existentieller Distress FACIT-SP HHI QoLC-E
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1. QoL àGesamteffekt: Post-Intervention: 8 RCTs, I2 = 60 %; SMD=0.36 [0.08, 0.64, p = .02] à Ausschluss von Domingo 2015 und Xiao 2013 nach sig. Egger's-Test aufgr. großer Effekte à verbl. Heterogenität erklärt durch Moderator "inpatient setting" (SMD=0.61, n=5) vs. "outpatient setting" (SMD=0.04, n=3)
2. Emotionaler Distress àGesamteffekt: Post-Intervention: 15 Effekte, I2 = 73 %; SMD=−0.51 [−0.77, –0.26, p < .01] à keine Moderatoren erklären Heterogenität
3. Existentieller Distress àGesamteffekt: Post-Intervention: 11 Effekte, I2 = ?%; SMD=−0.40 à Ausschluss von Ando 2010 nach sig. Egger's-Test aufgr. großen Effekts à verbl. Heterogenität erklärt durch Moderator "measurement instrument" (FACIT-SP signifikant geringere Effekte als andere FraBö)
|
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 8 PB: 0 DB: 3 AB: 3 RB: 3 OB: kA
Review: AMSTAR-2: low quality Method.Mängel in kritischer Domäne 7 non-kritischer Dom. 3
Sensitivitäts-analysen: durchgeführt
Starke Heterogenität der Ergebnisse / Entfernung einflussreicher Studien / Moderatoren-analyse
Publikations-bias: Visuelle Prüfung Funnel-Plot + Egger's Test |
1a |
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Bauereiß et al. 2018: "Effects of existential interventions on spiritual, psychological, and physical well-being in adult patients with cancer: Systematic review and meta-analysis of randomized controlled trials."3
Eingeschlossene Primärstudien: Ando 2010 Breitbart 2010, 2012, 2015 Carlson 2016, 2013 Chochinov 2011 Classen 2001 Butler 2009 Giese-Davis 2002 Classen 2008 Dubbleby 2007 Gagnon 2015 Goodwin 2001 Bordeleau 2003 Hall 2011 Henry 2010 Herth 2000 Ho 2016 Juliao 2013, 2014 Kissane 2003, 2007 Lee 2006 Lloyd-Williams 2013, 2018 Lo 2016 Mok 2012 Rutsoen 1998 Spiegel 1981 Tabrizi 2016 Van der Spek 2017 Vuksanovic 2017 Xiao 2013 Ye 2017
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MA
Suchzeitraum: Januar 2018
Datenbanken: Medline PsychInfo Psyndex Embase CINAHL CENTRAL ICTRP
Einschluss-kriterien: P: erwachsene Krebspatienten I: "existential interventions" C: aktive & inaktive Kontrolle O: Primär: Spirituelles Wohlbefinden, Angst, Depressivität S: RCTs
30 RCTS, N=3461 Patientinnen (24 RCTs in MA)
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RCTs
Fortgeschrittene krebserkrankung (22) Frühstadium (4) Rezidivierende Krebserkrankung (1) Krebs-Überlebende (3) Gemischte Stichprobe mit anderen terminalen Erkrankungen (Krebs >90%) (2)
Geschlecht: kA
Mittleres Alter: 57
Länder : USA (7) Japan (1) Kanada (9) Australien (4) UK (3) China (4) Portugal (1) Norwegen (1) Iran (1) Niederlande (1)
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Inhalte: Sinnbasierte Interventionen (9) Supportiv-expressive Gruppenth. (9) Kognitiv-existentielle Therapie (2) "Life Review" (4) "dignity therapy" (4)
davon Einzel (14) Gruppe (15) Beides (1)
Dauer/Frequenz/ Länge: 1 – 52 Wochen bei wöchentlicher Frequenz
Kontrollgruppen: Warteliste oder TAU/UC (18) Massage, Entspannung, Stress management (3) Supportive therapie (5) Psychoedeukation (3) "Mindfulness-based cancer recovery" (1) |
Primäre Endpunkte: 1. Spirituelles Wohlbefinden 2. Depressivität 3. Angst
Sekundäre Endpunkte: 1. Existentielles Wohlbefinden 2. QoL 3. Hoffnung 4. DHD 5. Selbstwirksam-keitserleben 6. Physisches Wohlbefinden 7. Schmerz
Verwendete Messinstrumente: Depressivität HADS BDI POMS CHADS ESAS
Angst HADS POMS CHADS ESAS
QoL MQoL FACT-B FACIT-Sp EORTC QLQ-C30 EQ-5D QoLC-E FACT-G
Schmerz EORTC QLQ-C30 PRS Einzelitems |
àMA beinhaltet auch nicht-palliative Populationen; Moderatorenanalyse zeigt jedoch keinen Einfluss von "cancer stage" auf relevante Effekte!
1. Depressivität Post-Intervention: 14 RCTs, I2 = 58%; SMD=0.15 [–0.01, 0.32, p >.05] Nach Ausschluss von Studien mit sign. Baseline-Unterschieden (Carlson 2013, 2016, Breitbart 2015, Lloyd-Williams 2013, 2018): 11 RCTs, I2 = 32%; SMD=0.25 [0.10, 0.39, p <.05>
Follow-Up 1 7 RCTs, I2 = 5%; SMD=–0.06 [–0.24, 0.12, p >.05]
Follow-Up 2 3 RCTs, I2 = 55%; SMD=–0.02 [–0.32, 0.28, p >.05]
Follow-Up 3 3 RCTs, I2 = 21%; SMD=–0.04 [–0.23, 0.15, p >.05]
2. Angst Post-Intervention: 13 RCTs, I2 = 71%; SMD=0.12 [–0.08, 0.32, p >.05] Nach Ausschluss von Studien mit sign. Baseline-Unterschieden (Carlson 2013, 2016, Breitbart 2015, Lloyd-Williams 2013, 2018): 11 RCTs, I2 = 64%; SMD=0.21 [0.00, 0.41, p =.05]
Follow-Up 1 7 RCTs, I2 = 29%; SMD=–0.05 [–0.26, 0.16, p >.05]
Follow-Up 2 3 RCTs, I2 = 74%; SMD=0.00 [–0.39, 0.39, p >.05]
Follow-Up 3 3 RCTs, I2 = 71%; SMD=–0.03 [–0.35, 0.30, p >.05]
3. QoL Post-Intervention: 17 RCTs, I2 = 75%; SMD=0.21 [0.01, 0.42, p <.05> Nach Ausschluss von Studien mit sign. Baseline-Unterschieden (Carlson 2013, 2016, Breitbart 2015, Lloyd-Williams 2013, 2018): 16 RCTs, I2 = 74%; SMD=0.21 [0.02, 0.48, p <.05>
Follow-Up 1 8 RCTs, I2 = 45%; SMD=0.18 [–0.06, 0.42, p >.05]
Follow-Up 2 4 RCTs, I2 = 66%; SMD=0.12 [–0.21, 0.45, p >.05]
Follow-Up 3 2 RCTs, I2 = 90%; SMD=0.16 [–0.67, 0.99, p >.05]
4. Schmerz Post-Intervention: 5 RCTs, I2 = 74%; SMD=0.21 [–0.07, 0.49, p >.05]
Follow-Up 1 1 RCTs, I2 = – %; SMD=0.29 [–0.15, 0.72, p >.05]
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Keine der Primärstudien hat systemtisch SUEs erfasst. |
Primärstudien: RCTs mit low RoB SB: 11 PB: nicht erfasst DB: nicht erfasst AB: 16 RB: 14 OB: 18
"Because blinding of participants and personnel is in general not feasible in psychological interventions and outcome assessors were participants themselves, evaluations on these two domains are not provided." (p. 2533)
Review: AMSTAR-2: low quality Method.Mängel in kritischer Domäne 7 non-kritischer Dom. 6,10
Sensitivitäts-analysen: Ausschluss von Studien mit sign. Baselineunter-schieden auf Outcomemaßen (siehe Hauptergebnisse); Ausschluss aller Studien mit hohem Bias-Risiko à keine Ergebnis-veränderung
Publikations-bias: Für MA mit k>10 Studien bestimmt. Asymmetrische Funnel-Plots jedoch keine sign. Egger's Tests bei relevanten Outcomes |
1a |
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Fulton et al. 2018: "Psychotherapy Targeting Depression and Anxiety for Use in Palliative Care: A Meta-Analysis."4
Eingeschlossene Primärstudien: Allen 2004, 2008 Breitbart 2010, 2012 Chochinov 2011 Edelmann 1999a, b Evany 1995 Greer 2012 Hall 2011, 2012 Henry 2010 Juliao 2013 Kissane 2003 Kunik 2007 Lacrombe 1984 Lesperance 2007 Markowitz 1998a, b McLaughlin 2005 Mohr 2000, 2001a,b, 2005a,b, Moorey 1998, Moynihan 1998 Nezu 2003a,b Ransom 2008 Rost 2012 Savard 2006 Speca 2000 Steinhauser 2008 Weiss 2003
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MA
Suchzeitraum: August 2017
Datenbanken: Pubmed PsychInfo Embase CENTRAL
Einschluss-kriterien: P: Erwachsene Pat. In palliativer Behandlung I: Psychotherapie (min. 2 Sitzungen, min 60min.) C: - O: Angst, Depressivität S: RCTs
36 RCTS, N=1536 Patientinnen
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RCTs
Krebs (18) à Subgruppen-analyse durchgeführt! MS (6) HIV (4) Sonst. "life limiting" disease (4) Multiple Diagnosen (4)
Geschlecht: 61% weiblich
Mittleres Alter: 36 - 84
Länder : kA
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Inhalte: Einzeltherapie (23) Gruppentherapie (10) Familientherapie (3)
Davon Face-to-Face (31) Telefon (5)
Dauer/Frequenz/ Länge: 9 Tage-12 Monate (Modalw.=1Monat) 2-23 Sitzungen (M=8.96) 8–208min Sitzungsdauer (M=75.37)
Kontrollgruppen: TAU/UC Warteliste "Social Support" Telefonsupport Problemlöse-training Massage CBT
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Primäre Endpunkte: 1. Depressivität 2. Angst
Sekundäre Endpunkte: 3. QoL
Verwendete Messinstrumente: Depressivität CES-D HADS POMS SCL-90R GDS MADRS BDI HAMD HRSD
Angst HADS POMS STAI SCL-90R BAI HAMA MACS
QoL MQoL FLI EQ-5D FACT-G EORTC QOL-C30 QUAL-E |
1. Depressivität àGesamteffekt: Post-Intervention: 35 RCTs, I2 = 96%; SMD=–0.82 [–1.02, –0.62, p <.001> àModeratorenanalyse: Krebs: Post-Intervention: 17 RCTs, SMD=–0.80, p <.001>
2. Angst àGesamteffekt: Post-Intervention: 21 RCTs, I2 = 89%; SMD=–0.38 [–0.52, –0.24, p <.001> àModeratorenanalyse: Krebs: Post-Intervention: 16 RCTs, SMD=–0.38, p <.001>
3. QoL àGesamteffekt: Post-Intervention: 9 RCTs, I2 = 89%; SMD=0.47 [0.17, 0.78, p <.01> à keine Subgruppenanalyse, aber 7/9 RCTs mit Krebspatient*innen |
Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 4 PB: 8 DB: 4 AB: 11 RB: 14 OB: 5 (Baseline imbalance und Differential attrition)
Review: AMSTAR-2: critically low quality Method. Mängeln in Kritischer Domäne 2, 4, 7, 11 Non-kritischer Dom 1,3,5,10,14
Sensitivitäts-analysen: Starke Heterogenität der Ergebnisse, Durchführung von Moderatorenanalysen (siehe Hauptergebnisse)
Publikations-bias: Funnel-Plot und Regressions-Test à Hinweise auf Bias in Depressivitäts und QoL-Analysen |
1a- |
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Okuyama et al. 2017: "Psychotherapy for depression among advanced, incurable cancer patients: A systematic review and meta-analysis."5
Eingeschlossene Primärstudien: Spiegel 1981 Linn 1982 Wood 1997 Edelmann 1999 Goodwin 2001 Calssen 2001 Savard 2006 Kissane 2007 Henry 2010 Ando 2010 Rost 2012 Breitbart 2012 Greer 2012 |
MA
Suchzeitraum: Bis Juni 2015
Datenbanken: CENTRAL CINHAL Medline Embase PsycInfo mRCT ClinicalTrials.gov ICTRP
Einschluss-kriterien: P: Fortgeschrittener oder terminaler Krebs, Erwachsene I: Psychotherapie (pers. Kontakt) C: - O: min. 1 Depressionsmaß S: RCTs
13 RCTS, N=1294 Patienten
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RCTs
6x metastasierter Brustkrebs 2x Ovarial-karzinom (Stadium III – IV) 5x gemischte fortgeschrittene Tumore
Teilweise mit erhöhter Depressivität als Einschluss-kriterium
Geschlecht: kA
Mittleres Alter: kA
Länder : USA Kanada Japan UK Australien |
Inhalte: 5x Gruppentherapie 2x CBT 2x Sinnbasierte Intervention 1x Beratung 1x PST 1x ACT 1x Lebensrück-schau ("life review")
Länge & Frequenz: Unvollständige Angaben, ca. 60 – 90min Meist wöchentliche Frequenz, Dauer zwischen 2 Sitzungen und einjähriger Gruppenteilnahme
Kontrollgruppen: 4x TAU/UC 2x Warteliste 1x therapeutische Massage 1x Entspannungs-verfahren 1x selbstgeleitete Edukation 3x keine genaue Angabe |
Primäre Endpunkte: 1. Depressivität
Sekundäre Endpunkte: 2. Angst 3. Distress 4. QoL 5. SUEs
Verwendete Messinstrumente: Depressivität BDI POMS SKID
Angst STAI HADS HAMA
Distress POMS GHQ
QoL EORTC QLQ-C30 FACT-G SF-36
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1. Depressivität àGesamteffekt: Post-Intervention: 12 RCTs, n=782 I2 = 83 %; SMD=–0.67 [–1.06, –0.29, p < .001] àGruppentherapie Post-Intervention: 4 RCTs, n=403 I2 = 85 %; SMD=–0.74 [–1.29, –0.19, p = .008] àEinzeltherapie: Post-Intervention: 8 RCTs, n=379 I2 = 84%; SMD=–0.62 [–1.19, –0.05, p = .03] à"Hochdosiert": Post-Intervention: 9 RCTs, n=682 I2 = 77%; SMD=–0.60 [–0.94, –0.26, p < .001] à"Niedrigdosiert": Post-Intervention: 3 RCTs, n=100 I2 = 90%; SMD=–0.76 [–2.39, 0.88, p = .36] àMethodisch hochwertig (low RoB: Post-Intervention: 6 RCTs, n=459 I2 = 89%; SMD=–0.81 [–1.45, –0.17, p = kA] àdurchgeführt als Sensitivitätsanalyse
2. Angst àGesamteffekt: Post-Intervention: 11 RCTs, n=676 I2 = 82%; SMD=–0.65 [–1.05, –0.26, p = .001]
3. Distress àGesamteffekt: Post-Intervention: 7 RCTs, n=526 I2 = 91%; SMD=–1.02 [–1.70, –0.35, p = .003]
4. QoL àGesamteffekt: Post-Intervention: 3 RCTs, n=138 I2 = 91%; SMD=0.17 [–0.16, 0.51, p = .31]
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Keines der eingeschlos-senen RCTs berichtet SUEs |
Primärstudien: RCTs mit low RoB SB: 4 PB: 0 DB: 2 AB: 6 RB: 0 OB: kA
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 7,11, non-kritischer Dom. 1,8,
Sensitivitäts-analysen: Durchgeführt (siehe Hauptergebnisse)
Starke Heterogenität der Ergebnisse / nicht durch Subgruppen-analysen erklärbar
Publikations-bias: Visuelle Prüfung des Funnel-Plot liefert keine Hinweise |
1a |
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Poort et al. 2017: "Psychosocial interventions for fatigue during cancer treatment with palliative intent."6
Eingeschlossene Primärstudien: Armes 2007 Barsevick 2004 Barsevick 2010 Bordeleau 2003 Bruera 2013 Chan 2011 Classen 2001 Edelman 1999 Johansson 2008 Savard 2006 Sharpe 2014 Spiegel 1981 Steel 2016 Walker 2014 |
Cochrane Review
Suchzeitraum: Bis November 2016
Datenbanken: CENTRAL CINHAL Medline PsycInfo Embase
Einschluss-kriterien: P: unheilbare Krebserkrankte in palliativer Behandlung I: psychosoziale Intervention C: UC oder nicht-psychosoziale Kontrolle O: Fatigue S: RCTs
14 RCTs, N=3077 Patienten
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RCTs
6x unheilbare Krebserkrankung 8x gemischt
Geschlecht: 17% - 90% weiblich
Mittleres Alter: 50 - 64
Länder : USA China Kanada UK Australien Schweden |
Inhalte: 5x CBT 3x supportiv-expressive Gruppentherapie 2x"energy conservation" + Aktivität + Schlafmanagement 4x sonstige
Länge & Frequenz: 2 Wochen – 12 Monate
Kontrollgruppen: 9x TAU/UC 3x attentional control 2xselbstgeleitete Edukation
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Primäre Endpunkte: 1. Fatigue
Verwendete Messinstrumente: Fatigue POMS EORTC QLQ-C30 FACIT-F FACT-F PFS-Revised MFI |
1. Fatigue Post-Intervention: 12 RCTs, n= 535 I2 = 43%; SMD=–0.25 [–0.50, 0.00, p =.05] GRADE: very low
Follow-up 1 (3 Wochen – 6 Monate): 4 RCTs, n=147 I2 = 0%; SMD=–0.66 [–1.00, –0.32, p < .001] GRADE: very low
Follow-up 2 (9 Wochen – 18 Monate): 2 RCTs, n=91 I2 = 29%; SMD=–0.41 [–1.12, 0.30, p = .26] |
In 3/14 Studien berichtet |
Primärstudien: RCTs mit low RoB SB: 5 PB: nicht erhoben DB: 5 AB: 8 RB: 13 OB: -
Review: AMSTAR-2: high quality Method.Mängel in kritischer Domäne - non-kritischer Dom. 1
Sensitivitäts-analysen: Ausschluss von 3 Studien mit n<10 Patienten pro Treatment-Arm à keine Veränderung der Ergebnisse
Publikations-bias: visuelle Inspektion des Funnel-Plot liefert keine Hinweise |
1a |
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Wang et al. 2017: "The effects of life review interventions on spiritual well-being, psychological distress, and quality of life in patients with terminal or advanced cancer: A systematic review and meta-analysis of randomized controlled trials."7
Eingeschlossene Primärstudien: Ando 2010 Hall 2011 Henry 2010 Chochinov 2011 Mok 2012 Xiao 2013 Juliao 2013, 2014 Breitbart 2012 |
MA
Suchzeitraum: Bis Februar 2017
Datenbanken: CENTRAL CINHAL Pubmed PsycInfo Web of Science Einschluss-kriterien: P: Fortgeschrittener oder terminaler Krebs, Erwachsene I: therapeutisches "Life Review", Einzelsetting C: Placebo oder nicht-psychologisch O: Spirituelles Wohlbefinden, Distress, QoL S: RCTs
8 RCTS, N=955 Patienten
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RCTs
5x Krebspatienten in palliativer Betreuung 3x fortgeschrittene Krebserkrankung (Stadium III o. IV)
Geschlecht: kA
Mittleres Alter: 54 - 66
Länder : USA China Kanada Japan UK Portugal |
Inhalte: Therapeutische Lebensrückschau ("life review")
Länge & Frequenz: 15-60min/Sitzung, 1-7 Sitzungen,
Kontrollgruppen: 7x TAU/UC 1x therapeutische Massage
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Primäre Endpunkte: 1. Spirituelles Wohlbefinden 2. Depressivität 3. Angst 4. Distress 5. QoL
Verwendete Messinstrumente: Depressivität HADS
Angst HADS
Distress HADS
QoL Einzelitems EQ-5D QoLC-E MQoL |
1. Depressivität Post-Intervention: 4 RCTs, n= 347 I2 = 0%; SMD=–0.09 [–0.30, 0.12, p =.42]
Follow-up (2 Wochen – 3 Monate): 3 RCTs, n=109 I2 = 0%; SMD=0.07 [–0.31, 0.44, p = .73]
2. Angst Post-Intervention: 4 RCTs, n=347 I2 = 0%; SMD=0.11 [–0.10, 0.33, p =.29]
Follow-up (2 Wochen – 3 Monate): 3 RCTs, n=109 I2 = 0%; SMD=–0.04 [–0.42, 0.33, p = .82]
3. Distress Post-Intervention: 3 RCTs, n=311 I2 = 93%; SMD=–0.32 [–0.55, –0.09, p =.007] à nach Entfernung von Ando 2010, keine sign. Unterschiede und l²=0%
Follow-up (2 Wochen – 3 Monate): 1 RCTs, n=24 I2 = na ; SMD=–0.26 [–1.06, 0.54, p = .53]
4. QoL àEinzelitems: Post-Intervention: 4 RCTs, n=384 I2 = 92%; SMD=0.35 [0.15, 0.56, p <.001>
Follow-up (2 Wochen – 3 Monate): 3 RCTs, n=146 I2 = 90 ; SMD=0.82 [0.47, 2.28, p <.001> à nach Entfernung von Xiao 2013, keine sign. Unterschiede und l²=0% zu beiden Zeitpunkten
àValidierte FraBö: Post-Intervention: 4 RCTs, n=286 I2 = 0%; SMD=0.25 [–0.03, 0.54, p =.08] Follow-up: 4 RCTs, n=167 I2 = 0%; SMD=0.16 [–0.15, 0.46, p = .31]
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Keines der eingeschlos-senen RCTs berichtet SUEs |
Primärstudien: RCTs mit low RoB SB: 5 PB: nicht erhoben DB: 2 AB: 1 RB: 5 OB: 2
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 2,7,15, non-kritischer Dom. 10,12
Sensitivitäts-analysen: Effekte robust gegenüber Entfernung jeweils einer Studie (Ausnahmen siehe Hauptergebisse)
Publikations-bias: aufgrund geringer Studienzahl (<10) pro Meta-Analyse nicht geprüft |
1a |
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Teo et al. 2019: "Psychosocial interventions for advanced cancer patients: A systematic review."8
Eingeschlossene Primärstudien: Insg. 68 Primärstudien, davon 11x sinnbasierten Interventionen: Breitbart 2010, 2012, 2015, 2108 Butler 2009 Hansen 2009 Henry 2010 Kissane 2007 Lo 2016 Piderman 2014 Spiegel 2007
9x würde-basierten Interventionen & Lebensrückschau Ando 2010 Chochinov 2011 Hall 2011 Juliao 2014 Lloyd Williams 2018 Mok 2012 Vuksanovic 2016 Xiao 2013
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SysRev
Suchzeitraum: Januar 2007 bis Juni 2018
Datenbanken: SCOPUS CINHAL Medline PsycInfo
Einschluss-kriterien: P: erwachsene Krebspatienten, min. 70% Stadium III -IV I: psychosoziale Intervention C: - O: - S: RCTs
68 RCTs
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Die folgenden Angaben beziehen sich auf die beiden relevanten Subgruppen!
RCTs
Populationen: 16x gemischte Krebsdiagnosen 3x Brustkrebs 1x Ovarialkarzinom
Alle Populationen entweder: Stadium III – IV, in Palliativversor-gung, mit LE <5 Jahren
Geschlecht: kA
Mittleres Alter: kA
Länder : USA (7) Kanada (2) Australien (2) UK (3) Portugal (1) China (1) Japan (1) Multinational (1)
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Inhalte: 20x CBT basiert 11x sinnbasierte Interventionen 9x würdebasiert, Lebensrückschau 7x sonstige Beratung 11x edukative Interventionen, unidirektional 10x Musiktherapie, therp. Schreiben und sonstiges
Dauer/Frequenz/ Länge: 25 – 90min 1 – 52 Termine 2 Wochen – 12 Monate Meist wöchentliche Termine
Kontrollgruppen: 11x TAU/UC 2x Warteliste 3x Edukation 2x Supportive Therapie 1x therapeutische Massage 1x Entspannung
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Endpunkte: Keine Aufschlüsselung nach Outcomemaß
u.a. Spirituelles Wohlbefinden, Sinnempfinden, QoL, Schmerz, "Suffering", Überlebensrate, Distress, Würde, Generativität, Ego-Integrität
Verwendete Messinstrumente: kA |
1. Sinnbasierte Interventionen 9/11 RCTs mit ausreichend. statistischer Power
6/9 Verbesserung auf mind. einem primären Outcome
2. Würdebasierte Interventionen & Lebensrückschau 5/9 RCTs mit ausreichend. statistischer Power
4/5 Verbesserung auf mind. einem primären Outcome
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Keine SUEs berichtet |
Primärstudien: RCTs mit low RoB SB: 14 PB: 0 DB: 3 AB: unklar RB: unklar OB: unklar
Review: AMSTAR-2: critically low quality Method.Mängel in kritischer Domäne 7,13 non-kritischer Dom. 8,10,14
Sensitivitäts-analysen: Keine MA
Publikationsbias: Nicht diskutiert |
1a-
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Spezifische psychoonkologische Interventionen in der Palliativphase RCTs (2015 – 2020)
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Referenz/ (Autor, Jahr, Journal) |
Studientyp |
Patienten-merkmale |
Interventionen |
Untersuchte Endpunkte |
Hauptergebnisse |
Neben-/ Wechselwirkungen |
Finanzierung / Conflict of Interest |
Methodische Bemerkungen |
Evidenzklasse |
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Unterstützende Evidenz (7/13) |
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Poort (2020): Cognitive behavioral therapy or graded exercise therapy compared with usual care for severe fatigue in patients with advanced cancer during treatment: a randomized controlled trial. |
RCT prospektiv, multizentrisch, offen, 3 Arme
Randomisiert: N = 134 Post-Treatment: N = 126 Follow-Up1: Follow-Up2: N = 112
ITT-Ansatz mit multipler Imputation; ausgewertet: N=126
Land: Niederlande
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Krebspatienten in der Palliativphase (versch. Krebs-diagnosen)
Geschlecht: 57% weiblich
Alter: 34-85 M = 62.76
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Arm A: NR=45 NP=43 NFU1=39 NFU2=39 KVT, 10x 1h Sitzungen, über 12 Wochen
Arm B: NR=34 NP=40 NFU1=36 NFU2=33 GET (graded exercise therapy) Bis zu 2x 2h Training pro Woche, über 12 Wochen
Arm C: NR=46 NP=43 NFU1=42 NFU2=40
CAU
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Erhebungszeitpunkt Baseline Post-Treatment (2 Wochen) Follow-Up1 (6 Wochen) Follow-Up2 (24 Wochen)
Primäre Endpunkte: 1. Fatigue (CIS, EORTC-QLQ-C30)
Sekundäre Endpunkte: 1. QoL (EORTC-QLQ-C30) 2. Fatigue-bezogene Behinderung (SIP8) |
1. Fatigue à KVT vs. CAU Post-Treatment: Sign. Unterschied zugunsten von KVT (CIS: d=0.7; EORTC: d=0.6)
2. QoL à KVT vs. CAU Post-Treatment: Sign. Unterschied zugunsten von KVT (d=0.4) |
Arm A: KVT SUEs: kA UEs: kA
Arm B: GET SUEs: kA UEs: kA
Arm C: CAU SUEs: kA UEs: kA
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Dutch Cancer Society
Laut Angaben kein COI
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Risk of Bias
SB1: low SB2 low PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N=219) nicht erreicht
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Rodin (2020): Emotion And Symptom-focused Engagement (EASE): a randomized phase II trial of an integrated psychological and palliative care intervention for patients with acute leukemia. |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 42 Mid-Intervention: N = 32 Post-Intervention: N = 29 Follow-Up1: N = 32
ITT-Analyse mit multilevel Modeling
Land: Kanada 2015 - 2016
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Neudiagnostizierte oder neurezidivierte Akute myeloische Leukämie oder akute lymphatische Leukämie
Geschlecht: 38.1 % weiblich
Alter: 19-74 Mittelwert: 52.86 |
Arm A: NR=22 Nm=14 Np=13 NFU1=13
EASE (Emotion and Symptom Focused Engagement) EASE-Psy: 8 Wochen, 8-12 Sitzungen, 30-60 Minuten EASE-phys: systematisches Symptom Screening mit ggf. auslösender Frühpalliativ-versorgung
Arm B: NR=20 Nm=18 Np=16 NFU1=19 CAU |
Erhebungszeitpunkt Baseline Mid-Intervention (4 Wochen) Post-Intervention Follow-Up (4 Wochen)
Primäre Endpunkte: 1. Traumatische Stress-symptome (SASRQ)
Sekundäre Endpunke: 2. Körperliche Symptome (MSAS) 3. Schmerz (BPI) 4. QoL 5. Depressivität (BDI-II) Zufriedenheit (FAMCARE-P16) |
1. Distress à EASE vs. CAU keine sign. Unterschiede zu keinem Zeitpunkt
2. Schmerz (Intensität) à EASE vs. CAU Mid- & Post-Intervention: Keine sign. Unterschiede
Follow-Up: Sign. Unterschiede zugunsten von EASE
3. QoL àEASE vs. CAU Keine sign. Unterschiede zu keinem der Zeitpunkte
4. Depressivität àEASE vs. CAU Keine sign. Unterschiede zu keinem der Zeitpunkte
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Arm A: EASE SUEs: 0/22 UEs: kA
Arm B: CAU SUEs: 0/20 UEs: kA |
Canadian Cancer Society Research Institute + Princess Margaret Cancer Centre and Princess Margeret Cancer Foundation
„AS reports personal fees and grants outside this submitted work from Novartis, Takeda Pharmaceuticals,Otsuka Pharmaceutical, Jazz Pharmaceuticals,Medivir,and Abbvie.“ (p.176)
Restliche Autoren geben keinen COI an
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Risk of Bias
SB1: low SB2 low PB: high DB: high AB: low RB: low
Geplante Fallzahl (N=50) nicht erreicht
Phase-2-Studie
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Breitbart et al., 2018: Individual Meaning-Centered Psychotherapy for the Treatment of Psychological and Existential Distress: A Randomized Controlled Trial in Patients With Advanced Cancer |
RCT prospektiv, monozentrisch, offen, 3 Arme
Randomisiert: N=321 Mid-Intervention: N=219 Post-Intervention: N=207 Follow-Up: N=177
ITT-Ansatz; ausgewertet N=321
Land: USA März 2011 - März 2016 |
Krebspatient*innen (Stage IV)
55 x Lungenkrebs, 47 x Bauchspeicheldrüsenkrebs, 45 x Eierstockkrebs, 43 x Brustkrebs, 40 x Kolon/Rektal
Geschlecht: 72% weiblich
Alter: 25-85 Mittelwert: 58 |
Arm A: NR=109 Nm=82 Np=78 NFU=70 "Individual meaning-centered Psychotherapy" (IMCP), wöchentlich, 7 Sitzungen
Arm B: NR=108 Nm=74 Np=70 NFU=54 Supportive Psycho-therapie (SP), wöchentlich, 7 Sitzungen
Arm C: NR=104 NP=63 NFU1=59 NFU2=53 Enhanced Usucal care (EUC)
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Erhebungszeitpunkt Baseline Mid-Intervention (4 Wochen) Post-Intervention Follow-Up (16 Wochen)
Primäre Endpunkte: 1. Spirituelles Wohlbefinden (SWB) 2. Individuelles Sinnerleben (LAP-R) 3. QoL (MQOL)
Sekundäre Endpunkte: 1. Hoffnungslosigkeit (HAI) 2. Einstellung zu beschleunigten Ableben (SAH-D) 3. Angst 4. Depressivität |
Hauptergebnisse während Palliativbehandlung
Zeit x Gruppe Interaktionseffekte:
1. QoL à SP vs. IMPC vs. EUC Sign. stärkere Verbesserung in IMPC vs. SP und IMPC vs. EUC.
2. Angst à SP vs. IMPC vs. EUC Sign. stärkere Angstreduktion in IMPC vs. SP. Sign. stärkere Angstreduktion in IMPC und SP vs. EUC
3. Depressivität à SP vs. IMPC vs. EUC Sign. stärkere Reduktion der Depressivität in IMPC vs. SP. Keine sign. Unterschiede in Vergleichen IMPC vs. EUC und SP vs. EUC
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Keine Angaben zu UEs |
National Cancer Institute (R01 CA128134, P30 CA008748).
Laut Angaben kein COI |
Risk of Bias
SB1: unclear SB2 unclear PB: high DB: high AB: low RB: high
Geplante Fallzahl (N=312) erreicht
Obwohl Post-hoc-Analysen keinen Unterschied in den Behandlungseffekten zwischen Männern und Frauen ergaben, sind weitere Untersuchungen zu dieser möglichen Quelle der Verzerrung (bias) gerechtfertigt. |
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Rodin (2018): Managing Cancer and Living Meaningfully (CALM): A Randomized Controlled Trial of a Psychological Intervention for Patients With Advanced Cancer. |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 305 Post-Intervention: N =248 Follow-Up N =227
ITT-Ansatz (mit multipler Imputation als Sensitivitäts-analyse): ausgewertet N=165-247 (je nach Outcome und Erhebungszeitpunkt)
Land: Kanada 2012-2016 |
Verschiedene Krebserkrankungen im fortgeschrittenen Stadium, inoperable Tumore, aggressive Tumorarten
Geschlecht: 60% weiblich
Alter: Mittelwert: 59.1 |
Arm A: NR=151 NP=119 NFU1=107 CALM (Managing Cancer and Living Meaningfully) 3-6 Sitzungen innerhalb von 3-6 Monaten; jeweils 45-60 Minuten
Arm B: NR=154 NP=129 NFU1=120 CAU
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Erhebungszeitpunkt Baseline Post-Intervention Follow-Up (12 Wochen)
Primäre Endpunkte: 1. Depressivität
Sekundäre Endpunkte: 1. Depression (SKID) 2. Generalisierte Angst (GAD-7) 3. Todesangst (DADDS) 4. Spirituelles Wohlbefinden (FACIT-Sp-12) 5. QoL am Lebensende 6. Erfahrungen in engen Beziehungen (ECR-M16) 7. Paarkommunikation (CCS) 8. Posttraumatisches Wachstum (PTGI) 9. Demoralisierung (DS)
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1. Depressivität à CALM vs. CAU Post-Intervention: Sign. Unterschiede zugunsten von CALM (d=0.23)
Follow-Up: Sign. Unterschiede zugunsten von CALM (d=0.29)
2. Angst à CALM vs. CAU
3. Todesangst à CALM vs. CAU Keine sign. Unterschiede zu keinem der Zeitpunkte
4. QoL am Lebensende à CALM vs. CAU 3 Subskalen: Vorbereitung auf das Lebensende: Beziehung zum Gesundheitsdienstleister: Lebenserfüllung: Keine sign. Unterschiede zu keinem der Zeitpunkte.
|
Arm A: CALM SUEs: 0/151 UEs: 0/151
Arm B: CAU SUEs: 0/154 UEs: 0/154 |
Canadian Institutes of Health Research + Princess Margaret Cancer Centre
Laut Angaben kein COI |
Risk of Bias
SB1: low SB2 low PB: high DB: high AB: low RB: low
Geplante Fallzahl (N=242) teilweise erreicht (für uns interessierende Outcomes nur erreicht für Depressivität Post-Treatment)
|
|
||||||||
|
Wells-Di Gregorio (2018): Pilot randomized controlled trial of a symptom cluster intervention in advanced cancer. |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 28 Post-Treatment: N = 21
ITT-Ansatz, kA zu Imputation ; ausgewertet. N=28
Land: USA kA des Zeitraums |
Fort-geschrittener Krebs (< 55% 5-Jahres Überlebens-wahrscheinlichkeit)
Geschlecht: 82% weiblich
Alter: M = 56.54 |
Arm A: NR=17 NP=14 FOCUS (Finding our center under stress) 3x 1,5 h (2x face-to-face, 1x DVD), über 6 Wochen
Arm B: NR=11 NP=7 WL (6 Wochen) |
Erhebungszeitpunkt Baseline Post-Treatment
Primäre Endpunkte: 1. Schlafprobleme 2. Sorgen (PSWQ) 3. Depressivität (CES-D)
Sekundäre Endpunkte 4. Unsicherheits-intoleranz (IUS) 5. Schläfrigkeit (ESS) 6. Angst (STAI) 7. Fatigue (FSI) 8. Distress (JSCS) Hyperarousal (IES-R) |
1. Depressivität à FOCUS vs. WL Sign. Reduktion der Depressivität zugunsten von FOCUS nach 6 Wochen (d=-0.88)
2. Angst à FOCUS vs. WL Keine sign. Unterschiede nach 6 Wochen
3. Fatigue à FOCUS vs. WL Keine sign. Unterschiede nach 6 Wochen
4. Distress à FOCUS vs. WL Sign. Reduktion des Distress zugunsten von FOCUS nach 6 Wochen (d=-0.83) |
Arm A: FOCUS SUEs: kA UEs: kA
Arm B: WL SUEs: kA UEs: kA
|
Lance Armstrong Foundation Survivorship Center for Excellence Grant + Tzagournis Medical Research Endowment Fund + National Center for Advancing Tranlational Sciences Grant + American Cancer Society Institutional Seed
kA bzgl. COI |
Risk of Bias
SB1: unclear SB2 unclear PB: high DB: high AB: low RB: low
Pilotstudie
Geplante Fallzahl (N=34) nicht erreicht
|
|
||||||||
|
Onyechi (2016): Effects of Rational-Emotive Hospice Care Therapy on Problematic Assumptions, Death Anxiety, and Psychological Distress in a Sample of Cancer Patients and Their Family Caregivers in Nigeria. |
RCT, prospektiv,monozentrisch, offen, 2 Arme
Randomisiert: N=32 (Patienten)/N=52 (Caregivers) Post-Intervention : N=32 (Patienten)/ N=52 (Caregivers) Follow-Up :
ITT-Ansatz Ausgewertet: N=32 (Patienten)/ N=52 (Caregivers)
Land: Nigeria 2014-2015 |
Krebspatienten (gemischt) im Endstadium und pflegende Angehörige
Geschlecht: Patienten: 87.5% weiblich Angehörige: 84.6% weiblich
Alter: Patienten: M = 48.3 Angehörige: M = 55.8
|
Arm A: NR=16 (Patienten)/26 (Caregivers) NP=16 (Patienten)/26 (Caregivers) NFU=16 (Patienten)/26 (Caregivers)
REHCT (rational emotive Therapie in Palliativbegleitung) Wöchentliche Hausbesuche à 45 Minuten über 10 Wochen + 4 Wochen follow-up Besuche
Arm B: CAU NR = 16 (Patienten)/26 (Caregivers) NP=16 (Patienten)/26 (Caregivers) NFU=16 (Patienten)/26 (Caregivers)
Unspezifische wöchentliche Hausbesuche à 45 Minuten über 10 Wochen + 4 Wochen follow-up Besuche |
Erhebungszeitpunkte: Baseline Post-Intervention Follow-Up (4 Wochen)
Primäre Endpunkte: 1. Annahmen (CPFCAQ) 2. Todesangst (DAQ) 3. Distress
|
Patientenoutcomes
1. Todesangst à REHCT vs. CAU Post-Intervention und Follow-Up: Sign. Gruppenunterschiede zugunsten von REHCT (partielles Eta²= 0.97 bzw. 0.99)
2. Distress à REHCT vs. CAU Post-Intervention und Follow-Up: Sign. Gruppenunterschiede zugunsten von REHCT (partielles Eta²= 0.98 bzw. 0.99) |
Arm A: REHCT UEs: kA
Arm B: CAU SUEs: kA |
Keine Angaben zur Finanzierung
Laut Angaben kein COI |
Risk of Bias
SB1: high SB2: high PB: high DB: high AB: low RB: unclear
Keine Fallzahlplanung |
|
||||||||
|
Breitbart et al., 2015: Meaning-Centered Group Psychotherapy: An Effective Intervention for Improving Psychological Well-Being in Patients With Advanced Cancer
|
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N=253 Post-Intervention: N=127 Follow-Up: N=102
ITT-Ansatz ohne Imputation: ausgewertet N=253
Land: USA
|
Fortgeschrittener Krebs (Stage III-IV)
40 x Lungenkrebs, 45x Bauchspeicheldrüsenkrebs, 75 x Brustkrebs,
|
Arm A: NR=132 NP=69 NFU1=57 MCGP, sinnbasierte Gruppen-psycho-therapie, 8 Wochen, 1x wöchentlich, absolvierte Sitzungen M=5.55, SD=2.3
Arm B: NR=121 NP=58 NFU1=45 SGP, supportive Gruppen-psycho-therapie, 8 Wochen, 1x wöchentlich, absolvierte Sitzungen M=5.28, SD=2.3
|
Erhebungszeitpunkt Baseline Post-Intervention Follow-Up (8 Wochen)
Primäre Endpunkte: 1. geistiges Wohlbefinden (SWB) 2. QoL (allgemeine Lebensqualität; MQOL)
Sekundäre Endpunkte: 1. Depressivität (BDI) 2. Hoffnungslosigkeit (HAI) 3. Wunsch nach beschleunigtem Tod (SAHD) 4. Angst (HADS-A) 5. körperliche Symptom-Belastung (MSAS-GDI) |
Prä-Post-2 Follow-Up: Sign. Haupteffekte für Gruppe (MCGP geht es zu Baseline "schlechter") und Zeit (Besserung über Zeit), auf allen rel. Variablen.
Zeit x Gruppe Interaktionseffekte:
1. QoL à MCGP vs. SGP Sign. stärkere Verbesserung der Lebensqualität in MCGP
2. Depressivität à MCGP vs. SGP Sign. stärkere Reduktion der Depressivität in MCGP
3. Angst à MCGP vs. SGP Keine sign. Zeit x Gruppe Interaktion
|
Keine Angaben zu UEs |
Memorial SloanKettering Cancer Center, New York,
Laut Angaben kein COI |
Risk of Bias
SB1: unclear SB2 unclear PB: high DB: high AB: low RB: unclear
Geplante Fallzahl (N=252) erreicht
|
|
||||||||
|
Keine Hinweise für höhere Wirksamkeit des Treatments (6/13) |
|||||||||||||||||
|
Nordly (2018): Systematic fast-track transition from oncological treatment to dyadic specialized palliative home care: DOMUS – a randomized clinical trial. |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 340 Follow-Up1 : N=269 Follow-Up2 : N =251 Follow-Up3: N =223 Follow-Up4: N = 148
ITT-Ansatz; Verstorbene Pat. aus Analyse der Folgezeitpunkte ausgenommen; Multiple Imputation von fehlenden Werten durch Nicht-Antwort als Sensitivitäts-analyse; ausgewertet : N=144-268 (je nach Outcome und zeitpunkt)
Land: Dänemark 2013 - 2016 |
Unheilbarer Krebs (keine weiteren Behandlungsmöglichkeiten o. Behandlung wird abgelehnt)
Geschlecht: 51 % weiblich
Alter: Mittelwert: 67
|
Arm A: NR=170 NFU1=139 NFU2=135 NFU3=120 NFU4=80 DOMUS, dyadische psychologische Intervention (exitenziell-phänomenologische Therapie) ; min. 2 Sitzungen im ersten Monat + weitere Sitzungen nach Bedarf + häusliche Palliativversorgung
Arm B: NR=170 NFU1=130 NFU2=116 NFU3=103 NFU4=68 CAU
|
Erhebungszeitpunkt Baseline Follow-Up1 (2 Wochen) Follow-Up2 (4 Wochen) Follow-Up3 (8 Wochen) Follow-Up4 (24 Wochen)
Primäre Endpunkte: 1. Ort des Todes
Sekundäre Endpunkte: 2. QoL (EORTC) - global 3. Angst (HADS) Depressivität (HADS) |
1. QoL (global) à DOMUS vs. CAU
2. Angst à DOMUS vs. CAU Keine sign. Unterschiede zu den untersuchten Zeitpunkten
3. Depressivität à DOMUS vs. CAU Keine sign. Unterschiede zu den untersuchten Zeitpunkten |
Arm A: DOMUS SUEs: 0/170 UEs: 0/170
Arm B: CAU SUEs: 0/170 UEs: 0/170 |
Danish Cancer Society + TrygFonden
Laut Angaben kein COI |
Risk of Bias
SB1: low SB2 low PB: high DB: high AB: high RB: high
Geplante Fallzahl (N=340) nicht erreicht (?) à AutorInnen beschreiben Studie als underpowered
|
|
||||||||
|
Serfaty (2019a): Acceptance and commitment therapy for adults with advanced cancer (CanACT): A feasibility randomised controlled trial. |
RCT prospektiv, monozentrisch, offen, 2 Arme
Randomisiert: N = 42 Follow-Up1 : N = 24 Follow-Up2 : N = 18 Follow-Up3 : N = 14 Follow-Up4 : N = 15
Kein ITT ; Ausgewertet : N=30
Land: UK 2015-2016
|
Fortgeschrittener Krebs, unheilbar
Geschlecht: 74% weiblich
Alter: M = 62
|
Arm A: NB = 20 NFU1=8 NFU2=7 NFU1=7 NFU2=7 ACT; 8 wöchentliche Sitzungen à max. 1h
Arm B: NB = 22 NFU1=16 NFU2=11 NFU1=7 NFU2=8 AC, talking control (TC), 8 wöchentliche Sitzungen à max. 1h
|
Erhebungszeitpunkt Baseline Follow-Up1 (6 Wochen) Follow-Up2 = Post Intervention (12 Wochen) Follow-Up3 (18 Wochen) Follow-Up4 (24 Wochen)
Primäre Endpunkte: 1. QoL
Sekundäre Endpunkte: 2. Distress (K-10) 3. Körperliche Funktion ACT-Prozesse |
1. QoL à ACT vs. TC Follow-Up2: keine sign. Gruppenunterschiede; Keine inferenzstatistische Auswertung zu anderen Zeitpunkten
2. Distress à ACT vs. TC Follow-Up2: keine sign. Gruppenunterschiede; Keine inferenzstatistische Auswertung zu anderen Zeitpunkten |
Arm A: ACT SUEs: kA UEs: kA
Arm B: TC SUEs: kA UEs: kA
|
National Institute for Health Research (NIHR) (UK) + Marie Curie core grant funding
Laut Angaben kein COI
|
Risk of Bias
SB1: low SB2 low PB: high DB: high AB: high RB: low
Phase-2-Studie
Keine Fallzahlplanung |
|
||||||||
|
Serfaty (2019b): Manualised cognitive–behavioural therapy in treating depression in advanced cancer: the CanTalk RCT. |
RCT prospektiv, multizentrisch, single-blind, 2 Arme
Randomisiert: N = 230 Mid-Treatment: N=168 Post-Treatment: N=148 Follow-Up1 : N=134 Follow-Up2 : N=130
ITT-Ansatz; Ausgewertet: N = 185
Land: UK 2012 - 2015 |
Krebspatienten in der Palliativphase mit DSM-IV Diagnose Depression
Geschlecht: 66.1 % weiblich
Alter: 27-93 M = 59.5
|
Arm A: KVT NB = 115 NM=86 NP=69 NFU1=63 NFU2=65 12 Sitzungen über 3 Monate
Arm B: TAU NB = 115 NM=82 NP=79 NFU1=71 NFU2=65
|
Erhebungszeitpunkt Baseline Mid-Treatment (6 Wochen) Post-Treatment Follow-Up1 (6 Wochen Follow-Up2 (12 Wochen)
Primäre Endpunkte: 1. Depressivität (BDI-II)
Sekundäre Endpunkte: 2. Depressivität (PHQ-9) 3. Kosteneffektivität (EuroQoL-5) 4. Zufriedenheit 5. Körperliche Funktion 6. Client Service Receipt Inventory (CSRI)
|
1. Depressivität à KVT vs. TAU Keine sign. Unterschiede zu den untersuchten Zeitpunkten
(Subgruppenanalyse: Sign. Vorteil von KVT bei getrennten, geschiedenen oder verwitweten Probanden) |
Arm A: KVT SUEs: 2/115 UEs: 0/115
Arm B: TAU SUEs: 3/115 UEs: 0/115
SUEs = Klinikeinweisung, Todesfall |
National Institute for Health Research Research Health Technology Assessment Programme (UK)
Marc Serfaty ist Mitglied des Vorstands des National Institute for Health Research Health Technology Assessment |
Risk of Bias
SB1: low SB2 low PB: high DB: high AB: low RB: low
Geplante Fallzahl (N=240) nicht erreicht
|
|
||||||||
|
Kleijn et al., (2018): The efficacy of Life Review Therapy combined with Memory Specificity Training (LRT-MST) targeting cancer patients in palliative care: A randomized controlled trial |
RCT prospektiv, multizentrisch, offen, 2 Arme
Randomisiert: N=107 Post-Treatment: N=91 Follow-Up: N=77 ITT-Ansatz ohne Imputation; Ausgewertet: N=77
Land: Niederlande Juni 2010 – Dezember 2013 |
Fortgeschrittener/ unheilbarer Krebs (Stadium III bis IV)
66 x Lungenkrebs 23 x Blutkrebs 2 x Kopf- und Halskrebs 5 x Brustkrebs 11 x Andere Krebsarten
Geschlecht: 46.7% weiblich
Alter: 31-86 Mittelwert: 62 |
Arm A: NR=55 NP=45 NFU1=38 LRT-MST: Lebensrückschau mit Training des autobiografischen Gedächtnisses, 4 Wochen, 1x wöchentlich, 60 Minuten
Arm B: NR=52 NP=47 NFU1=39 WL
|
Erhebungszeitpunkt Baseline Post-Treatment Follow-Up (4 Wochen)
Primäre Endpunkte: 1. Ich-Integrität und Verzweiflung (NEIS).
Sekundäre Endpunkte: 2. Distress (HADS), 3. QoL (EORTC QLQ-PAL15) 4. Spezifität des Autobiographischen Gedächtnisses (AMT). |
1. Distress à LRT-MST vs. WL Post-Intervention und Follow-Up: Keine sign. Zeit-Gruppe-Interaktion
2. QoL à LRT-MST vs. WL: Post-Intervention und Follow-Up: Keine sign. Zeit-Gruppe-Interaktion
|
Keine Angaben zu UEs |
Die Niederländische Organisation für Gesundheitsforschung und Entwicklung [Förderungsnummer: 11510003]. Der Geldgeber hatte keinen Einfluss auf das Studiendesign, die Datenerhebung und -analyse.
Laut Angaben keine COI
|
Risk of Bias
SB1: low SB2 low PB: high DB: high AB: unclear RB: high
Keine genauen Angaben zu Verzerrungen
Geplante Fallzahl (N=90) nicht erreicht |
|
||||||||
|
Azuero et al., 2017: Brief depression literacy intervention with palliative cancer outpatients
|
RCT prospektiv, monozentrisch offen, 2 Arme
Randomisiert: N=43 Follow-Up: N=40
Kein ITT; ausgewertet: N=40
Land: USA 2014 - 2015 |
Depressive Krebspatient*innen in ambulanter palliativer Versorgung (12 x Brustkrebs 7 x Gebärmutterhalskrebs 5 x Kopf/Halskrebs 19 x Andere Krebsformen)
Geschlecht: 75% weiblich
Alter: 37-59 Mittelwert: 48.2 |
Arm A: NR=21 NFU=18 Psycho-edukative Intervention (IMPACT) zu Depressivität und Krebs, einmalig 60min
Arm B: NR=22 NFU=22 TAU
|
Erhebungszeitpunkt Baseline Follow-Up (ca. 4 Wochen (Range: 23-153 Tage ab Baseline)
Primäre Endpunkte: 1. Depressivitäts-wissen
Sekundäre Endpunkte: 2. Distress 3. Somatische Beschwerden (SPHERE) 4. Psychische Beschwerden 5. (SPHERE) |
|
Keine Angaben zu UEs |
Department of Psychology in the Graduate School of The University of Alabama |
Risk of Bias
SB1: low SB2 unclear PB: high DB: high AB: high RB: unclear
Keine Fallzahlplanung
|
|
||||||||
|
Do Carmo et al., 2017: The feasibility and benefit of a brief psychosocial intervention in addition to early palliative care in patients with advanced cancer to reduce depressive symptoms: a pilot randomized controlled clinical trial. |
RCT prospektiv, monozentrisch, geschlossen, 3 Arme
Eingeschlossen: N=63 Follow-Up1: N=56 Follow-Up2: N=46 Follow-Up3: N=30 Follow-Up4: N=7
ITT-Ansatz (kA zu Imputation); ausgewertet: N=37-58 (je nach Zeitpunkt und Outcome)
Land: Brasilien August 2014 – August 2015 |
Krebs im Endstadium
4 x Lungenkrebs 12 x Brustkrebs, 5 x Kolon/Rektal 1x Prostatakrebs 4x Magenkrebs 3x Kopf&Nackenkrebs
6x Gebärmutterkrebs
6 x andere Krebsarten
Geschlecht: 68.4 % weiblich (Arm A), 63.6 % weiblich (Arm B)
Alter: 18-75 Mittelwert: -
|
Arm A: NR=17 NFU1=16 NFU2=12 NFU3=7 NFU4=0 5x Sessions Kurze psychosoziale Intervention & systematische Palliativversorgung, über 5 Wochen
Arm B: NR=22 NFU1=21 NFU2=18 NFU3=12 NFU4=3 systematische Palliativversorgung
Arm C: NR=22 NFU1=19 NFU2=16 NFU3=11 NFU4=4 CAU
|
Erhebungszeitpunkt Baseline Follow-Up1 = Post-Intervention (ca. 6 Wochen) Follow-Up2 (ca. 17,5 Wochen) Follow-Up3 (ca. 25 Wochen) Follow-Up4 (ca. 40 Wochen)
Primäre Endpunkte: 1. Depressivität (HADS-D, PHQ-9)
Sekundäre Endpunkte: 2. QoL (EORTC-QLQ-C15-Pal) Angst (HADS-A) |
Während der Intervention: 1. Depressivität à keine sign. Gruppe x Zeit-Interaktion à sign. Zeiteffekt (Verbesserung in allen Gruppen über die Zeit)
2. QoL à keine sign. Gruppe x Zeit-Interaktion à sign. Zeiteffekt (Verbesserung in allen Gruppen über die Zeit)
3. Angst à keine sign. Gruppe x Zeit-Interaktion à sign. Zeiteffekt (Verbesserung in allen Gruppen über die Zeit)
|
Keine Angaben zu UEs |
This study received financial support from the São Paulo Research Foundation (FAPESP; grant no. 2014/22052–5) Laut Angaben kein COI |
Risk of Bias
SB1: low SB2 unclear PB: high DB: high AB: low RB: low
Die Autoren geben an, dass die verwendete ITT-Analyse den Kontaminationsbias wahrscheinlich reduziert hat.
Hohe Attritionsrate wegen Tod
Pilotstudie
Geplante Fallzahl (N=150) nicht erreicht
|
|
||||||||
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