Depressive Symptoms Clinical Trial
Official title:
Feasibility, Acceptance and Efficacy of Metacognitive Training-Silver BeWell in Older Adults
The present study seeks to examine the feasibility, acceptance and efficacy of Metacognitive Training-Silver (MCT-Silver) BeWell among older adults (ages 60 years and older) delivered in a community setting (e.g., social-psychiatric community center, nursing homes, etc.).
Status | Recruiting |
Enrollment | 40 |
Est. completion date | December 2025 |
Est. primary completion date | August 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 60 Years and older |
Eligibility | Inclusion Criteria: - Informed consent - Age 60 years or older - Sufficient command of the German language - Willingness to participate in intervention over a period of 10 weeks (participants who do not attend the intervention, but complete questionnaires will also be included in the analysis) - Visual and auditory acuity adequate for participation in group sessions - Ability to participate in the group setting (ability to participate in the group setting will be assessed during a screening interview (e.g., adequate social skills)). Exclusion Criteria: - Acute suicidality as assessed by BDI-II Item 9 - Dementia (MMSE < 24) or evidence of severe organic brain dysfunction |
Country | Name | City | State |
---|---|---|---|
Germany | University Medical Center Hamburg-Eppendorf | Hamburg |
Lead Sponsor | Collaborator |
---|---|
Universitätsklinikum Hamburg-Eppendorf |
Germany,
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* Note: There are 11 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of sessions attended | The total number of sessions attended (of 10) will be used to assess the feasibility of the intervention | 10 weeks (pre (t0)- to post (t1)) | |
Secondary | Participants' appraisal of the training | Participant's acceptance of the training as measured by a self-developed questionnaire; single items assessing patients' acceptance of the training (1 = low acceptance; 5 = high acceptance); high scores indicate better appraisal of the intervention | after each session weeks 1 through 10; post (10 weeks; t1) and follow-up (3 months; t2) | |
Secondary | Negative effects questionnaire (NEQ) | Negative effects of the intervention will be assessed by the Negative Effects Questionnaire "negative effects of treatment" score (minimum = 0; maximum = 128); higher scores indicate more negative side effects | post (10 weeks; t1) and follow-up (3 months; t2) | |
Secondary | Depression (Beck Depression Inventory - II) | Change in self-assessed depression as measured by the Beck Depression Inventory-II (BDI-II) from baseline to post-assessment (t0 to t1) and follow-up (t0 to t2); 21 items are assessed on a 4-point Likert scale; higher scores indicate more depressive symptoms; (minimum score = 0; maximum score = 63) | baseline (t0), post (10 weeks; t1), and follow-up (3 months; t2) | |
Secondary | Dysfunctional beliefs (18-item Dysfunctional Attitudes Scale) | Change in dysfunctional beliefs as measured by the 18-item Dysfunctional Attitude Scale (DAS-18B) from baseline to post-assessment (t0 to t1) and follow-up (t0 to t2); 18 items are assessed on a 7-point Likert scale; high score indicates more dysfunctional beliefs (minimum = 18; maximum = 126) | baseline (t0), post (10 weeks; t1), and follow-up (3 months; t2) | |
Secondary | Mental Well-Being (Warwick-Edinburgh Mental Well-being Scale) | Change in mental well-being as measured by the short version of the Warwick-Edinburgh Mental Well-being Scale (WEMWBS) from baseline to post-assessment (t0 to t1) and follow-up (t0 to t2); 14 items assessed on a 5-point Likert scale (minimum = 14; maximum = 70). Higher scores indicate better well-being. | baseline (t0), post (10 weeks; t1), and follow-up (3 months; t2) | |
Secondary | Resilience (Resilience Scale) | Change in resilience as measured by the 13-item Resilience Scale from baseline to post-assessment (t0 to t1) and follow-up (t0 to t2); 13 items assessed on a 7-point Likert scale (minimum = 13; maximum = 91). Higher scores indicate more resilience. | baseline (t0), post (10 weeks; t1), and follow-up (3 months; t2) | |
Secondary | Rumination (Ruminative Responses Scale) | Change in rumination measured by the Ruminative Response Scale (RRS) from baseline to post-assessment (t0 to t1) and follow-up (t0 to t2); 10 items assessed on a 4-point Likert scale (minimum = 10; maximum = 40). Higher scores indicate more ruminative behaviors. | baseline (t0), post (10 weeks; t1), and follow-up (3 months; t2) | |
Secondary | Loneliness (UCLA Loneliness scale) | Change in loneliness as measured by the 3-item UCLA Loneliness scale from baseline to post-assessment (t0 to t1) and follow-up (t0 to t2); 3-items assessed on a 4-point Likert scale (minimum = 4; maximum = 12). Higher scores indicate more loneliness. | baseline (t0), post (10 weeks; t1), and follow-up (3 months; t2) | |
Secondary | Self-rated health (EQ5D5L Visual Analog Scale ) | Change in self-rated health as measured by the EQ5D5L Visual Analog Scale from baseline to post-assessment (t0 to t1) and follow-up (t0 to t2); Rating Scale 0 (worst health possible) - 100 (best health possible). | baseline (t0), post (10 weeks; t1), and follow-up (3 months; t2) | |
Secondary | Session-specific effects | Before and after each session during weeks 1 through 10, participants will complete a 40-item questionnaire regarding changes in depressive symptoms, negative (meta)cognitive beliefs and attitudes associated with depression, which are targeted in the MCT-Silver BeWell. Items are assessed on a 6-point LIkert scale (minimum = 40; maximum = 240); high scores indicate more negative beliefs / attitudes | Before and after each session weeks 1 through 10 |
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