Management of Depression and Social Isolation in Older Adults With Dementia With Home-based Telehealth Delivered Behavioral Activation + Caregiver Facilitation.
- Conditions
- Depression
- Interventions
- Behavioral: Behavioral Activation for Depression
- Registration Number
- NCT04915040
- Brief Summary
The purpose of this study is to evaluate the feasibility of using behavioral activation therapy with caregiver support delivered via telemedicine to older adults with depression and probable mild dementia.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 7
Participant Eligibility Criteria:
- able to speak and understand English;
- a diagnosis of mild dementia, as determined by a Clinical Dementia Rating interview Sum of Boxes (CDR-SB) score in the mild range as defined by a score of 4.5 - 9.0;
- and able to provide informed consent.
Caregiver Eligibility Criteria.
- Beck Depression Inventory (BDI) score below clinical cutoff for depression and able to provide informed consent.
Participant exclusion criteria:
- presence of suicidal ideation with clear intent,
- concurrent enrollment in another clinical trial for depression,
- substance use disorder.
Caregiver exclusion criteria:
- Active psychosis or significant dementia at screening;
- presence of suicidal ideation with clear intent.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Behavioral Activation for Depression Behavioral Activation for Depression -
- Primary Outcome Measures
Name Time Method Feasibility of recruitment as assessed by number of participants enrolled in the study Week 0 Feasibility of data collection as assessed by percent of missing data Week 8 Change in Depression as measured by the Geriatric Depression Scale Week 0, Week 4, Week 8 15-item self-report for each construct (yes/no) . Score goes from 1 to 15, a higher number indicates presence of depression.
Feasibility of retention as assessed by number of participants who complete at least 6 sessions Week 8
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Texas Health Science Center at Houston
🇺🇸Houston, Texas, United States