Fall Clinical Trial
— TBFOfficial title:
Integrated Tele-Behavioral Activation and Fall Prevention for Low-income Homebound Older Adults With Depression
This study will test clinical and cost effectiveness of an integrated tele- and bachelor's-level counselor/coach delivered behavioral activation (BA) and fall prevention (FP) for low-income homebound older adults. The long-term objective of the proposed study is to improve access to depression treatment and fall prevention for growing numbers of low-income homebound seniors. We plan to recruit 320 low-income, racially diverse homebound seniors who are served by a home-delivered meal (HDM) program and other aging-service agencies in Central Texas. In a 4-arm, pragmatic clinical trial with randomization prior to consent, the participants in the integrated Tele-BA and FP (TBF hereafter) arm will receive 5 Tele-BA sessions and 4 in-home FP sessions. Those in the Tele-BA or FP alone arms will receive the respective intervention and 4 bimonthly telephone check-in (booster) calls, and those in the Attention Control (AC) arm will receive 5 weekly telephone check-in calls followed by 4 bimonthly follow-up calls. Follow-up assessments will be at 12, 24, and 36 weeks after baseline.
Status | Recruiting |
Enrollment | 320 |
Est. completion date | December 31, 2026 |
Est. primary completion date | December 31, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 50 Years to 100 Years |
Eligibility | Inclusion Criteria: - Age 50+ - English or Spanish proficiency - 24-item Hamilton Rating Scale for Depression score > 15 - 12-item Fall Risk Questionnaire score >4 Exclusion Criteria: - Recently (< 4 weeks) initiated or modified antidepressant pharmacotherapy - High suicide risk - Probable dementia - Bipolar disorder - Substance use/misuse - Current participation in any psychotherapy or FP program - Bedbound status |
Country | Name | City | State |
---|---|---|---|
United States | University of Texas at Austin | Austin | Texas |
Lead Sponsor | Collaborator |
---|---|
University of Texas at Austin | Baylor College of Medicine |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes from baseline depressive symptom at 12, 24, and 36 weeks | 24-item Hamilton Rating Scale for Depression score (score range: 15-40; decreased score since baseline is a positive outcome) | at 12, 24, and 36 weeks after baseline | |
Primary | Changes from baseline fall count and injury at 12, 24, and 36 weeks | Changes in six monthly falls calendar data (reduced number of falls since baseline is a positive outcome) | monthly (form 12 weeks to 36 weeks) | |
Primary | Changes from baseline EuroQol-5D score at 12, 24, and 36 weeks | Cost-effectiveness measure (score range: 0-20; decreased score since baseline is a positive outcome) | at 12, 24, and 36 weeks after baseline | |
Primary | Changes from baseline physical and mental health service use | Changes in Cornell Services index data (decreased ED visits and hospitalization since baseline is a positive outcome) | at 12, 24, and 36 weeks after baseline | |
Primary | Changes from baseline disability score at 12, 24, and 36 weeks | Changes in 12-item World Health Organization Disability Assessment Schedule score (score range: 0-46; decreased score since baseline is a positive outcome) | at 12, 24, and 36 weeks after baseline | |
Primary | Changes from baseline social engagement and activities score at 12, 24, and 36 weeks | Changes in 10-item Social Engagement and Activities Questionnaire score (score range: 0-50; increased score since baseline is a positive outcome) | at 12, 24, and 36 weeks after baseline | |
Primary | Changes from baseline satisfaction with social roles & activities at 12, 24, and 36 weeks | C (score range: 0-32; increased score since baseline is a positive outcome) | at 12, 24, and 36 weeks after baseline | |
Secondary | Changes from baseline fear of falling at 12, 24, and 36 weeks | Changes in 7-item Falls Efficacy Scale International score (score range: 7-28; decreased score since baseline is a positive outcome) | at 12, 24, and 36 weeks after baseline | |
Secondary | Changes from baseline exercise frequency at 12, 24, and 36 weeks | Changes in RAPA (Rapid Assessment of Physical Activities) (score range: 1-9; increased score since baseline is a positive outcome) | at 12, 24, and 36 weeks after baseline |
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