What this study is
The purpose of this study is to test the feasibility and acceptability of an evidence-based treatment for depression delivered over an ipad, computer, or smartphone can help Adult Protective Services (APS) clients with their activities of daily living to evaluate whether reductions on measures of depression and apathy (a) mediate reduced Elder Neglect/Self Neglect (EN/SN) behaviors; and (b) whether secondary posited mediating mechanisms are also active in impacting depression and apathy
What's being tested
- APS Treatment as Usual
Intervention · BEHAVIORAL
APS agencies conduct in-home investigations of alleged abuse and neglect against disabled and older adults. Investigations result in short-term stop-gap measures, primarily brief case-management centering on referral linkage to community-based services and provision of resource allocation. No direct psychological services or treatments are provided by APS, however referral to other services is also standard.
- Intervention-Behavioral Activation (BA)
Intervention · BEHAVIORAL
Participants will be will be guided through 8 one-hour sessions via home telehealth by the study community health worker. Each weekly < 60 minute BA session will include modules focusing on 1) Psychoeducation for depression and techniques for self-management, including pharmacologic and psychosocial treatment options; 2) Introduction of BA and guided problem-solving techniques to enhance self efficacy for managing depression and other chronic illnesses; 3) BA and problem-solving techniques to support medication management and adherence strategies; 4) BA to develop strategies and techniques for communicating with health providers and/or support resources to foster positive mood and self management; and 5) Developing a relapse prevention plan, which includes identifying triggers for lower functioning, support resources, and practice of BA techniques.
Study details
- Sponsor
- The University of Texas Health Science Center, Houston
- Conditions
- Depression in Old Age
- Enrolling
- 50 people
- Starts
- 2025-07-21
- Est. completion
- 2026-03-31
- Design
- Open-label, randomized, parallel groups
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 65 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- APS Case in APS Region VI- Must have open case
- PHQ 9 score- Must have score of nine (9) or more
You can't join if
- Previous mental health diagnosis of bipolar disorder, psychotic disorders, and moderate to severe dementia
- Assessment of Consent Proxy- Those who need assessment of consent proxy
- Suicidal Intent (as indexed by PhQ-9 question 9)- Those scoring 2 or 3
- Current Alcohol and Drug Dependency- As evidenced by Cut down, Annoyed, Guilty, and Eye-opener (CAGE) score of 3 or more
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openThe University of Texas Health Science Center at Houston
Houston, Texas, United States
- Leila Wood, PhD, MSSW · Contact(713) 486-2700Leila.G.Wood@uth.tmc.edu
- Jason Burnett · Contact(713) 873-4685Jason.Burnett@uth.tmc.edu
Study team
Sponsor
The University of Texas Health Science Center, Houston
Study ID HSC-MS-24-1021
Principal investigator
Leila Wood, PhD, MSSW
The University of Texas Health Science Center, Houston
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.