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Clinical Trials/NCT06910267
NCT06910267RecruitingNot Applicable

Leveraging Adult Protective Service Interaction to Offer Evidence-Based Treatment for Depression in Elder Neglect/Self Neglect

The University of Texas Health Science Center, Houston1 site in 1 country50 target enrollmentStarted: May 15, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
50
Locations
1
Primary Endpoint
Change in depression as assessed by the Patient Depression Questionnaire (PHQ-9)

Study Overview

Brief Summary

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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •APS Case in APS Region VI- Must have open case
  • •PHQ 9 score- Must have score of nine (9) or more

Exclusion Criteria

  • •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

Arms & Interventions

APS Treatment as Usual

Active Comparator

Intervention: APS Treatment as Usual (Behavioral)

Intervention-Behavioral Activation (BA)

Experimental

Intervention: Intervention-Behavioral Activation (BA) (Behavioral)

Outcomes

Primary Outcomes

Change in depression as assessed by the Patient Depression Questionnaire (PHQ-9)

Time Frame: baseline, post-treatment ( 8 weeks after baseline), and 3 months

This is 9 item questionnaire and each is scored from 0 (not at all) to 3 (nearly every day), for a maximum score of 27, higher score indicating more depression

Change in apathy as assessed by the Apathy Motivations Index (AMI)

Time Frame: baseline, post-treatment ( 8 weeks after baseline), and 3 months

This is an 18 item questionnaire and each item is scored on a scale from 0(completely true) to 4(completely untrue), for a maximum score of 72, with higher scores indicating greater apathy

Change in Elder Neglect/Self Neglect (EN/SN) as evidenced by study developed goal attainment scale

Time Frame: baseline, post-treatment ( 8 weeks after baseline), and 3 months

Participants will be given a list of 19 common daily activities and will be asked to pick one or more activities form the list that they would like to start doing or do more regularly each day or week.Each activity will be then scored based on the following scoring criteria, higher score indicating better outcome : (Much less than expected)-2 (Somewhat less than expected)-1 (Expected client outcome)0 (Somewhat better than expected)+1 (Much better than expected)+2

Secondary Outcomes

  • Change in social connection as assessed by the Lubben Social Network Scale(baseline, post-treatment ( 8 weeks after baseline), and 3 months)
  • Change in social isolation as assessed by Patient-Reported Outcomes Measurement Information System (PROMIS 8)(baseline, post-treatment ( 8 weeks after baseline), and 3 months)

Investigators

Sponsor
The University of Texas Health Science Center, Houston
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Leila Wood

professor

The University of Texas Health Science Center, Houston

Study Sites (1)

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