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Improving Adult Protective Services Client Outcomes: A Stepped-Care Social and Mental Health Engagement Program

Improving Adult Protective Services Client Outcomes: A Stepped-Care Social and Mental Health Engagement Program

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06257095
Enrollment
400
Registered
2024-02-13
Start date
2023-08-09
Completion date
2026-10-31
Last updated
2026-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression in Old Age

Keywords

social engagement, Adult Protective Services (APS), elder abuse, self neglect

Brief summary

The purpose of this study is to ascertain the feasibility and effectiveness of an 8-week social engagement program aimed at reducing depression and increasing social engagement among seniors who are transitioning out of Adult Protective Services (APS) for either elder abuse or self-neglect.

Interventions

BEHAVIORALStepped-care social and mental health engagement

Each student will be matched to an older adult and the students will make one call o the older adult which lasts upto 1 hour each week for 8 weeks. Ending each call, the student will assess symptoms of depression anxiety through questionnaires. If the participant responds yes on two consecutive calls to any of these questions, they will be asked if they would like to receive a call from the University of Texas Health Science Center Trauma and Resilience Center to discuss free counseling services.

BEHAVIORALAPS Usual care

Participants will receive a phone call for data collection. Then they will be offered to receive an abbreviated version of the stepped-care social and mental health engagement intervention, lasting only 6-weeks with the option to continue calls if agreeable between the student and older adult.

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER
Department of Health and Human Services
CollaboratorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Older Adults * an APS validated EM/SN case * able to provide informed consent * able to speaks English or Spanish * able to hear sufficiently using the telephone * transitioning out of APS intervention (i.e. in the case closure phase of the APS service). Student * college or university student * enrolled in a health-related program * commit to making 8-weekly consecutive calls * complete the required 1-hour training and assessment.

Exclusion criteria

Older Adults * Individuals needing a proxy to consent * suspected or confirmed decision-making capacity impairments or uncontrolled psychiatric illnesses such as schizophrenia, paranoia, delusion, or delirium Student -only engaging in the program to fulfill some educational requirement

Design outcomes

Primary

MeasureTime frameDescription
Change in social isolation assessed by the Duke Social Support Index (DSSI-6)baseline, 4-week and 8-week follow-upThis is a 6-item questionnaire and each is measured from 1(hardly ever) to 3(most of the time) for a maximum score of 18, higher score indicating greater social support
Change in loneliness as assessed by the University of California Los Angeles (UCLA )loneliness scalebaseline, 4-week and 8-week follow-upThis is a 20-item questionnaire , each item is rated as either O ("I often feel this way"), S ("I sometimes feel this way"), R ("I rarely feel this way"), N ("I never feel this way") for a score range of 0-3,for a maximum score of 60, higher score indicating worse outcome
Change in depression as assessed by the PATIENT HEALTH QUESTIONNAIRE (PHQ-9)baseline, 4-week and 8-week follow-upThis is a 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
Recurrence of Elder mistreatment (EM)From participant's first call to 1 month post final callThis is a yes or no questionnaire that will be answered by adult protective services (APS)
Recurrence of self neglect (SN)From participant's first call to 1 month post final callThis is a yes or no questionnaire that will be answered by adult protective services (APS)

Secondary

MeasureTime frameDescription
Change in anxiety as assessed by the Generalized Anxiety Disorder scale (GAD-7)baseline, 4-week and 8-week follow-upThis is a 7-item questionnaire , each is scored from 0(not at all) to 3(nearly every day), for a score range of 0-21 higher score indicating more anxiety
Change in resilience as assessed by the Brief Resilience Scalebaseline, 4-week and 8-week follow-upThis is a 6-item questionnaire, questions 1, and 5 are scored from 1(strongly disagree) to 5(strongly agree) and questions 2, 4 and 6 are reverse scored , for a score range of 6-30. The total score is then divided by the number of questions answered to get the final score. higher score indicating more resilience.
Change in Anxiety as Assessed by the Generalized Anxiety Disorder 2-Item Scale (GAD-2)baseline, 4-week and 8-week follow-upThis is a 2 item questionnaire and each is scored from 0(not at all) to 3( nearly every day).Total scores range from 0 to 6, with higher scores indicating greater anxiety symptom severity. A score of ≥3 is considered a positive screen for clinically significant anxiety.
Change in Depressive Symptoms as Assessed by the Patient Health Questionnaire-2 (PHQ-2)baseline, 4-week and 8-week follow-upThis is a 2 item questionnaire and each is scored from 0(not at all) to 3(nearly every day) for a total score range of 0-6,higher scores indicate greater depressive symptom severity

Countries

United States

Contacts

CONTACTJason Burnett, PhD
Jason.Burnett@uth.tmc.edu(713) 873-4685
CONTACTJordan Broussard, MS
Jordan.Broussard@uth.tmc.edu713 500 0321
PRINCIPAL_INVESTIGATORJason Burnett, PhD

The University of Texas Health Science Center, Houston

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 4, 2026