NCT07388641

Brief Summary

The VA has been focused on reducing the number of homeless Veterans nationally. However, it has been very difficult to increase the level of productive activities--including work, school, and training--for homeless-experienced Veterans (HEVs), even when the VA provides substantial case management and support services in addition to housing. The overarching aim of this proposed treatment project is to validate an innovative psychosocial intervention (a combination of Motivational Interviewing and Cognitive Behavioral Therapy; MI-CBT) that is designed to enhance motivation and increase productive community integration in Veterans who have experienced homelessness. The efficacy of this new intervention will be evaluated in a randomized control trial that includes 24 weeks of active treatment, and a follow up assessment, compared with a control condition. The results of the proposed study will have clinical and functional impact for Veterans by helping HEVs to achieve fuller community integration.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
106

participants targeted

Target at P50-P75 for not_applicable

Timeline
61mo left

Started Aug 2026

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 28, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

February 5, 2026

Completed
6 months until next milestone

Study Start

First participant enrolled

August 3, 2026

Expected
4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 3, 2030

1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

August 3, 2031

Last Updated

February 10, 2026

Status Verified

February 1, 2026

Enrollment Period

4 years

First QC Date

January 28, 2026

Last Update Submit

February 5, 2026

Conditions

Keywords

motivationmotivational interviewingpsychosocial interventionworkcommunity integration

Outcome Measures

Primary Outcomes (2)

  • Action subscale of the University of Rhode Island Change Assessment Scale

    Measure of attitudes and activities related to motivation for productive activities. The range is 8-40 in which higher scores indicate more willingness to change.

    baseline, midpoint at 12 weeks, post-treatment at 24 weeks, and follow-up at 36 weeks

  • Service Use and Resource Form (SURF)

    average number of hours of productive activities per week for past month

    baseline, midpoint at 12 weeks, post-treatment at 24 weeks, and follow-up at 36 weeks

Secondary Outcomes (1)

  • Measure of willingness to exert effort on a cognitive task (Deck choice task)

    baseline, midpoint at 12 weeks, post-treatment at 24 weeks, and follow-up at 36 weeks

Study Arms (2)

MI-CBT

EXPERIMENTAL

Combination of Motivational Interviewing and Cognitive Behavioral Therapy

Other: Motivational Interviewing and Cognitive Behavioral Therapy

Health Lifestyles

ACTIVE COMPARATOR

An educational program that instructs participants on important concepts in nutrition, exercise, and stress management.

Other: Healthy Behavior Training

Interventions

Psychosocial intervention to increase motivation for work and productive activities

Also known as: MI-CBT
MI-CBT

An educational program on nutrition, exercise, and stress management.

Also known as: Healthy Lifestyles
Health Lifestyles

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Veteran
  • fluent in English
  • history of homelessness and currently housed through VA HUD-VASH housing programs
  • expressed willingness to work on a school, work, or training goals

You may not qualify if:

  • no clinically significant medical, neurological, or physical condition that would interfere with providing informed consent or valid assessments
  • no visible sign of intoxication on the laboratory assessment visits

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

VA Greater Los Angeles Healthcare System, West Los Angeles, CA

West Los Angeles, California, 90073-1003, United States

Location

MeSH Terms

Interventions

Motivational InterviewingCognitive Behavioral Therapy

Intervention Hierarchy (Ancestors)

Directive CounselingCounselingMental Health ServicesBehavioral Disciplines and ActivitiesHealth ServicesHealth Care Facilities Workforce and ServicesBehavior TherapyPsychotherapy

Study Officials

  • Michael F Green, PhD

    VA Greater Los Angeles Healthcare System, West Los Angeles, CA

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Peter C Hunt, PhD MPH BA

CONTACT

John J Fraser, DPT PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
The assessments will be done by staff members who are entirely unaware of the treatment condition.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Random assignment to experimental psychosocial treatment of active control.
Sponsor Type
FED
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 28, 2026

First Posted

February 5, 2026

Study Start (Estimated)

August 3, 2026

Primary Completion (Estimated)

August 3, 2030

Study Completion (Estimated)

August 3, 2031

Last Updated

February 10, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Locations