Improving Productive Community Integration in Homeless-experienced Veterans
MI-CBT
An Innovative Combined Psychosocial Intervention to Improve Productive Community Integration in Homeless-experienced Veterans
2 other identifiers
interventional
106
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2026
Longer than P75 for not_applicable
1 active site
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
CompletedFirst Posted
Study publicly available on registry
February 5, 2026
CompletedStudy Start
First participant enrolled
August 3, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
August 3, 2030
Study Completion
Last participant's last visit for all outcomes
August 3, 2031
February 10, 2026
February 1, 2026
4 years
January 28, 2026
February 5, 2026
Conditions
Keywords
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
EXPERIMENTALCombination of Motivational Interviewing and Cognitive Behavioral Therapy
Health Lifestyles
ACTIVE COMPARATORAn educational program that instructs participants on important concepts in nutrition, exercise, and stress management.
Interventions
Psychosocial intervention to increase motivation for work and productive activities
An educational program on nutrition, exercise, and stress management.
Eligibility Criteria
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
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Michael F Green, PhD
VA Greater Los Angeles Healthcare System, West Los Angeles, CA
Central Study Contacts
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
- 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