CClinicalTrials.gg
RecruitingNCT07388641MI-CBTUpdated Sep 30, 2026

Improving Productive Community Integration in Homeless-experienced Veterans

An interventional study of Motivational Interviewing and Cognitive Behavioral Therapy and Healthy Behavior Training in Homeless Persons, sponsored by VA Office of Research and Development. Recruiting at 1 site in United States. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-30.

Sponsored by VA Office of Research and Development · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
106
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study 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.

Read the detailed description

Significance to the VA: The VA has been heavily 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 project is to validate a recovery-oriented psychosocial intervention that is designed to reduce motivational impairments and increase productive community integration in Veterans who have experienced homelessness and are now housed.

Innovation and Impact: The work in two randomized controlled trials (RCT) has shown that an innovative psychosocial intervention, Motivational Interviewing combined with Cognitive Behavioral Therapy (MI-CBT), significantly increases motivation to achieve personally-relevant functional goals compared with a control procedure. However, the investigators do not know whether this new psychosocial intervention can specifically improve productive aspects of community integration which tend to be most resistant to change. Further, the investigators do not understand the mechanisms through which treatments achieve their benefits. The results of the proposed study will have substantial clinical and functional impact for Veterans by helping HEVs to achieve fuller community integration. The findings will also have the potential to influence the types of psychosocial interventions that are being used in Homeless Programs throughout the VA.

Specific Aims: The proposed project has two aims. Aim 1 is to examine the effects of MI-CBT versus a Healthy Lifestyles control intervention on two primary measures (a proximal outcome of motivation and more distal outcome of behavior) related to productive community integration in HEVs over the 24 weeks of active treatment (i.e., 12 weeks of weekly treatment and 12 weeks of monthly boosters). Aim 2 is to examine the treatment effects of MI-CBT versus the control intervention on a secondary outcome measure of effort allocation. The project has Exploratory Aims to assess whether effort allocation is a mediator of observed changes in motivation and productive behavior and to evaluate whether baseline length of housing is a moderator of the treatment effects.

Methodology: The aims will be evaluated in an RCT that includes 24 weeks of active treatment (group sessions weekly for the first half and boosters every 4 weeks thereafter). A follow up assessment will be conducted at 36 weeks to assess durability. The study will include a total of 106 HEVs who are not involved in jobs, school, or training at their baseline assessment. Participants will be randomly assigned 1:1 to MI-CBT or to an active control condition. There will be two primary outcome measures: the proximal treatment target will be motivation for productive activities; the distal target will be community integration based on average hours of productive activity per week. A secondary outcome will be a measure of effort allocation based on performance on an effort-based decision-making task.

Path to Translation / Implementation: In the proposed RCT, HEVs will be randomly assigned to an innovative psychosocial intervention to improve their productive community activities. It is an efficacy study and is considered a T2-A: Phase II trial which is intended to determine the efficacy of therapy in patients. If the proposed project is successful, the subsequent study would be a larger, multi-site RCT in a broader sample of HEVs. That would move the aims into T2-B: Phase III larger clinical trials to establish efficacy and optimal use in humans.

02

Conditions studied

  • Homeless Persons

Keywords

  • motivation
  • motivational interviewing
  • psychosocial intervention
  • work
  • community integration
03

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • 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
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
106 participants (estimated)

Study arms

  • Experimental
    MI-CBT

    Combination of Motivational Interviewing and Cognitive Behavioral Therapy

    Other: Motivational Interviewing and Cognitive Behavioral Therapy

  • Active comparator
    Health Lifestyles

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

    Other: Healthy Behavior Training

Interventions

  • OtherMotivational Interviewing and Cognitive Behavioral Therapy

    Psychosocial intervention to increase motivation for work and productive activities

    Also known as: MI-CBT

  • OtherHealthy Behavior Training

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

    Also known as: Healthy Lifestyles

05

What researchers measure

Primary outcomes

  1. 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.

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

  2. Service Use and Resource Form (SURF)

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

    Time frame: 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)

    Measure of effort allocation on a cognitive choice task. The range is 0-18 with higher scores indicated more accuracy and effort allocation.

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

06

Study locations

1 of 1 sites recruiting
  • VA Greater Los Angeles Healthcare System, West Los Angeles, CA
    West Los Angeles, California 90073-1003, United States
    • Irma Gvilia, PhD MS · Contact · Irma.Gvilia@va.gov · (818) 891-7711
    • Linda D Nguyen, BS · Contact · linda.nguyen@va.gov · (310) 478-3711
    • Michael F Green, PhD · Principal investigator
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07388641
Lead sponsor
VA Office of Research and Development
Responsible party
Sponsor
First posted
Feb 5, 2026
Start date
Sep 14, 2026
Primary completion
Sep 14, 2030 (estimated)
Completion
Sep 14, 2031 (estimated)
Last update
Sep 30, 2026

Study contacts

Peter C Hunt, PhD MPH BA
Contact
Peter.Hunt3@va.gov
(562) 826-8000 ext. 6113
John J Fraser, DPT PhD
Contact
john.fraser@va.gov
Michael F Green, PhD
principal investigator · VA Greater Los Angeles Healthcare System, West Los Angeles, CA

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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