Peer Support for Whole Health for Veterans
Randomized Controlled Trial of Peer Support for Whole Health
2 other identifiers
interventional
240
1 country
2
Brief Summary
This project is evaluating a new intervention, Peer Support for Whole Health. Peer Support for Whole Health is delivered by peer support specialists, Veterans who are in recovery from mental health or substance use concerns who are employed to help other Veterans. Peer Support for Whole Health uses the Whole Health model to talk about values and self-care in all areas of life. Peer Support for Whole Health is designed to help Veterans who have difficulty with their relationships, work, or day-to-day life and may have behavioral health concerns. Peer Support for Whole Health is designed for Veterans in primary care who are not engaged in mental health or substance use treatment. The goal of this study is to find out whether Peer Support for Whole Health helps Veterans with relationships, work, or day-to-day life. This project will also study whether Peer Support for Whole Health improves well-being and mental health. Finally, this study will seek to understand how Peer Support for Whole Health works and which Veterans it helps the most.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2027
Longer than P75 for not_applicable
2 active sites
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 22, 2026
CompletedFirst Posted
Study publicly available on registry
February 4, 2026
CompletedStudy Start
First participant enrolled
January 4, 2027
ExpectedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2030
Study Completion
Last participant's last visit for all outcomes
July 1, 2030
February 4, 2026
January 1, 2026
3.5 years
January 22, 2026
January 27, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Inventory of Psychosocial Functioning
The Inventory of Psychosocial Functioning measures all key areas of psychosocial functioning including social functioning (e.g., family, parenting, romantic relationships, friendships), vocational functioning (e.g., work and school), and self-care (e.g., chores, diet, medical care).
9 months
Secondary Outcomes (2)
Well-Being Signs
9 months
Depression Anxiety and Stress Scales (DASS-21)
9 months
Study Arms (2)
Peer Support for Whole Health
EXPERIMENTALIn this arm, Veteran participants will receive Peer Support for Whole Health from VA peer support staff.
Self-Directed Whole Health
ACTIVE COMPARATORIn this arm, Veteran participants will receive information about Whole Health tools and resources from research staff.
Interventions
Veteran participants have an appointment with research staff and receive information about VA Whole Health tools and resources including handouts, websites, and apps.
Veteran participants have one-on-one appointments with VA peer support staff to talk about VA Whole Health including goals and progress.
Eligibility Criteria
You may qualify if:
- Veterans
- enrolled in primary care at one of the study sites
- have some challenges with day-to-day life (e.g., relationships, work, school, getting things done) based on a standard questionnaire
- have a recent primary care medical record note documenting potential behavioral health concerns or symptoms
- fully understand the research study
You may not qualify if:
- not be enrolled in current peer support services, mental health services, or other similar services
- at risk for suicide or other high-risk concerns
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Syracuse VA Medical Center, Syracuse, NY
Syracuse, New York, 13210-2716, United States
Michael E. DeBakey VA Medical Center, Houston, TX
Houston, Texas, 77030-4211, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Emily M. Johnson, PhD
Syracuse VA Medical Center, Syracuse, NY
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- FED
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 22, 2026
First Posted
February 4, 2026
Study Start (Estimated)
January 4, 2027
Primary Completion (Estimated)
July 1, 2030
Study Completion (Estimated)
July 1, 2030
Last Updated
February 4, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will share
Anonymous, de-identified data can be made available upon reasonable written request following conclusion of the trial. All identifiable information will be removed prior to sharing, and the minimum amount of data required to achieve the purposes of the request will be shared.