Using VA Peer Specialists to Help Prevent Veteran Suicide
Official title: Testing the Use of VA Peer Specialists to Prevent Veteran Suicide
Run by VA Office of Research and Development · NCT07286383 · Data updated 2026-11-12
This study tests whether 12 one-on-one sessions with a VA Peer Specialist over 3 months can help reduce suicide risk among Veterans with serious mental illness.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 306 (estimated) |
| Sponsor | VA Office of Research and Development Federal |
| Locations | 3 sites (Baltimore, Maryland and 2 other locations) |
| Status | Recruiting |
| Started | September 1, 2026 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2029 |
| Registry record updated | September 8, 2026 |
| Trial ID | NCT07286383 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Veterans with serious mental illness at moderate to high suicide risk in the prior 3 months and current suicidal ideation (PHQ-9 item 9 > 0) who can provide informed consent.
✕Probably not a fit
Individuals without current suicidal ideation or those unable to participate in a 3-month, 12-session program may not benefit from this approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The trial compares PREVAIL-VA, a 3-month program of semi-structured conversations focusing on hope, belonging, support, and safety, delivered by trained VA Peer Specialists to Veterans at risk for suicide versus usual care. It targets Veterans with serious mental illness and recent suicide risk indicators. The study uses a randomized or controlled design to assess whether peer-led support improved outcomes related to suicidality and recovery. PSs bring lived experience to support recovery-oriented care, aiming to expand access to evidence-based, personalized services within the VA system. This is the first rigorous test of a peer-delivered suicide prevention approach in the VHA.
Why it matters
Potential benefit: If successful, the intervention could increase recovery-oriented support and reduce suicide risk among Veterans by expanding VA access to peer-delivered care.
How similar studies have gone: Previous research shows peer specialists improve various outcomes in Veterans with SMI, but this is the first rigorous trial testing a peer-delivered suicide prevention service in the VA.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: There are two Inclusion criteria: * Moderate to high suicide risk according to one of the following occurring in the prior 3 months: * a completed Comprehensive Suicide Risk Evaluation (CSRE) indicating intermediate or high acute or chronic risk * a high-risk suicide PRF * a suicide attempt indicated on a Suicide Behavior or Overdose Report (SBOR) * a suicide safety plan completed in the past 6 months AND * Current suicidal ideation according to the 9th item of the Patient health questionnaire (PHQ-9) \> 0 at enrollment * While a positive 9th item usually precedes the CSRE, because the CSRE could have been administered in the 3 months prior to enrollment, the purpose of requiring a positive 9th item is to ensure more recent suicidal ideation. * It may be more difficult to show an intervention effect if the investigators enroll participants with no suicidal ideation at baseline. Exclusion Criteria: * Inability to provide informed consent for any reason, including due to acute psychosis or mania, dementia, or active guardianship or durable power of attorney * These criteria will be determined according to medical record review and, if clarification needed, consultation with a treating provider. * The investigators will also screen for decision-making capacity using the Blessed Orientation, Memory, Concentration (BOMC) Test and a brief quiz about the study. * This quiz will involve an iterative process of querying the participants' understanding of consent information with a 10-item true/false test and providing feedback until an acceptable level of understanding is achieved (must get 100% correct after 3 tries to enroll). * Current or planned receipt of residential or intensive outpatient treatment * Plan to transfer or terminate care in the next 3 months * Homicidal ideation in the past 6 months or violent behavior in the past 12 months
Where it's running
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Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD
Baltimore, Maryland, United States Recruiting -
VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
Pittsburgh, Pennsylvania, United States Recruiting -
VA Ann Arbor Healthcare System, Ann Arbor, MI
Ann Arbor, Michigan, United States Active not recruiting
Study contacts
- Principal investigator: Matthew J Chinman, PhD — VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
- Study coordinator: Matthew J Chinman, PhD
- Email: matthew.chinman@va.gov
- Phone: (412) 360-2438
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.