Testing the Use of VA Peer Specialists to Prevent Veteran Suicide
Part of paid clinical trials in Baltimore, Maryland.
- Sponsor
- VA Office of Research and Development
- Study ID
- NCT07286383
- Phase
- PHASE3
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Suicide Risk
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- PREVAIL — BEHAVIORAL12 session, peer specialist delivered, suicide prevention program
Study Details
This study examines a novel way to prevent suicide among Veterans with serious mental illness (SMI). It will assess the efficacy of PREVAIL-VA, a 3-month intervention of 12, one-on-one sessions between a Peer Specialist (PS) and a Veteran that involve semi-structured conversations focused on hope, belongingness, support, and safety. PSs are Veterans with SMI trained to use their own experience and recovery to help other Veterans with SMI. PSs have improved mental health outcomes in other research, but this study would be the first to test their efficacy for suicide prevention in VHA. The project will compare outcomes of Veterans at risk for suicide receiving usual care, to PREVAIL-VA. This work is responsive to national calls for Veterans with SMI to receive support that is evidence-based, improves recovery (not just symptoms), and is tailored to individual needs. If successful, PREVAIL-VA could be adopted by the 1400 Peer Specialists employed in VA, greatly increasing the delivery of evidence-based services to Veterans at risk for suicide.
Key Dates
- Start date
- Jul 1, 2026
- Status verified
- Apr 2026
- Primary completion
- Dec 31, 2028
- Completion
- Dec 31, 2029
Study Design
- Enrollment
- 306 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- HEALTH_SERVICES_RESEARCH
Arms
- Experimental: PREVAIL12 session, peer specialist delivered, suicide prevention program
- No Intervention: Usual CareVeterans assigned to this group will receive additional monitoring but no active intervention.
Primary Outcome Measure
Computerized Adaptive Test- Suicide Scale; Columbia-Suicide Severity Rating Scale [ Time Frame: Baseline, 3 months, 6 months ]
Central Contacts
- Matthew J Chinman, PhD(412) 360-2438
- Jessica R Dodge, PhD MSW MPH(734) 845-3609
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD | Baltimore | Maryland | 21201 | |
| VA Ann Arbor Healthcare System, Ann Arbor, MI | Ann Arbor | Michigan | 48105-2303 | - |
| VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA | Pittsburgh | Pennsylvania | 15240 | - |
Find similar trials in Baltimore, MD
Related Studies
- Long-term Observation of Participants With Mood DisordersRecruiting · National Institute of Mental Health (NIMH) · Bethesda, Maryland
- Get Better Together: Relationship Education For Military CouplesRecruiting · Henry M. Jackson Foundation for the Advancement of Military Medicine · Bethesda, Maryland
- Improving Mental Health Treatment for Individuals in Crisis Interacting With the Criminal-Legal SystemRecruiting · Cambridge Health Alliance · Cambridge, Massachusetts
- Orexin Antagonism for Suicide Risk: A Proof-of-Concept Clinical TrialPHASE2 · Recruiting · Marianne Goodman · The Bronx, New York