Partnered implementation of the veteran sponsorship initiative: protocol for a randomized hybrid type 2 effectiveness-implementation trial.
Joseph C Geraci, Erin P Finley, Emily R Edwards...
https://pubmed.ncbi.nlm.nih.gov/35804354Actively Recruiting
Led by VA Office of Research and Development · Updated on 2026-01-14
630
Participants Needed
2
Research Sites
N/A
Total Duration
V
VA Office of Research and Development
Lead Sponsor
C
Central Texas Veterans Health Care System
Collaborating Sponsor
The trial focuses on the urgent issue of rising suicide rates among the youngest U.S. Veterans aged 18 to 34, particularly during their first year after leaving military service. Researchers are studying the Veteran Sponsorship Initiative, a community-based program designed to reduce reintegration difficulties, psychological distress, and suicidal thoughts by providing personalized support to transitioning servicemembers and Veterans (TSMVs). The study aims to evaluate the initiative's effectiveness and how best to implement it in six Texas cities, with plans for future nationwide expansion. Participants are divided into two groups: one receiving the Veteran Sponsorship Initiative, where each TSMV is paired with a certified volunteer sponsor starting about six months before discharge and continuing for six months after discharge, and a control group following usual transition processes. Sponsors assist TSMVs through regular contact and monthly meetings, helping set goals, develop reintegration plans, and encourage attendance at healthcare appointments. The initiative is supported by community integration coordinators who manage sponsors and facilitate local partnerships. Participants will be assessed at multiple points from baseline through 12 months post-discharge using surveys and interviews to measure reintegration difficulties, psychological health, connectedness, suicidal thoughts and behaviors, and healthcare use. Data will be collected from TSMVs and stakeholders to evaluate barriers and facilitators of the program. The study uses mixed methods, combining quantitative models with qualitative analysis, to guide future implementation and address the critical "deadly gap" period after military discharge.
CONDITIONS
National Sponsorship Program for Transitioning Service Members
You may qualify if you...
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person or virtual)
Duration - Approximately 12 months starting about 6 months prior to discharge and continuing for 6 months post-discharge
Participants receive either the Veteran Sponsorship Initiative, which provides one-on-one certified volunteer sponsors to assist with reintegration tasks before and after military discharge, or transition as usual without intervention.
Regular contact with sponsors including monthly video or in-person sessions; study assessments at baseline, 4, 8, and 12 months
Total: 2 locations
1
James J. Peters VA Medical Center, Bronx, NY
The Bronx, New York, United States, 10468-3904
Actively Recruiting
2
Central Texas Veterans Health Care System Waco VA Medical Center, Waco, TX
Waco, Texas, United States, 76711
Actively Recruiting
J
Joseph C Geraci, PhD
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
PREVENTION
Number of Arms
2
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Joseph C Geraci, Erin P Finley, Emily R Edwards...
https://pubmed.ncbi.nlm.nih.gov/35804354