Actively Recruiting
Evaluation of a Telehealth Case Management Intervention to Prevent Suicide Among Soldiers Discharged From Psychiatric Hospitalization
Led by Uniformed Services University of the Health Sciences · Updated on 2026-03-25
1500
Participants Needed
1
Research Sites
183 weeks
Total Duration
On this page
Sponsors
U
Uniformed Services University of the Health Sciences
Lead Sponsor
H
Harvard Medical School (HMS and HSDM)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study evaluates the effectiveness of Pathfinding, a 6-month, remotely-delivered case management intervention designed to decrease suicidal behavior among active-duty Regular Army soldiers recently discharged from inpatient psychiatric treatment. Soldiers discharged from military treatment facilities across the U.S. will be identified and recruited to participate. Those who consent will be randomly assigned to receive either Treatment As Usual (TAU), which is the Army's standard post-discharge care, or TAU plus Pathfinding. Participants will complete a baseline assessment and follow-up assessments 6 months and 12 months later. The 6- and 12-month follow-up periods will also include examination of participants' electronic healthcare data and Army administrative data. The overall goals of the study are: (1) to evaluate whether Pathfinding decreases suicidal behaviors among soldiers transitioning from psychiatric hospitalization back to the community; and (2) to determine which discharged soldiers are most likely to benefit from the Pathfinding intervention versus TAU alone.
CONDITIONS
Official Title
Evaluation of a Telehealth Case Management Intervention to Prevent Suicide Among Soldiers Discharged From Psychiatric Hospitalization
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Active duty Regular Army soldiers recently discharged from inpatient psychiatric care at a military treatment facility in the US
- Access to telephone and computer (including smartphone)
You will not qualify if you...
- Impaired ability to provide informed consent
- Terminal illness
- Failure to complete baseline survey within 30 days of discharge
- Positive screen for post-discharge suicide-related behaviors
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Uniformed Services University of the Health Sciences
Bethesda, Maryland, United States, 20814
Actively Recruiting
Research Team
P
Pathfinding Study
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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