Actively Recruiting
Development of a Treatment Prognosis Calculator for the Prevention of Suicide
Led by Ohio State University · Updated on 2026-02-25
1200
Participants Needed
1
Research Sites
200 weeks
Total Duration
On this page
Sponsors
O
Ohio State University
Lead Sponsor
U
United States Department of Defense
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this interventional study is to develop and test a treatment prognosis calculator to identify which service members with suicidal ideation or behavior are likely to respond well to the current standard of care treatment and which should instead receive Brief Cognitive Behavioral Therapy (BCBT) as a first-line treatment. The main aims of the study are: * Aim 1: To develop a novel treatment prognostic calculator to predict response to treatment as usual (TAU) and identify treatment-seeking military personnel who are unlikely to respond adequately to TAU for the reduction of suicidal ideation. * Aim 2: To evaluate the performance of the treatment prognosis calculator in a new sample of treatment-seeking military personnel and determine whether BCBT is more effective than TAU for those patients who are predicted not to respond adequately to TAU. Participants will receive mental health treatment as it is typically administered by their mental healthcare treatment team. Members of their mental healthcare treatment team may receive intensive training in BCBT. After their provider has received this training, they may use this treatment as part of standard of care treatment. The timing of this training will be determined randomly. Participants will complete self-report assessments at the beginning of the study (baseline) as well as 3, 6, 9 and 12 months after their participant begins. These assessments will include questions about feelings, thoughts, moods, impulses, substance use, and behavior.
CONDITIONS
Official Title
Development of a Treatment Prognosis Calculator for the Prevention of Suicide
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female and male active duty service members
- 18 years old or older
- Currently engaged in mental health treatment at one of the study sites
- Suicidal ideation within the last month as indicated by a score above 0 on the Columbia Suicide Severity Rating Scale Screener-Recent or specific questions on the Scale for Suicidal Ideation
- Able to understand and speak English
- Able to provide informed consent
You will not qualify if you...
- Psychiatric or medical conditions that prevent providing informed consent or participating in treatments, such as psychosis, mania, or acute intoxication
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Harding Hospital
Columbus, Ohio, United States, 43210
Actively Recruiting
Research Team
J
Jay Fournier, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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