Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06094218

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Harding Hospital

Columbus, Ohio, United States, 43210

Actively Recruiting

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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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