Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06285708

Enhancing the Effectiveness of Prolonged Exposure Among Suicidal Individuals With PTSD

Led by Ohio State University · Updated on 2026-04-03

100

Participants Needed

1

Research Sites

113 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The long-term goal of this study is to reduce suicidal thoughts and behaviors among treatment-seeking individuals who also have posttraumatic stress disorder (PTSD). Prolonged exposure (PE) and crisis response plan (CRP) have demonstrated empirical support for reducing suicide attempts as compared to treatment as usual. However, no studies to date have assessed their effectiveness when used in combination. In light of this knowledge gap, the primary objective of this study will be to test the effectiveness of PE augmented with CRP as compared to PE with care as usual (self-guided treatment plan), an active comparator, for the reduction of suicide ideations and attempts for individuals with comorbid PTSD.

CONDITIONS

Official Title

Enhancing the Effectiveness of Prolonged Exposure Among Suicidal Individuals With PTSD

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Current diagnosis of PTSD or subthreshold PTSD
  • Ability to speak and understand the English language
  • Ability to complete the informed consent process
Not Eligible

You will not qualify if you...

  • Substance use disorder requiring medical management
  • Imminent suicide risk warranting inpatient hospitalization or suicide-focused treatment
  • Impaired mental status that precludes the ability to provide informed consent (e.g., intoxication, psychosis, mania)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Ohio State University

Columbus, Ohio, United States, 43210

Actively Recruiting

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Research Team

J

Jaryd Hiser, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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