Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07238192

Augmenting Massed Cognitive Processing Therapy (CPT) to Prevent Suicide Risk Among Patients With PTSD

Led by Ohio State University · Updated on 2026-02-24

190

Participants Needed

1

Research Sites

135 weeks

Total Duration

On this page

Sponsors

O

Ohio State University

Lead Sponsor

U

University of Vermont Medical Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this research is to see if Crisis Response Planning (CRP), a brief strategy designed to help people cope effectively with emotional crises, combined with Cognitive Processing Therapy (CPT), a talk treatment for posttraumatic stress disorder (PTSD), will reduce suicidal thoughts and behaviors.

CONDITIONS

Official Title

Augmenting Massed Cognitive Processing Therapy (CPT) to Prevent Suicide Risk Among Patients With PTSD

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be an active duty service member or veteran aged 18 or older eligible for military medical care
  • Be able to read, write, and speak English
  • Meet diagnostic criteria for PTSD or subthreshold PTSD according to the Clinician Administered PTSD Scale for DSM-5 (CAPS-5)
  • Have active suicidal ideation within the past week or report a suicide attempt (actual, aborted, or interrupted) within the past month
  • Regularly use an iPhone or Android smartphone
Not Eligible

You will not qualify if you...

  • Unable to understand and complete consent and baseline screening questionnaires
  • Current suicide or homicide risk requiring crisis intervention
  • Serious mental health symptoms such as mania, psychosis, or alcohol/substance use disorders needing immediate clinical attention
  • Currently receiving evidence-based psychotherapy for PTSD such as Cognitive Processing Therapy, Prolonged Exposure Therapy, or Written Exposure Therapy

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

Carl R. Darnall Army Medical Center

Fort Hood, Texas, United States, 76544-9800

Actively Recruiting

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Research Team

C

C. Rosie Bauder, PhD, MPH

CONTACT

A

Anna Crouser, MSW

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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