Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07283757

PTSD Treatment for Incarcerated Men and Women: AV

Led by University of Wisconsin, Madison · Updated on 2026-01-30

900

Participants Needed

1

Research Sites

205 weeks

Total Duration

On this page

Sponsors

U

University of Wisconsin, Madison

Lead Sponsor

A

Arnold Ventures

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research will help identify if a PTSD treatment group, called Cognitive Processing Therapy (CPT), that is used in community settings is helpful in reducing PTSD symptoms among people who are incarcerated. The goal of CPT is to create a space for people to modify unhelpful beliefs related to trauma. A total of 692 participants will be enrolled from 6 locations and can expects to be on study for up to 24 weeks.

CONDITIONS

Official Title

PTSD Treatment for Incarcerated Men and Women: AV

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Enrolled from the Department of Corrections trauma treatment waitlist
  • No active symptoms of psychosis that interfere with group participation
  • No active suicidal ideation with intent or plan
  • Able and willing to participate in group therapy
  • 18 years old or older
  • Meet PCL-5 criteria for current PTSD diagnosis within 2 months of enrollment
  • No scheduled release date before the end of the treatment group
  • Able to understand the consent form as measured by the consent quiz
  • Have not participated in previous CPT groups with the University of Washington project
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Psychiatric Institute and Clinic

Madison, Wisconsin, United States, 53719

Actively Recruiting

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Research Team

M

Michael R Koenigs, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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