Post-Traumatic Stress Disorder (PTSD) Clinical Trials

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PTSD Treatment for Incarcerated Men and Women: Arnold Ventures (AV)

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Participants will be enrolled from the Department of Corrections trauma treatment waitlist who have been screened for:

• No active symptoms of psychosis that would interfere with the individual's ability to participate in the group

• 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 the previous CPT groups with UW project

Locations
United States
Wisconsin
Psychiatric Institute and Clinic
RECRUITING
Madison
Contact Information
Primary
Michael R Koenigs, PhD
mrkoenigs@wisc.edu
(608) 263-1679
Time Frame
Start Date: 2025-12-22
Estimated Completion Date: 2029-12
Participants
Target number of participants: 900
Treatments
Experimental: Cognitive Processing Therapy (CPT) group
Participant groups of 6-10 people to receive CPT to treat PTSD over 6 weeks or 12 weeks, depending on session frequency.
No_intervention: Waitlist Control
Participant groups will provide data as a control group first, and will then receive CPT to treat PTSD
Related Therapeutic Areas
Sponsors
Leads: University of Wisconsin, Madison
Collaborators: Arnold Ventures

This content was sourced from clinicaltrials.gov

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