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Cognitive Processing Therapy for PTSD
Study Summary
This trial will study the feasibility and psychological response of Cognitive Processing Therapy (CPT) in incarcerated men and women with PTSD. The study will include 2 groups of 10 individuals in both populations (40 total; 20F/20M). It will run for up to 2 years and participants can expect to be participating for up to 22 weeks.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- I am willing and able to join group therapy sessions.I am 18 years old or older.
- Group 1: Cognitive Processing Therapy (CPT) group
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Is enrollment still open for this research project?
"Affirmative. Evidence on clinicaltrials.gov demonstrates that the trial, which was initially posted on June 6th 2022, is actively recruiting volunteers. The clinical study requires 40 participants to be sourced from 1 site."
How many participants are being recruited for this research endeavor?
"Affirmative. The publicly available information on clinicaltrials.gov reveals that recruitment for this study, which was initially advertised on June 6th 2022, is still ongoing. A total of 40 participants need to be sourced from a single medical facility."
What are the core aims of this experiment?
"The primary endpoint of this study, to be assessed within 6 weeks (concluding at the 12th session), is participant satisfaction as measured by CSQ-8 scores. Secondary objectives include gathering information on why participants discontinued their participation, measuring interest in participating and ascertaining patient eligibility for inclusion."
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