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Behavioral Intervention

Trauma-exponsed control for Post-Traumatic Stress Disorder

N/A
Waitlist Available
Research Sponsored by University of Manitoba
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 13 weeks
Awards & highlights

Study Summary

This trial will investigate whether cognitive processing therapy can help improve symptoms of PTSD by changing abnormal brain connectivity.

Eligible Conditions
  • Post-Traumatic Stress Disorder

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~13 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 13 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Clinician-Administered PTSD Scale (CAPS) for the DSM-V
Secondary outcome measures
functional connectivity

Trial Design

3Treatment groups
Active Control
Group I: no trauma healthy controlActive Control1 Intervention
Scanned twice (13 weeks apart) without any intervention
Group II: Trauma-exponsed controlActive Control1 Intervention
Will receive Cognitive Processing Therapy
Group III: PTSDActive Control1 Intervention
Will receive Cognitive Processing Therapy

Find a Location

Who is running the clinical trial?

University of ManitobaLead Sponsor
595 Previous Clinical Trials
199,413 Total Patients Enrolled
Workers Compensation Board of ManitobaUNKNOWN
2 Previous Clinical Trials
175 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
CPT-fMRI Study for PTSD
Ji Hyun Ko, PhD 2017. "CPT-fMRI Study for PTSD". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT03229915.
~9 spots leftby Apr 2025
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