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Behavioral Intervention

Cognitive Behavioral Therapy for PTSD

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
* Must be enrolled in our on-going parallel study - "Cognitive Behaviour Therapy with Mindfulness Course for Building Workplace Resilience: A Pilot Randomized Controlled Trial"
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 month
Awards & highlights
No Placebo-Only Group

Summary

This trial will examine whether a 5-session class focused on teaching introductory CBT skills can help prevent PTSD and related conditions in public safety personnel.

Who is the study for?
This trial is for public safety personnel who are part of an ongoing study on using Cognitive Behavioral Therapy with Mindfulness (CBTm) to build workplace resilience. It's designed to help prevent PTSD and manage stress.
What is being tested?
The trial tests if a 5-session CBTm class can increase brain connectivity associated with resilience against PTSD in public safety workers, by comparing fMRI scans before and after the course.
What are the potential side effects?
Since this intervention involves therapy classes rather than medication, typical medical side effects are not expected. Participants may experience emotional discomfort discussing traumatic events.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 month
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 month for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Connor-Davidson Resilience Scale
PTSD resilience-related brain connectivity pattern scores
Posttraumatic Checklist-5

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: ActiveExperimental Treatment1 Intervention
5-week CBTm
Group II: WaitlistedActive Control1 Intervention
Waitlisted (will receive 5-week CBTm 3 months after).

Find a Location

Who is running the clinical trial?

University of ManitobaLead Sponsor
621 Previous Clinical Trials
206,523 Total Patients Enrolled
University of ReginaOTHER
55 Previous Clinical Trials
8,900 Total Patients Enrolled
~6 spots leftby Dec 2025
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