Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04335487

Internet-Delivered Cognitive Behaviour Therapy for PTSD Among Public Safety Personnel

Led by University of Regina · Updated on 2026-04-29

300

Participants Needed

1

Research Sites

403 weeks

Total Duration

On this page

Sponsors

U

University of Regina

Lead Sponsor

G

Government of Canada

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study evaluates two Internet-delivered cognitive behavioural therapy (ICBT) interventions: one for symptoms of posttraumatic stress disorder (PTSD) and one for symptoms of anxiety, depression, and PTSD. Both interventions have been tailored for Canadian public safety personnel (PSP). Outcomes of interest include preference for disorder-specific or transdiagnostic care, engagement with the interventions, changes in symptoms and functioning, and strengths and limitations of implementing ICBT with Canadian PSP.

CONDITIONS

Official Title

Internet-Delivered Cognitive Behaviour Therapy for PTSD Among Public Safety Personnel

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older
  • Residing in Saskatchewan for the duration of the intervention
  • Endorsing symptoms of post-traumatic stress
  • Able to access a computer and internet service
  • Willing to provide a physician as emergency contact
Not Eligible

You will not qualify if you...

  • High suicide risk
  • Suicide attempt or hospitalization in the last year
  • Primary problems with psychosis, alcohol or drug problems, or mania
  • Currently receiving regular psychological treatment
  • Concerns about Internet-delivered cognitive behavioural therapy (ICBT)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Psychology and Collaborative Centre for Justice and Safety

Regina, Saskatchewan, Canada, S4S 0A2

Actively Recruiting

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Research Team

H

Heather D Hadjistavropoulos, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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