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Internet-Delivered Cognitive Behavioural Therapy for PTSD
N/A
Recruiting
Led By Heather D Hadjistavropoulos, PhD
Research Sponsored by University of Regina
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
18 years of age or older
Be older than 18 years old
Must not have
Currently receiving regular psychological treatment
Timeline
Screening 3 weeks
Treatment Varies
Follow Up screening and 1, 2, 3, 4, 5, 6, 7, 8, 12, 16, 26, and 52 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial looks at whether ICBT (a form of therapy delivered via the internet) is effective for treating PTSD, anxiety, and depression in Canadian public safety personnel.
Who is the study for?
This trial is for Canadian public safety personnel in Saskatchewan, aged 18 or older, who are experiencing symptoms of post-traumatic stress. Participants must have internet access and agree to provide a physician contact. It's not suitable for those with recent suicide attempts, hospitalization, substance abuse issues, psychosis or mania, ongoing psychological treatment, or high suicide risk.
What is being tested?
The study tests two online cognitive behavioural therapy courses tailored for PTSD and related mental health issues like anxiety and depression among public safety workers. The goal is to see which course works better for symptom improvement and how participants engage with the online format.
What are the potential side effects?
While ICBT typically has fewer side effects than medication, some may experience discomfort discussing traumatic events or temporary increases in distress as they work through the therapy material.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am currently in regular psychological therapy.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ screening
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~screening
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in posttraumatic stress
Secondary study objectives
Alcohol use
Change in anger
Change in anxiety
+9 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Transdiagnostic ICBT Tailored for PSPExperimental Treatment1 Intervention
Therapist-guided, transdiagnostic Internet-delivered cognitive behavioral therapy tailored specifically for Canadian public safety personnel.
Group II: ICBT for PTSD Tailored for PSPExperimental Treatment1 Intervention
Therapist-guided, Internet-delivered cognitive behavioral therapy for PTSD tailored specifically for Canadian public safety personnel.
Find a Location
Who is running the clinical trial?
Government of CanadaOTHER_GOV
12 Previous Clinical Trials
2,317 Total Patients Enrolled
University of ReginaLead Sponsor
56 Previous Clinical Trials
8,946 Total Patients Enrolled
Heather D Hadjistavropoulos, PhDPrincipal InvestigatorUniversity of Regina
6 Previous Clinical Trials
1,362 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I experience symptoms related to past trauma.I am 18 years old or older.I have concerns about receiving cognitive behavioral therapy.I am currently in regular psychological therapy.
Research Study Groups:
This trial has the following groups:- Group 1: ICBT for PTSD Tailored for PSP
- Group 2: Transdiagnostic ICBT Tailored for PSP
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- 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.