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Cognitive Behavioral Therapy

Internet-Delivered Cognitive Behavioural Therapy for Mental Health Conditions

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
endorsing symptoms of anxiety, depression, or post-traumatic stress
18 years of age or older
Timeline
Screening 3 weeks
Treatment Varies
Follow Up screening
Awards & highlights

Study Summary

This trial looks at whether a cognitive behavioural therapy intervention tailored for Canadian public safety personnel can help with symptoms of depression, anxiety, or posttraumatic stress.

Who is the study for?
This trial is for Canadian public safety personnel in Saskatchewan or Quebec who are over 18 and experiencing symptoms of depression, anxiety, or post-traumatic stress. Participants must have internet access and be willing to name a physician for emergencies.Check my eligibility
What is being tested?
The study tests an Internet-delivered cognitive behavioural therapy (ICBT) program tailored for those with psychological trauma, depression, and anxiety. It measures how well participants engage with the course and any changes in their mental health.See study design
What are the potential side effects?
Since this is a therapy-based intervention rather than medication, traditional side effects are not expected. However, some individuals may experience discomfort when confronting difficult emotions or memories during therapy.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I experience symptoms of anxiety, depression, or PTSD.
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I am 18 years old or older.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~screening and 1, 2, 3, 4, 5, 6, 7, 8, 12, 16, 26, and 52 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and screening and 1, 2, 3, 4, 5, 6, 7, 8, 12, 16, 26, and 52 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
Change in anxiety
Mental Depression
Change in posttraumatic stress
Secondary outcome measures
Alcohol use
Change in anger
Change in functioning
+13 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: Tailored ICBT for PSPExperimental Treatment1 Intervention
Therapist-guided, Internet-delivered cognitive behavioral therapy tailored specifically for Canadian public safety personnel.

Find a Location

Who is running the clinical trial?

University of ReginaLead Sponsor
48 Previous Clinical Trials
7,518 Total Patients Enrolled
Government of CanadaOTHER_GOV
12 Previous Clinical Trials
2,117 Total Patients Enrolled
Heather D Hadjistavropoulos, PhDPrincipal InvestigatorUniversity of Regina
5 Previous Clinical Trials
1,106 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

How many individuals are enrolled in this research endeavor?

"Yes, according to information available on clinicaltrials.gov this trial is still open for enrollment. It was first posted on the 1st of December 2019 and last updated on the 1st of September 2022. Currently 250 individuals are required from a single medical centre."

Answered by AI

Are additional participants being sought for this research endeavor?

"Affirmative. The details of this medical trial, which were first posted on December 1st 2019, are available through clinicaltrials.gov and it is currently enrolling participants. It seeks to recruit 250 people from a single site."

Answered by AI

What is the purport of this research?

"The objective of this clinical research, which will be evaluated throughout a series of timeframes from 1 to 52 weeks, is to determine the impact on post-traumatic stress. Secondary goals include measuring changes in anger using DAR-5 scale (0 - 20), evaluating working alliance with WAI-SR score (4 -20) and monitoring panic symptoms through PDSS rating system (0 - 28). These metrics are only applicable for patients still partaking at week 16."

Answered by AI
~48 spots leftby Mar 2025