- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05333627
Internet-delivered Cognitive Behaviour Therapy for Students: Duration Preference Trial
Internet-delivered Cognitive Behaviour Therapy for Post-Secondary Students: Preference Trial for Flexible, 5-Week, and 8-Week Options
There is growing evidence for the effectiveness of internet-delivered cognitive behaviour therapy (ICBT) for post-secondary students with symptoms of depression and anxiety. In ICBT, clients review structured online content over several weeks to learn strategies and skills to manage their symptoms. Low treatment completion rates remain a concern for post-secondary students, so it is possible that existing treatment protocols do not offer enough flexibility for students' needs and preferences.
This trial will examine students' preferences for different course options (fast-track, 5-week, and 8-week) and compare enrollment, adherence, and outcomes of students who pick each of the three options. In all three options, students will receive optional therapist support, in which the assigned therapist only contacts the student on weeks where the student sends the therapist a message. This trial will help inform the delivery of flexible treatment options for post-secondary students in a routine care setting.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Marcie Nugent, MSW
- Phone Number: 3063372946
- Email: marcie.nugent@uregina.ca
Study Contact Backup
- Name: Heather Hadjistavropoulos, PhD
- Phone Number: 3065855133
- Email: hadjista@uregina.ca
Study Locations
-
-
Saskatchewan
-
Regina, Saskatchewan, Canada, S4S 0A2
- Recruiting
- Online Therapy Unit, University of Regina
-
Contact:
- Marcie Nugent, MSW
- Phone Number: 3063373331
- Email: marcie.nugent@uregina.ca
-
Principal Investigator:
- Heather Hadjistavropoulos, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- registered as a student at a post-secondary institution in Saskatchewan; over the age of 18; endorse symptoms of depression (score of 5 or greater on the PHQ-9) and/or anxiety (score of 5 or greater on the GAD-7); and be able to access computers and the Internet and be comfortable using them
Exclusion Criteria:
- high risk of suicide or hospitalization for mental health in previous 12 months; unmanaged alcohol or drug use problems; severe psychiatric illness that is not managed (e.g. psychosis or mania); or receiving other psychological services more than twice per month
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Fast-Track Course
Clients who select the Fast-Track Course option will receive access to a single ICBT core lesson and Do-It-Yourself guide, followed by three additional Do-It-Yourself guides that they can access in any order.
The content includes examples that are tailored to students' experiences.
Clients have access to diverse additional resources (e.g., managing panic, assertive communication) throughout the course.
Clients will receive up to five weeks of optional therapist support.
|
The core Fast-Track lesson includes information on managing their cycle of symptoms, motivation, and an overview of strategies that can be used to manage symptoms of depression and anxiety.
After the core lesson, clients can access three additional Do-It-Yourself guides that focus on thought challenging, controlled breathing/activity planning, and behavioural activation/relapse prevention.
These materials are able to be accessed out of sequence on a schedule that suits their needs.
With optional therapist support, therapists will respond to any messages that clients send once per week.
Therapists will not message clients on weeks where the client does not send a message.
|
|
Experimental: 5-Week Course
Clients who select the 5-week course will receive access to an ICBT course which consists of four lessons spread across the span of five weeks.
The content includes examples that are tailored to students' experiences.
Clients have access to diverse additional resources (e.g., managing panic, assertive communication) throughout the course.
Clients will receive five weeks of optional therapist support.
|
The 5-week course consists of four lessons that provide psychoeducation about: symptom identification and the cognitive behavioural model, thought monitoring and challenging, controlled breathing and pleasant activity scheduling, graded exposure, and relapse prevention.
With optional therapist support, therapists will respond to any messages that clients send once per week.
Therapists will not message clients on weeks where the client does not send a message.
|
|
Experimental: 8-Week Course
Clients who select the 8-week course will receive access to an ICBT course which consists of five lessons spread across the span of eight weeks.
The content in this course is not student-specific.
Clients have access to diverse additional resources (e.g., managing panic, assertive communication) throughout the course.
Clients will receive eight weeks of optional therapist support.
|
The 8-week course consists of five lessons that provide psychoeducation about: symptom identification and the cognitive behavioural model, thought monitoring and challenging, controlled breathing and pleasant activity scheduling, graded exposure, and relapse prevention.
With optional therapist support, therapists will respond to any messages that clients send once per week.
Therapists will not message clients on weeks where the client does not send a message.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient Health Questionnaire 9-item (PHQ-9)
Time Frame: Baseline (screening), weeks 1-5 (Fast-Track and 5-week course), weeks 1-8 (8-week course), and week 16 (all course options)
|
Change in depression symptoms.
9 items are summed into a total score, with scores ranging from 0 to 27.
Higher scores are associated with higher depression severity.
|
Baseline (screening), weeks 1-5 (Fast-Track and 5-week course), weeks 1-8 (8-week course), and week 16 (all course options)
|
|
Generalized Anxiety Disorder 7-item (GAD-7)
Time Frame: Baseline (screening), weeks 1-5 (Fast-Track and 5-week course), weeks 1-8 (8-week course), and week 16 (all course options)
|
Change in anxiety symptoms.
7 items are summed into a total score ranging from 0 to 21, with higher scores indicating more severe self-reported levels of anxiety.
|
Baseline (screening), weeks 1-5 (Fast-Track and 5-week course), weeks 1-8 (8-week course), and week 16 (all course options)
|
|
Perceptions of Academic Functioning (PAF)
Time Frame: Baseline (screening), weeks 1-5 (Fast-Track and 5-week course), weeks 1-8 (8-week course), and week 16 (all course options)
|
Change in subjective academic functioning.
3 items are summed into a total score ranging from 0 to 30, with higher scores indicating higher perceived functioning.
|
Baseline (screening), weeks 1-5 (Fast-Track and 5-week course), weeks 1-8 (8-week course), and week 16 (all course options)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Credibility and Expectancy Questionnaire (CEQ)
Time Frame: Baseline (screening), week 5 (Fast-Track and 5-week course), week 8 (8-week course)
|
Measure of treatment credibility.
Three items range from 0-9 with higher scores indicating better outcome.
|
Baseline (screening), week 5 (Fast-Track and 5-week course), week 8 (8-week course)
|
|
Treatment Satisfaction
Time Frame: Week 5 (Fast-Track and 5-week course); Week 8 (8-week course)
|
Measure includes 19 questions assessing satisfaction with various aspects of Internet-CBT and also negative effects of treatment
|
Week 5 (Fast-Track and 5-week course); Week 8 (8-week course)
|
|
Work and Social Adjustment Scale (WSAS)
Time Frame: Baseline (screening), week 5 (Fast-Track and 5-week course), week 8 (8-week course)
|
Measure includes 5 questions assessing impairment of functioning.
Items are scored on a scale of 0 to 8. Total scores on the WSAS range from 0 to 40 with higher scores suggesting severe impairment.
|
Baseline (screening), week 5 (Fast-Track and 5-week course), week 8 (8-week course)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Alcohol Use Disorder Identification Test (AUDIT)
Time Frame: Baseline (screening)
|
A 10-item screening tool to assess alcohol consumption.
Items 1 to 8 are scored on a scale ranging from 0 to 4. Items 9 and 10 are scored on a three-point scale (0, 2, or 4).
Scores from 10 items are summed with possible scores ranging from 0 to 40 and higher scores indicating a higher likelihood of problematic alcohol consumption.
|
Baseline (screening)
|
|
Drug Use Disorder Identification Test (DUDIT)
Time Frame: Baseline (screening)
|
An 11-item screening tool to assess problematic drug use.
Items 1 to 9 are scored on a scale ranging from 0 to 4. Items 10 and 11 are scored as a 0, 2, or 4. Total scores for the DUDIT range from 0 to 44 with higher scores suggesting problematic drug use.
|
Baseline (screening)
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Vanessa Peynenburg, MA, University of Regina
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019-205b
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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