Internet-Delivered Cognitive Behavior Therapy for Anxiety and Depression Amongst French Canadians
Primary Purpose
Major Depression, Anxiety Disorders
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
The Wellbeing Course
Sponsored by

About this trial
This is an interventional treatment trial for Major Depression
Eligibility Criteria
Inclusion Criteria:
- Residing in New-Brunswick, Nova-Scotia, Prince Edward Island, or Newfound land & Labrador
- Having identified French as the first official language spoken and having good reading comprehension in French.
- Reliable Internet access
- Clinically significant levels of depression or anxiety reflected by significant scores on the following measures: PHQ-9 > 9, GAD-7 >7, Penn Stage Worry Questionnaire ≥ 45, Social Phobia Inventory ≥ 19, Panic and Agoraphobia Scale ≥ 19, or by answering yes to the question "Is anxiety or low mood a problem for you"
- Not currently participating in cognitive-behavioral therapy
- No changes in medication for 4 weeks prior to the study, nor any changes in medication for the next 2 months
- Willing to disclose personal information
Exclusion Criteria:
- Presence of psychotic symptoms
- Presence of severe depression as indicated by scores ≥ 23 on the PHQ-9, or a score > 2 on item 9 of the PHQ-9
Sites / Locations
- Université de Moncton - Adult Clinical Psychology Laboratory
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Wellbeing Course
Waitlist-control
Arm Description
Will receive the French-Canadian version of the Wellbeing Course consisting of five lessons based on cognitive behavior therapy delivered through the Internet over eight weeks.
The Waitlist Control Group will receive the French-Canadian version of the Wellbeing Course once the treatment group will have completed treatment.
Outcomes
Primary Outcome Measures
Changes in depression as assessed by the Patient Health Questionnaire-9 (PHQ-9)
Symptoms of depression
Changes in anxiety as assessed by the Generalized Anxiety Disorder-7 (GAD-7)
Symptoms of anxiety
Secondary Outcome Measures
Changes in life satisfaction as assessed by the Satisfaction with Life Scale (SWLS)
Life satisfaction as assessed by the SWLS (Diener et al.,1995)
Changes in health as assessed by the Short-Form Health Survey
Physical and mental health as assessed by the Short-Form Health Survey (SF-12; Ware et al., 1998)
Changes in personality as assessed by the Self-administered Standardised Assessment of Personality - Abbreviated Scale
Pathological personality traits as assessed by the Self-administered Standardised Assessment of Personality - Abbreviated Scale (SAPAS)
Changes in anxiety as assessed by the Penn State Worry Questionnaire (PSWQ)
Symptoms of worry
Changes in social anxiety as assessed by the Social Phobia Inventory (SPIN)
Symptoms of social anxiety symptoms
Changes in panic and agoraphobia as assessed by the Panic and Agoraphobia Scale (PAS)
frequency and intensity of panic symptoms
Full Information
NCT ID
NCT03043833
First Posted
January 30, 2017
Last Updated
April 30, 2018
Sponsor
Universite de Moncton
Collaborators
Macquarie University, Australia
1. Study Identification
Unique Protocol Identification Number
NCT03043833
Brief Title
Internet-Delivered Cognitive Behavior Therapy for Anxiety and Depression Amongst French Canadians
Official Title
Improving Access to Treatment for Anxiety and Depression Among French Canadians Using an Internet-Delivered Cognitive Behavior Therapy: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
January 18, 2017 (Actual)
Primary Completion Date
January 30, 2018 (Actual)
Study Completion Date
March 30, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universite de Moncton
Collaborators
Macquarie University, Australia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study represents Phase II of a research program involving an international collaboration with Macquarie University (Sydney, Australia) to implement an Internet-based cognitive behavior therapy for the treatment of anxiety and depression in French-speaking Canadians from the Atlantic Provinces.
The primary objective is to establish the clinical efficacy of a French-Canadian self-guided format version of the Wellbeing Course by conducting a randomized-control trial where an experimental group will be compared to a waitlist control group. A secondary objective is to demonstrate the course's acceptability through participants' satisfaction with the course.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depression, Anxiety Disorders
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
64 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Wellbeing Course
Arm Type
Experimental
Arm Description
Will receive the French-Canadian version of the Wellbeing Course consisting of five lessons based on cognitive behavior therapy delivered through the Internet over eight weeks.
Arm Title
Waitlist-control
Arm Type
No Intervention
Arm Description
The Waitlist Control Group will receive the French-Canadian version of the Wellbeing Course once the treatment group will have completed treatment.
Intervention Type
Behavioral
Intervention Name(s)
The Wellbeing Course
Intervention Description
The Wellbeing Course (Titov et al., 2011) includes five online lessons:
Lesson 1 presents information on the prevalence of anxiety disorders and depression as well as on how they may interfere with life goals. This lesson also discusses how cognitive, behavioral and physical symptoms can contribute to poor emotional health.
Lesson 2 presents different strategies to generate realistic cognitions.
Lesson 3 describes strategies for physical de-arousal and for re-engaging in reinforcing activities.
Lesson 4 describes avoidance and safety behaviors in relation with anxiety and depression along with graded exposure.
Lesson 5 is about problem solving, relapse prevention and staying well.
For each lesson, a "Do It Yourself" guide is included as well vignettes and additional material.
Primary Outcome Measure Information:
Title
Changes in depression as assessed by the Patient Health Questionnaire-9 (PHQ-9)
Description
Symptoms of depression
Time Frame
Pretest, posttest (week 8), 3-month follow-up
Title
Changes in anxiety as assessed by the Generalized Anxiety Disorder-7 (GAD-7)
Description
Symptoms of anxiety
Time Frame
Pretest, posttest (week 8), 3-month follow-up
Secondary Outcome Measure Information:
Title
Changes in life satisfaction as assessed by the Satisfaction with Life Scale (SWLS)
Description
Life satisfaction as assessed by the SWLS (Diener et al.,1995)
Time Frame
Pretest, posttest (week 8), 3-month follow-up
Title
Changes in health as assessed by the Short-Form Health Survey
Description
Physical and mental health as assessed by the Short-Form Health Survey (SF-12; Ware et al., 1998)
Time Frame
Pretest (week 1), posttest (week 8), 3-month follow-up
Title
Changes in personality as assessed by the Self-administered Standardised Assessment of Personality - Abbreviated Scale
Description
Pathological personality traits as assessed by the Self-administered Standardised Assessment of Personality - Abbreviated Scale (SAPAS)
Time Frame
Pretest (week 1), posttest (week 8), 3-month follow-up
Title
Changes in anxiety as assessed by the Penn State Worry Questionnaire (PSWQ)
Description
Symptoms of worry
Time Frame
Pretest (week 1), posttest (week 8), 3-month follow-up
Title
Changes in social anxiety as assessed by the Social Phobia Inventory (SPIN)
Description
Symptoms of social anxiety symptoms
Time Frame
Pretest (week 1), posttest (week 8), 3-month follow-up
Title
Changes in panic and agoraphobia as assessed by the Panic and Agoraphobia Scale (PAS)
Description
frequency and intensity of panic symptoms
Time Frame
Pretest (week 1), posttest (week 8), 3-month follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Residing in New-Brunswick, Nova-Scotia, Prince Edward Island, or Newfound land & Labrador
Having identified French as the first official language spoken and having good reading comprehension in French.
Reliable Internet access
Clinically significant levels of depression or anxiety reflected by significant scores on the following measures: PHQ-9 > 9, GAD-7 >7, Penn Stage Worry Questionnaire ≥ 45, Social Phobia Inventory ≥ 19, Panic and Agoraphobia Scale ≥ 19, or by answering yes to the question "Is anxiety or low mood a problem for you"
Not currently participating in cognitive-behavioral therapy
No changes in medication for 4 weeks prior to the study, nor any changes in medication for the next 2 months
Willing to disclose personal information
Exclusion Criteria:
Presence of psychotic symptoms
Presence of severe depression as indicated by scores ≥ 23 on the PHQ-9, or a score > 2 on item 9 of the PHQ-9
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
France Talbot, Ph.D.
Organizational Affiliation
Université de Moncton
Official's Role
Study Director
Facility Information:
Facility Name
Université de Moncton - Adult Clinical Psychology Laboratory
City
Moncton
State/Province
New Brunswick
ZIP/Postal Code
E1A 3E9
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
Undecided
IPD Sharing Plan Description
There is currently in place a memorandum of understanding with Macquarie University, our collaborators. This agreement allows for the sharing of data once personally identifiable information has been removed.
Learn more about this trial
Internet-Delivered Cognitive Behavior Therapy for Anxiety and Depression Amongst French Canadians
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