- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05772650
The Online Mood Booster Challenge to Support Physical and Mental Health
Healthier Together Mood Booster Challenge
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
An 8-week web-based health promotion program to learn strategies and use digital tools that will give participants a physical, mental, and emotional boost, with exercise remaining a key component of the mission.
Each week participants will learn and practice evidence-based strategies that they will master to improve their physical and mental health.
Techniques will be focused on: spending time exercising outdoors, practicing daily gratitude, practicing good posture, building social connection, deep breathing, listening to music, limiting time on social media and focusing on better sleep.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Dr. Steven Grover, MD
- Phone Number: 223 514-846-7973
- Email: steven.grover@mcgill.ca
Study Contact Backup
- Name: Violette Berberian, B.Sc.., MBA
- Phone Number: 514-715-2827
- Email: violette.berberian@affiliate.mcgill.ca
Study Locations
-
-
Quebec
-
Montreal, Quebec, Canada, H3A 0G4
- Recruiting
- McGill University
-
Contact:
- Dr. Steven Grover, MD
- Phone Number: 514-791-5688
- Email: steven.grover@mcGill.ca
-
Contact:
- Violette Berberian, B.S.C., MBA
- Phone Number: 514-715-2827
- Email: violette.berberian@affiliate.mcgill.ca
-
Principal Investigator:
- Dr. Steven Grover, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Affiliated with McGill University or family member
Exclusion Criteria: None
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improvement in Physical Activity Levels
Time Frame: Feb 20 - April 16, 2023
|
8 week program to create healthy habits of incorporating increased physical activity in daily life. Self-reported physical activity levels using the International Physical Activity Questionnaire (IPAQ) (weekly metabolic equivalents (METs); using an estimate of 4 METs/ min moderate exercise and 8 METs/ min vigorous exercise) |
Feb 20 - April 16, 2023
|
|
Adherence to Program
Time Frame: Feb 20 - April 16, 2023
|
8 Week program to help change behaviour for healthy habit creation. Adherence will be measured as the number of days tracking physical activity levels and answering the behaviour change questions. Less than 7 days = very poor adherence 7-21 days = poor adherence 22-42 days = moderate adherence 43-49 days = good adherence Greater than 49 days = excellent adherence |
Feb 20 - April 16, 2023
|
|
Improvement in Stress
Time Frame: Feb 20 - April 16, 2023
|
The following methodology will be used to measure the above metric: - Stress score - Perceived Stress Scale. 10 questions; Total score from 0 to 40; ≥18 high stress (1 standard deviation above the mean) |
Feb 20 - April 16, 2023
|
|
Improvement in Sleep
Time Frame: Feb 20 - April 16, 2023
|
The following methodology will be used to measure the above metric: - Sleep score - Insomnia Severity Index. 7 questions; Total score from 0 to 28; ≥ 8 subthreshold insomnia |
Feb 20 - April 16, 2023
|
|
Improvement in Mood
Time Frame: Feb 20 - April 16, 2023
|
The following methodology will be used to measure the above metric: - Depression score - Centre for Epidemiological Studies - Depression questionnaire 20 questions; Total score 0-40; ≥16 subthreshold depressive symptoms |
Feb 20 - April 16, 2023
|
|
Improvement in Burnout
Time Frame: Feb 20 - April 16, 2023
|
The following methodology will be used to measure the above metric: - Burnout - Oldenburg burnout assessment. <2.89 no or little sign of burnout; 2.89 to 3.51 may be at risk of burnout; >3.51 at very high risk of burnout |
Feb 20 - April 16, 2023
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Dr. Steven Grover, MD, McGill University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Other Study ID Numbers
- CLIN1903
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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