- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04281615
Examining Perceptions of the 24-Hr Movement Guidelines
September 28, 2021 updated by: Dr. Amy Latimer-Cheung, PhD
Examining Perceptions and Brand Approaches for the Canadian 24-Hour Movement Guidelines for Adults
The main objective of the proposed research is to experimentally test and inform the most effective brand attributes that is to be featured in the forthcoming Canadian 24-Hour Movement Guidelines for Adults.
Specifically, there are two main objectives.
The first objective is to determine the most preferred tagline associated with the new Guidelines among a sample of Canadian adults.
The second objective is to experimentally test if this new attribute fosters stronger perceptions of self-efficacy among an adult sample, when compared to previous threshold-based approaches.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
247
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Kingston, Ontario, Canada, K7L3N6
- School of Kinesiology and Health Studies
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 64 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- between 18-64 years
- Canadian
Exclusion Criteria:
- cannot read/write in English
- already self-reported meeting Guideline recommendations for all three behaviours (physical activity, sedentary behaviour, and sleep)
- self-reported medical condition and/or sleep condition that would prevent individual from meeting the Guideline recommendations
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention (Generic Message)
Receives promotional materials that feature a generic messaging approach.
|
Exposed to four sets of promotional materials hypothesized to increase perceptions of self-efficacy to meet Guidelines.
|
|
No Intervention: Control (Threshold Message)
Receives promotional materials that use traditional, threshold messages.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change in participants self-efficacy to meet Guidelines measured using the Multi-Dimensional Self-efficacy for Exercise Scale (adapted, scale 0-10; 0=not at all confident, 10=extremely confident) following pre and post exposure to promotional materials.
Time Frame: 3 time points: measuring change from baseline, immediately after viewing message, 2-week follow up
|
3 time points: measuring change from baseline, immediately after viewing message, 2-week follow up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Amy E Latimer-Cheung, PhD, Queen's University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 20, 2020
Primary Completion (Actual)
February 24, 2020
Study Completion (Actual)
February 24, 2020
Study Registration Dates
First Submitted
February 18, 2020
First Submitted That Met QC Criteria
February 20, 2020
First Posted (Actual)
February 24, 2020
Study Record Updates
Last Update Posted (Actual)
September 30, 2021
Last Update Submitted That Met QC Criteria
September 28, 2021
Last Verified
September 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 6027468
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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