Examining Perceptions of the 24-Hr Movement Guidelines
Examining Perceptions and Brand Approaches for the Canadian 24-Hour Movement Guidelines for Adults
1 other identifier
interventional
247
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2020
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 20, 2020
CompletedFirst Submitted
Initial submission to the registry
February 18, 2020
CompletedFirst Posted
Study publicly available on registry
February 24, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 24, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
February 24, 2020
CompletedSeptember 30, 2021
September 1, 2021
1 month
February 18, 2020
September 28, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
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.
3 time points: measuring change from baseline, immediately after viewing message, 2-week follow up
Study Arms (2)
Intervention (Generic Message)
EXPERIMENTALReceives promotional materials that feature a generic messaging approach.
Control (Threshold Message)
NO INTERVENTIONReceives promotional materials that use traditional, threshold messages.
Interventions
Exposed to four sets of promotional materials hypothesized to increase perceptions of self-efficacy to meet Guidelines.
Eligibility Criteria
You may qualify if:
- between 18-64 years
- Canadian
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
School of Kinesiology and Health Studies
Kingston, Ontario, K7L3N6, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Amy E Latimer-Cheung, PhD
Queen's University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
February 18, 2020
First Posted
February 24, 2020
Study Start
January 20, 2020
Primary Completion
February 24, 2020
Study Completion
February 24, 2020
Last Updated
September 30, 2021
Record last verified: 2021-09
Data Sharing
- IPD Sharing
- Will not share