Examining Perceptions of the 24-Hr Movement Guidelines

Health Behavior Clinical Trial

Official title:

Examining Perceptions and Brand Approaches for the Canadian 24-Hour Movement Guidelines for Adults

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04281615
• Other study ID #: 6027468
• Status: Completed
• Phase: N/A
• Start date: January 20, 2020
• Est. completion date: February 24, 2020

Study information

• Verified date: September 2021
• Source: Queen's University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 247
• Est. completion date: February 24, 2020
• Est. primary completion date: February 24, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 64 Years

Eligibility

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

Related Conditions & MeSH terms

• Health Behavior
• Self Efficacy

Intervention

Other:
• Generic Message
Exposed to four sets of promotional materials hypothesized to increase perceptions of self-efficacy to meet Guidelines.

Locations

Country	Name	City	State
Canada	School of Kinesiology and Health Studies	Kingston	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
Dr. Amy Latimer-Cheung, PhD

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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