Examining Perceptions of the 24-Hr Movement Guidelines

• Sponsor: Dr. Amy Latimer-Cheung, PhD (Other)
• Overall Status: Completed
• CT.gov ID: NCT04281615
• Collaborator: (none)
• Enrollment: 247
• Location: 1
• Arms: 2
• Actual Duration (Months): 1.1
• Patients Per Site Per Month: 214.8

Study Details

Study Description

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.

Condition or Disease	Intervention/Treatment	Phase
Health Behavior; Self Efficacy	Other: Generic Message	N/A

Study Design

• Study Type: Interventional
• Actual Enrollment: 247 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: None (Open Label)
• Primary Purpose: Other
• Official Title: Examining Perceptions and Brand Approaches for the Canadian 24-Hour Movement Guidelines for Adults
• Actual Study Start Date: Jan 20, 2020
• Actual Primary Completion Date: Feb 24, 2020
• Actual Study Completion Date: Feb 24, 2020

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Intervention (Generic Message) Receives promotional materials that feature a generic messaging approach.	Other: Generic Message; 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.

Outcome Measures

Primary Outcome Measures

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]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 64 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	School of Kinesiology and Health Studies	Kingston	Ontario	Canada	K7L3N6

Sponsors and Collaborators

• Dr. Amy Latimer-Cheung, PhD

Investigators

• Principal Investigator: Amy E Latimer-Cheung, PhD, Queen's University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Dr. Amy Latimer-Cheung, PhD, Professor, Queen's University
• ClinicalTrials.gov Identifier: NCT04281615
• Other Study ID Numbers: 6027468
• First Posted: Feb 24, 2020
• Last Update Posted: Sep 30, 2021
• Last Verified: Sep 1, 2021

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Dr. Amy Latimer-Cheung, PhD, Professor, Queen's University: Movement Behaviors; Physical Activity; Sedentary Behaviour; Sleep; Knowledge Translation

Study Results

No Results Posted as of Sep 30, 2021