Evaluating the Impact of the McMaster Optimal Aging Portal on Physical Mobility Outcomes

Not Applicable

Completed

• Conditions: Mobility Limitation
• Interventions: Other: Tailored Knowledge Translation

• Registration Number: NCT02947230
• Lead Sponsor: McMaster University

Brief Summary

The McMaster Optimal Aging Portal (the Portal) was launched in 2014 to increase public access to trustworthy health information. The Portal helps readers to access evidence-based resources; identify trustworthy messages; and understand scientific findings. Now the investigators want to know whether using the Portal changes what people know and do to stay healthy and mobile.

This project will help us to:

1. Understand how middle aged and older adults (age 40+) use the Portal to obtain information about maintaining and improving mobility

2. Evaluate whether use of the Portal results in a change in knowledge about maintaining and improving mobility, or change in lifestyle behaviours that may help maintain or improve mobility with age.

Detailed Description

Physically active lifestyles are important for health aging, but most Canadians do not meet published physical activity guidelines. This may be in part due to lack of access to evidence-based information on mobility and aging, and knowledge of strategies to maintain or improve mobility with age. The McMaster Optimal Aging Portal (the Portal) was launched in 2014 to increase public access to trustworthy health information. Now the investigators want to know if easy-to-understand evidence-based messages change what people know and do to stay healthy and mobile.

Sequential, explanatory mixed-methods design consisting of a two-armed randomized controlled trial and a qualitative process study to explore quantitative findings in depth.

Consent forms and a baseline survey will be sent to all interested participants. Following baseline data collection, participants will be stratified by previous Portal use, and randomized to the Knowledge Translation (KT) intervention or control group. During the 12-week KT intervention, intervention group participants will have access to the Portal and will receive mobility- focused weekly email alerts including blog posts and evidence summaries relevant to mobility and be invited to follow a Twitter and Facebook feed; a unique hashtag will be created to identify and collate relevant mobility information. Control group participants will be able to access the Portal in a 'self-serve' fashion, but will not receive targeted KT strategies.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2016-10-21
• Study First Submitted QC: 2016-10-26
• Study First Posted: 2016-10-27
• Study Start: 2017-03-07
• Primary Completion: 2017-11-01
• Study Completion: 2018-12-31
• Status Verified: 2019-03
• Last Update Submitted: 2020-02-19
• Last Update Posted: 2020-02-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 535

Inclusion Criteria

• English-speaking

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Exclusion Criteria

• None

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Tailored Knowledge Translation	Tailored Knowledge Translation	During the 12-week KT intervention, intervention group participants will have access to the Portal and will receive mobility-focused weekly email alerts including blog posts and evidence summaries relevant to mobility and be invited to follow a Twitter and Facebook feed; a unique hashtag will be created to identify and collate relevant mobility information.

Primary Outcome Measures

Name	Time	Method
Google analytics	12 weeks	Understanding participant engagement with the Portal and knowledge translation strategies
Website analytics	12 weeks	Understanding participant engagement with the Portal and knowledge translation strategies
Email analytics	12 weeks	Understanding participant engagement with the Portal and knowledge translation strategies

Secondary Outcome Measures

Name	Time	Method
Knowledge Questionnaire	12 weeks, 3 months post-intervention	Participants knowledge of mobility recommendations and guidelines
Beliefs Questionnaire	12 weeks, 3 months post-intervention	Participants beliefs about the importance of maintaining and improving mobility for health
Intentions Questionnaire	12 weeks, 3 months post-intervention	Participants intentions to engage in lifestyle behaviours related to maintaining or improving mobility
Manty Preclinical Mobility Disability Scale	12 weeks, 3 months post-intervention	Mobility limitation
Rapid Assessment of Physical Activity	12 weeks, 3 months post-intervention	To quantify self-reported physical activity

Trial Locations

Locations (1)

McMaster University; 🇨🇦 Hamilton, Ontario, Canada