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Clinical Trials/NCT02947230
NCT02947230CompletedNot Applicable

Evaluating the Impact of the McMaster Optimal Aging Portal on Knowledge, Behavioural Intentions and Health Behaviours Related to Physical Mobility

McMaster University2 sites in 1 country535 target enrollmentStarted: March 7, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
535
Locations
2
Primary Endpoint
Google analytics

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Investigator)

Eligibility Criteria

Ages
40 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • English-speaking

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Google analytics

Time Frame: 12 weeks

Understanding participant engagement with the Portal and knowledge translation strategies

Website analytics

Time Frame: 12 weeks

Understanding participant engagement with the Portal and knowledge translation strategies

Email analytics

Time Frame: 12 weeks

Understanding participant engagement with the Portal and knowledge translation strategies

Secondary Outcomes

  • Knowledge Questionnaire(12 weeks, 3 months post-intervention)
  • Beliefs Questionnaire(12 weeks, 3 months post-intervention)
  • Intentions Questionnaire(12 weeks, 3 months post-intervention)
  • Manty Preclinical Mobility Disability Scale(12 weeks, 3 months post-intervention)
  • Rapid Assessment of Physical Activity(12 weeks, 3 months post-intervention)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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