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CompletedNCT02527655Updated Sep 20, 2018

The Men on the Move Study

An interventional study of Choice-Based Physical Activity and Active Transportation in Physical Inactivity, Mobility Limitation and Older Men, sponsored by Simon Fraser University. Completed at 1 site in Canada. Open to male participants aged 65 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-09-20.

Sponsored by Simon Fraser University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
58
Allocation
Randomized
Ages
65 Years and older
Sex
Male
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Study summary

The Men on the Move Study is a randomized, controlled, feasibility study designed to address the health problem of physical inactivity in older men.

Read the detailed description

Men on the Move is a randomized, controlled, feasibility study to provide preliminary evidence of feasibility and efficacy for promoting mobility through the uptake of physical activity among men aged 65 years and older who are physically inactive. Specifically, Men on the Move will evaluate the effects of a choice-based physical activity model paired with an active transportation model. The choice-based physical activity model encourages older men to use existing community-based resources to create and implement actions plans for physical activity. It also provides ongoing face-to-face and telephone-based support from trained activity coaches. The active transportation model provides transit passes and active travel planning to promote use of transit and walking to destinations of interest. The feasibility of delivering the intervention will be assessed. Accelerometry and travel diaries will be used to measure the effects of the intervention on physical activity.

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Conditions studied

  • Physical Inactivity
  • Mobility Limitation
  • Older Men

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03

In context

Mobility Limitation

317 studies on the registry are indexed under Mobility Limitation; 97 are open to participants now.

This study's enrollment of 58 is above the median of 46 across 265 interventional studies indexed under Mobility Limitation.

Browse Mobility Limitation studies →

Lead sponsor

Simon Fraser University is the lead sponsor of 29 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
65 Years and older
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  1. 65 years of age and older;
  2. identify as a man;
  3. English speaking; and
  4. demonstrate readiness for physical activity (by the PAR-Q+ questionnaire or a letter of recommendation from their physician)

Exclusion criteria

Exclusion Criteria:

  1. participated in any strength training in the past 3 months;
  2. participated in any aerobic exercise class in the past 3 months;
  3. live in a nursing home or assisted living facility; or
  4. have plans to be out of town for more than 7 days during the 12-week intervention period.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
58 participants (actual)

Study arms

  • Experimental
    Choice-Based Physical Activity and Active Transportation

    Participants will meet one-on-one with an activity coach to develop a choice-based physical activity and active transportation plan based on their interest, abilities, and resources; attend group-based motivational meetings; and receive ongoing support and encouragement for physical activity and active transportation (e.g., telephone-assisted support, community centre and transit passes).

    Behavioral: Choice-Based Physical Activity and Active Transportation

  • No intervention
    Wait-List Control

    Participants will be offered the Choice-Based Physical Activity and Active Transportation intervention after the experimental arm has completed the study.

Interventions

  • BehavioralChoice-Based Physical Activity and Active Transportation
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What researchers measure

Primary outcomes

  1. Feasibility of participant recruitment and retention

    Number of study participants recruited and retained for the 12-week study

    Time frame: 12 weeks

Secondary outcomes

  1. Change from baseline in physical activity as measured by accelerometry at 12 weeks

    Minutes/day

    Time frame: Baseline and 12 weeks

  2. Change from baseline in daily steps as measured by accelerometry at 12 weeks

    steps/day

    Time frame: Baseline and 12 weeks

  3. Change from baseline in physical activity as measured by the CHAMPS questionnaire score at 12 weeks

    Time frame: Baseline and 12 weeks

  4. Change from baseline in active transportation as measured by travel diaries at 12 weeks

    Trip rates (overall, by walking, by transit)

    Time frame: Baseline and 12 weeks

  5. Change from baseline in mobility as measured by the Short Physical Performance Battery (SPPB) score at 12 weeks

    Time frame: Baseline and 12 weeks

  6. Change from baseline in mobility as measured by the Life-Space Assessment score at 12 weeks

    Time frame: Baseline and 12 weeks

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Study locations

1 site
  • Centre for Hip Health and Mobility
    Vancouver, British Columbia V5Z1M9, Canada
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 20, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02527655
Lead sponsor
Simon Fraser University
Collaborators
Canadian Institutes of Health Research (CIHR), Centre for Hip Health and Mobility
Responsible party
Dawn C. Mackey (Assistant Professor, Simon Fraser University) — Principal investigator
First posted
Aug 19, 2015
Start date
Aug 2015
Primary completion
May 2016
Completion
May 2016
Last update
Sep 20, 2018

Study contacts

Dawn C Mackey, PhD
principal investigator · Simon Fraser University
Heather A McKay, PhD
principal investigator · University of British Columbia
Meghan Winters, PhD
principal investigator · Simon Fraser University
Joanie Sims-Gould, PhD
principal investigator · University of British Columbia
Christiane Hoppmann, PhD
principal investigator · University of British Columbia
Alison Phinney, PhD
principal investigator · University of British Columbia
Karim Khan, PhD
principal investigator · University of British Columbia

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2018. You cannot join it, but the record below documents what was studied.

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