NCT02527655

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
58

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2015

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 29, 2015

Completed
3 days until next milestone

Study Start

First participant enrolled

August 1, 2015

Completed
18 days until next milestone

First Posted

Study publicly available on registry

August 19, 2015

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2016

Completed
Last Updated

September 20, 2018

Status Verified

February 1, 2018

Enrollment Period

9 months

First QC Date

July 29, 2015

Last Update Submit

September 19, 2018

Conditions

Physical InactivityMobility LimitationOlder Men

Outcome Measures

Primary Outcomes (1)

  • Feasibility of participant recruitment and retention

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

    12 weeks

Secondary Outcomes (6)

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

    Baseline and 12 weeks

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

    Baseline and 12 weeks

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

    Baseline and 12 weeks

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

    Baseline and 12 weeks

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

    Baseline and 12 weeks

  • +1 more secondary outcomes

Study Arms (2)

Choice-Based Physical Activity and Active Transportation

EXPERIMENTAL

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

Wait-List Control

NO INTERVENTION

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

Interventions

Choice-Based Physical Activity and Active TransportationBEHAVIORAL
Choice-Based Physical Activity and Active Transportation

Eligibility Criteria

Age65 Years+
Sexmale
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre for Hip Health and Mobility

Vancouver, British Columbia, V5Z1M9, Canada

Location

MeSH Terms

Conditions

Sedentary BehaviorMobility Limitation

Condition Hierarchy (Ancestors)

BehaviorSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Dawn C Mackey, PhD

    Simon Fraser University

    PRINCIPAL INVESTIGATOR

  • Heather A McKay, PhD

    University of British Columbia

    PRINCIPAL INVESTIGATOR

  • Meghan Winters, PhD

    Simon Fraser University

    PRINCIPAL INVESTIGATOR

  • Joanie Sims-Gould, PhD

    University of British Columbia

    PRINCIPAL INVESTIGATOR

  • Christiane Hoppmann, PhD

    University of British Columbia

    PRINCIPAL INVESTIGATOR

  • Alison Phinney, PhD

    University of British Columbia

    PRINCIPAL INVESTIGATOR

  • Karim Khan, PhD

    University of British Columbia

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

July 29, 2015

First Posted

August 19, 2015

Study Start

August 1, 2015

Primary Completion

May 1, 2016

Study Completion

May 1, 2016

Last Updated

September 20, 2018

Record last verified: 2018-02

Locations

CA(1)