Increasing Walking Following Cardiac Rehabilitation
1 other identifier
interventional
100
1 country
1
Brief Summary
The purpose of the project was to test the widely endorsed assumption that pedometers produce or encourage more physical activity participation in the form of walking. The investigators hypothesized that pedometers would not increase the amount of walking cardiac patients participated in after their cardiac rehabilitation program compared to patients without pedometers.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_2
Started Jun 2005
Typical duration for phase_2
1 active site
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
Study Start
First participant enrolled
June 1, 2005
CompletedFirst Submitted
Initial submission to the registry
January 20, 2006
CompletedFirst Posted
Study publicly available on registry
January 24, 2006
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2009
CompletedNovember 6, 2024
November 1, 2024
2.6 years
January 20, 2006
November 4, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Physical activity behaviour
months
Study Arms (2)
control
NO INTERVENTIONno pedometer
pedometer
EXPERIMENTALgiven pedometer
Interventions
Eligibility Criteria
You may qualify if:
- All patients referred to the Northern Alberta Cardiac Rehabilitation Program
- Patients who are willing to participate
- Are able to read English
- Patients who are able to walk at 2.0 mph based on their exercise stress test results
You may not qualify if:
- patients unable to walk or walking contra-indicated
- unwilling
- do not read English
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Glenrose Rehabilitation Hospital
Edmonton, Alberta, T6H 1X5, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Wendy M Rodgers, PhD
University of Alberta
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 20, 2006
First Posted
January 24, 2006
Study Start
June 1, 2005
Primary Completion
January 1, 2008
Study Completion
January 1, 2009
Last Updated
November 6, 2024
Record last verified: 2024-11
Data Sharing
- IPD Sharing
- Will not share