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Increasing Walking Following Cardiac Rehabilitation

U

University of Alberta

Status and phase

Completed
Phase 3
Phase 2

Conditions

Cardiac Diseases
Walking

Treatments

Device: pedometer

Study type

Interventional

Funder types

Other

Identifiers

NCT00281424
B-080105

Details and patient eligibility

About

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.

Full description

As evidenced by the media attention given to pedometers and recent physical activity promotional efforts focused on pedometers, people seem to think that owning a pedometer will influence activity levels.

However, an examination of a few social cognitive theories produces no theoretical rationale that would support any sustained positive influence of pedometers in the absence of some other conditional factor, such as a behavioural goal or a social support system. We believe that once people determine how many steps their usual routes and daily activity typically amounts to, that the pedometer will no longer be used. We based our contentions on two theories: self efficacy theory (Bandura, 1986;1997) and self-determination theory (Deci & Ryan, 2000).

Enrollment

100 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • patients unable to walk or walking contra-indicated
  • unwilling
  • do not read English

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

control
No Intervention group
Description:
no pedometer
pedometer
Experimental group
Description:
given pedometer
Treatment:
Device: pedometer

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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