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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01368172
Other study ID # HicksPAGs
Secondary ID
Status Completed
Phase Phase 1
First received June 6, 2011
Last updated April 7, 2014
Start date July 2011
Est. completion date June 2013

Study information

Verified date April 2014
Source McMaster University
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The first evidence-based physical activity guidelines for people with spinal cord injury were released in March, 2011. This project will evaluate the implementation of the new physical activity guidelines in a community exercise setting in Hamilton, Ontario. The investigators hypothesize that persons who follow the guidelines will experience increased aerobic fitness and muscle strength. The investigators also hypothesize that participants will find the guidelines easy to follow and that their self-efficacy for participating in physical activity will be improved following the study period.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 2013
Est. primary completion date June 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- adults with spinal cord injury who have been given clearance to exercise by their primary care physician (or healthcare team)

Exclusion Criteria:

- ventilatory support

- inability to voluntarily participate in upper body exercises

- inability to communicate in English

- ongoing infection

- unstable autonomic dysreflexia

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Behavioral:
Physical Activity Guidelines
Participants in the Physical Activity Guidelines Arm will be asked to participate in at least 20 minutes of moderate to heavy intensity aerobic activity 2 times per week as well as strength training exercises (moderate intensity) 2 times per week. The Control Arm will not be supervised to follow the physical activity guidelines

Locations

Country Name City State
Canada Centre for Health Promotion and Rehabilitation, McMaster University Hamilton Ontario

Sponsors (2)

Lead Sponsor Collaborator
McMaster University Rick Hansen Foundation

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Physical Fitness Peak VO2 tests will be done on a cycle ergometer to assess aerobic capacity/endurance, and peak strength will be measured on accessible weight-training equipment. 4 months No
Secondary Self-efficacy for achieving the physical activity guidelines Assessed through questionnaire. 4 months No
Secondary Adherence to physical activity guidelines Assessed through enrolment records 4 months No
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