- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00281385
Health and Psychological Outcomes of Lifestyle Versus Traditional Physical Activity
October 10, 2006 updated by: University of Alberta, Physical Education
Health and Psychological Outcomes of Lifestyle Versus Traditional Physical Activity- Study 1
This study is a comparison of the traditional prescription versus the lifestyle exercise prescription in sedentary adults over 6 months.
Biological and psychological parameters will be assessed over the 6 month study.
Biological indicators will be assessed pre and post including body composition, muscular strength, endurance, and flexibility, aerobic fitness, and blood tests.
Psychological parameters will be assessed pre, mid, and post including self-efficacy, motivation, need satisfaction, physical self-description, leisure-time exercise, as well as all constructs from the thepry of planned behaviour.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment
300
Phase
- Phase 2
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Alberta
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Edmonton, Alberta, Canada, t6g 2h9
- University of Alberta
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
25 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 25-65 years old
- exercise less than twice per month in the preceeding 6 months
- physician consent to participate
Exclusion Criteria:
- health problems
- exercise more than twice per month in the preceeding 6 months
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Kerry Courneya, PhD, University of Alberta
- Principal Investigator: Gordon J Bell, PhD, University of Alberta
- Principal Investigator: Vicki J Harber, PhD, University of Alberta
- Principal Investigator: Wendy M Rodgers, PhD., University of Alberta
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
January 20, 2006
First Submitted That Met QC Criteria
January 20, 2006
First Posted (Estimate)
January 24, 2006
Study Record Updates
Last Update Posted (Estimate)
October 11, 2006
Last Update Submitted That Met QC Criteria
October 10, 2006
Last Verified
January 1, 2006
More Information
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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