Status:
COMPLETED
Effects of Exercise on Abdominal Obesity and Risk Factors for Cardiovascular Disease
Lead Sponsor:
Queen's University
Collaborating Sponsors:
Canadian Institutes of Health Research (CIHR)
Conditions:
Obesity
Metabolic Syndrome
Eligibility:
All Genders
35-60 years
Phase:
NA
Brief Summary
The investigators will randomize abdominally obese men and women at increased health risk to one of the following 4 conditions: 1) No-exercise, wait list controls (C), 2) Low volume, low intensity exe...
Eligibility Criteria
Inclusion
- Men and women between 40 and 60 years of age. The lower age range for men and women is selected to help ensure recruitment of a sample with metabolic syndrome as prevalence of metabolic syndrome is significantly related to age. The selection of 60 years for the upper age range reflects concerns we have randomizing older adults to the high intensity exercise group wherein exercise at 75-80% of maximum may be difficult to achieve, and likely to be associated with increase orthopaedic injury and thus, poor compliance. We also considered lowering the lower age range from 40 to 35 years, but decided against doing so to increase the cost-effectiveness of recruitment (e.g., ensure a higher yield of those with metabolic syndrome).
- Abdominally obese (waist circumference greater than 88 and 102 cm for women and men respectively) and NCEP-ATPIII defined Metabolic Syndrome. Abdominal obesity for non-Caucasians will be determined using values suggested by the International Diabetes Federation.
- Sedentary lifestyle (planned physical activity for the purpose of health one day per week or less).
- Weight stable (± 2 kg) for 6 months prior to the beginning of the study.
- BMI less than 40 kg/m2 (Because a lifestyle-based intervention alone for obesity reduction is ideal for persons with a BMI less than 40 kg/m2).
Exclusion
- Physical impairment which would make the intervention very difficult, or unsafe according to the patient's physician including history of myocardial infarction, stroke, coronary bypass surgery or angioplasty in the last 6 months; peripheral artery disease, unstable angina or ischemia.
- Diabetes.
- Current smokers.
- Alcohol consumption \> 21 drinks per week.
- Plans to move from the area.
- Participating in another research study.
- Clinically judged to be unsuitable for participation or adherence as determined by the participants physician.
- Inability or unwillingness to provide informed consent.
- For women, planned pregnancy in the next year.
Key Trial Info
Start Date :
September 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 1 2013
Estimated Enrollment :
320 Patients enrolled
Trial Details
Trial ID
NCT00955071
Start Date
September 1 2009
End Date
May 1 2013
Last Update
August 2 2013
Active Locations (1)
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1
School of Kinesiology and Health Studies, Queen's University
Kingston, Ontario, Canada, K7L 3N6