Impact of Mild or Moderate Physical Activity and Progression of Subclinical Atherosclerosis
NCT ID: NCT02628275
Last Updated: 2023-10-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
129 participants
INTERVENTIONAL
2015-08-31
2022-10-31
Brief Summary
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Detailed Description
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MoMA is a randomized controlled trial to study the effects of two doses of physical activity on subclinical atherosclerosis burden progression; 270 inactive men and women aged 18-40 years without CVD or risk factors will be enrolled. At baseline, risk factors, physical activity level and nutritional habits will be measured through validated questionnaires; blood work and anthropometric parameters measurements will be performed (markers of cardiometabolic risk); fitness level will be assessed through treadmill test and accelerometer; magnetic resonance imaging of carotid atherosclerosis, liver and adipose tissue will be performed.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Control
Continued inactivity
No interventions assigned to this group
Moderate to vigorous physical activity
MVPA (55-90% of maximum heart rate) for 150 min/week (current recommendations)
Moderate to vigorous physical activity
55-90% maximum heart rate for 150min/week (current recommendations)
Light physical activity
LPA (40-55% of maximum heart rate) for 150 min/week
Light physical activity
40-55% maximum heart rate for 150min/week
Interventions
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Moderate to vigorous physical activity
55-90% maximum heart rate for 150min/week (current recommendations)
Light physical activity
40-55% maximum heart rate for 150min/week
Eligibility Criteria
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Inclusion Criteria
* Apparent health defined as 1) no known CVD (coronary, cerebrovascular or peripheral vascular disease), and 2) no known cardiovascular risk factors or cardiovascular medications (hypertension, dyslipidemia, diabetes, active smoking within past year, or clinical obesity defined as body mass index (BMI) ≥ 30kg/m2);
* Signed consent form.
Exclusion Criteria
* Hypertension (participants receiving antihypertensive medications or having blood pressure ≥ 135/85 mmHg);
* Diabetes (participants taking diabetes medication or having plasma HbA1c ≥ 6.5%);
* Postmenopausal women;
* Pregnancy or nursing in the past year or expected in the next two years;
* Contraindications to MRI, as per the standardized IUCPQ MRI screening form;
* Participation in another research study.
18 Years
55 Years
ALL
Yes
Sponsors
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Canadian Institutes of Health Research (CIHR)
OTHER_GOV
Laval University
OTHER
Responsible Party
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Eric Larose, DVM, MD, FRCPC, FCCS, FAHA
Full Professor, Faculty of Medicine
Principal Investigators
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Eric Larose, DVM, MD
Role: PRINCIPAL_INVESTIGATOR
Institut universitaire de cardiologie et de pneumologie de Québec, University Laval
Locations
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Institut universitaire de cardiologie et de pneumologie de Québec - Université Laval
Québec, , Canada
Countries
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Other Identifiers
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CIHR MOP-137079
Identifier Type: -
Identifier Source: org_study_id
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