Actively Recruiting
Response Variability to Exercise
Led by Robert Ross, PhD · Updated on 2025-03-20
200
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In this proposal, the investigators challenge the assumption that following the physical activity guidelines implies benefit for ALL adults, and that if benefit is not achieved in response to first line therapy, it will be by simply exercising more. Thus, for improving cardiorespiratory fitness and cardiometabolic risk factors, unanswered questions include: 1) To what extent, regardless of increasing exercise intensity or amount, is exercise not associated with benefit? Demonstration of a resistance to benefit through exercise in a substantial number of adults would be a novel and important finding, would counter the assumptions of many if not most health care practitioners, and could have immediate and direct application in all health care settings. 2) To what extent will non-responders to first line therapy (150 min/wk) be required to increase exercise intensity or amount to achieve benefit? 3) To what extent will failure to improve CRF segregate (be associate with) with cardiometabolic risk factors? The investigators propose that adults who remain exercise resistant for improvement in CRF and cardiometabolic risk despite increasing amount or intensity are at high risk of metabolic disease and consequently, are candidates for alternative treatment strategies.
CONDITIONS
Official Title
Response Variability to Exercise
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Sedentary lifestyle with planned physical activity one day per week or less
- Weight stable within plus or minus 2 kilograms for 6 months prior to the study
- Body Mass Index between 20 and 40 kg/m2
You will not qualify if you...
- Physical impairment making exercise difficult or unsafe as advised by a doctor
- Diabetes
- Current smoker
- Plans to move from the area within the next 8 months
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
School of Kinesiology and Health Studies, Queen's University
Kingston, Ontario, Canada, K7L 3N6
Actively Recruiting
Research Team
R
Robert Ross, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
4
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