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Clinical Trials in Canada / NCT05496751
Recruiting Not applicable

Response Variability to Exercise

NCT05496751 · tracked via the Priya Life Science Canada tracker
Sponsor
Robert Ross, PhD
Phase
Not applicable
Started
2022-09-30
Last updated
2025-03-20

Condition(s) studied

ExerciseCardiorespiratory Fitness

Investigational drug(s) / intervention(s)

Low amount, low intensity exerciseLow amount, high intensity exerciseHigh amount, high intensity exercise

Low amount, low intensity exercise: Participants will exercise under supervision. Exercise dose will vary by amount and intensity

Low amount, high intensity exercise: Participants will exercise under supervision. Exercise dose will vary by amount and intensity

High amount, high intensity exercise: Participants will exercise under supervision. Exercise dose will vary by amount and intensity

Study summary

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.

Eligibility

Sex
ALL
Min age
25 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Sedentary lifestyle (planned physical activity for one day per week or less). * Weight stable (± 2 kg) for 6 months prior to the beginning of the study. * BMI between 20 and 40 kg/m2. Exclusion Criteria: * Physical impairment which would make the intervention very difficult or unsafe according to doctor's advice. * Diabetes, current smokers. * Plan to move from the area in next 8 months.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
School of Kinesiology and Health Studies, Queen's University Kingston Ontario Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05496751 on ClinicalTrials.gov ↗ ← All trials in Canada