To conduct a randomized control trial to determine the feasibility and preliminary efficacy of a 12-week technology-enabled exercise snacks intervention with behaviour change counselling for improving cardiorespiratory fitness and various markers of cardiometabolic health in previously inactive adults living with obesity.
Age range
35 Years – 64 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Determine the number of individuals living with obesity that are eligible to participate in the trial
Timeframe: through study completion, an average of 18 months
Determine the number of eligible participants who would be willing to take part in this trial
Timeframe: through study completion, an average of 18 months
Determine the number and percentage of participants retained after the 12-week intervention
Timeframe: after the 12-week intervention
Determine the number of one-minute exercise bouts performed during the 12-week intervention
Timeframe: during the 12 weeks