The main purpose of this pilot project is to measure the feasibility of conducting a randomized crossover study examining short-term changes in atrial fibrillation (AF) symptoms in symptomatic females and males with paroxysmal or persistent AF when they engage in a standard week of exercise (i.e. moderate-intensity continuous training \[MICT\] or high-intensity interval training \[HIIT\]) compared to a control week (i.e. no moderate to vigorous exercise over 7 days).
Age range
40 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.
Feasibility of the pilot study - Recruitment and consent rate
Timeframe: Through study completion, an average of 1.5 years
Feasibility of the pilot study - Participant fidelity
Timeframe: During the week of HIIT and MICT (2 weeks)
Feasibility of the pilot study - Study retention
Timeframe: Through study completion, an average of 1.5 years
Feasibility of the pilot study - Study eligibility refinement
Timeframe: Through study completion, an average of 1.5 years
Feasibility of the pilot study - Adverse events
Timeframe: Through study completion, an average of 1.5 years