Acute Responses to Exercise in Females and Males With Symptomatic Atrial Fibrillation
NCT05085860
Summary
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).
Eligibility
Inclusion Criteria: * Paroxysmal and Persistent AF * Rate controlled (resting ventricular rate \<110 bpm) * Able to do a symptom limited exercise test * At least 40 years of age * Self-reports being symptomatic in the past 4 weeks * If female, self-reports being post-menopausal * Able to read and understand English or French * Agrees to sign informed consent Exclusion Criteria: * Currently participating in routine exercise training * Unstable angina or uncontrolled diabetes mellitus; or established diagnosis of severe mitral or aortic stenosis, or hypertrophic obstructive cardiomyopathy with significant obstruction * Unable to access the Internet or a phone (iPhone and iPad require iOS version 10.0 and up, Android requires version 6.0 and up) during the study period * Has an automated external defibrillator, an implantable cardioverter defibrillator or other types of pacemaker * Unwilling or unable to complete the three conditions * Unable to provide written, informed consent
Conditions4
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NCT05085860