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).
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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