Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
ID05085860

Feasibility of Examining Acute Responses to Exercise in Symptomatic Females and Males With Atrial Fibrillation: a Pilot Randomized Crossover Study

Led by Ottawa Heart Institute Research Corporation · Updated on 2026-05-06

36

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying people with symptomatic atrial fibrillation (AF), including both paroxysmal and persistent types, to see how short-term exercise affects their AF symptoms. This pilot randomized crossover study compares symptom changes during a week of moderate-intensity continuous training (MICT) or high-intensity interval training (HIIT) with a week of no moderate to vigorous exercise. The goal is to understand how exercise acutely influences AF symptoms, especially noting differences between females and males. Participants will take part in three different 7-day periods: one with moderate-intensity continuous exercise, one with high-intensity interval training, and one without moderate to vigorous exercise. During each exercise week, participants will complete three exercise sessions. The study uses a wireless four-finger AliveCor KardiaMobile ECG device to monitor AF status daily. Participants also report symptoms using a 7-day questionnaire during each period. Throughout the study, researchers will check how feasible it is to conduct this crossover trial by tracking recruitment, consent, participant adherence, retention, eligibility adjustments, and any adverse events over about 1.5 years. Participants will have their AF symptoms and heart activity monitored closely during each week. The total observation includes three weeks for the exercise and control conditions, with ongoing safety and study progress evaluations.

CONDITIONS

Brief Title

Acute Responses to Exercise in Females and Males With Symptomatic Atrial Fibrillation

Who Can Participate

Age: 40Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of paroxysmal or persistent atrial fibrillation
  • Resting ventricular rate less than 110 beats per minute
  • Able to perform a symptom-limited exercise test
  • At least 40 years of age
  • Self-reported symptoms of atrial fibrillation in the past 4 weeks
  • If female, self-reported post-menopausal status
  • Able to read and understand English or French
  • Willing to sign informed consent
Not Eligible

You will not qualify if you...

  • Currently participating in routine exercise training
  • Unstable angina or uncontrolled diabetes mellitus
  • Severe mitral or aortic stenosis or hypertrophic obstructive cardiomyopathy with significant obstruction
  • Unable to access the Internet or a phone (iOS 10.0+ or Android 6.0+ required) during the study
  • Has an automated external defibrillator, implantable cardioverter defibrillator, or other pacemaker
  • Unwilling or unable to complete all three study conditions
  • Unable to provide written informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 3 weeks (1 week per condition)

Participants will engage in three sessions of moderate-intensity continuous training (MICT), high-intensity interval training (HIIT), or abstain from moderate- to high-intensity exercise over separate 7-day periods to measure acute responses to exercise.

Daily symptom recording and ECG measurements during each 7-day period

Trial Site Locations

Total: 1 location

1

University of Ottawa Heart Institute

Ottawa, Ontario, Canada, K1Y4W7

Actively Recruiting

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Research Team

M

Matheus Mistura

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

3

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