RecruitingNot ApplicableNCT03397602

Exercise Training in Patients With Persistent or Permanent Atrial Fibrillation

Exercise Training in Patients With Persistent or Permanent Atrial Fibrillation - a Multi-centre Randomized Controlled Trial


Sponsor

Ottawa Heart Institute Research Corporation

Enrollment

132 participants

Start Date

Jan 23, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

The main purpose of this project is to evaluate the effects of high-intensity interval training (HIIT) compared to moderate-intensity continuous exercise training (MICE) and standard care on exercise capacity and quality of life in patients with persistent or permanent atrial fibrillation. Positive findings are vitally important for these patients, given the condition's substantial morbidity, mortality and high economic costs.


Eligibility

Min Age: 40 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing whether a supervised exercise training program can improve heart pumping efficiency and quality of life in patients who have persistent or permanent atrial fibrillation — a chronic irregular heartbeat that has not returned to normal on its own. **You may be eligible if...** - You have persistent or permanent atrial fibrillation - Your heart rate at rest is controlled (100 beats per minute or fewer) - You are able to perform a supervised exercise test - You are 40 years old or older **You may NOT be eligible if...** - You already do regular exercise training more than twice per week - You have unstable chest pain (unstable angina) - You have been diagnosed with severe narrowing of the mitral or aortic heart valves - You have a thickened heart muscle causing significant obstruction of blood flow (hypertrophic obstructive cardiomyopathy) - You are pregnant, breastfeeding, or planning to become pregnant during the study Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BEHAVIORALstandard care + moderate-intensity continuous exercise training

Participants will attend on-site moderate-intensity continuous exercise training two times weekly for 12 weeks.

BEHAVIORALstandard care + high-intensity interval training

Participants will attend on-site high-intensity interval training two times weekly for 12 weeks.


Locations(2)

London Health Sciences Network

London, Ontario, Canada

University of Ottawa Heart Insititue

Ottawa, Ontario, Canada

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT03397602


Related Trials