Recruiting NA Atrial Fibrillation

New treatment option for Atrial Fibrillation

Official title Exercise Training in Patients With Persistent or Permanent Atrial Fibrillation

ClinicalTrials.gov ID: NCT03397602

What this study is testing

What it's testing
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.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 40 and older

You may be able to join if

  • persistent or permanent atrial fibrillation;
  • rate controlled with a resting ventricular rate of equal to or less than 100 bpm;
  • able to perform a symptom-limited exercise test;
  • at least 40 years of age (i.e. participants must be 40 years or older);

You likely can't join if

  • currently participating in routine exercise training (more than two times per week);
  • unstable angina;
  • diagnosed severe mitral or aortic stenosis;
  • diagnosed hypertrophic obstructive cardiomyopathy with significant obstruction;
  • pregnant, lactating or planning to become pregnant during the study period;
  • unable to provide written, informed consent, or
See the full eligibility criteria
Who can join
  • persistent or permanent atrial fibrillation;
  • rate controlled with a resting ventricular rate of equal to or less than 100 bpm;
  • able to perform a symptom-limited exercise test;
  • at least 40 years of age (i.e. participants must be 40 years or older);
What rules you out
  • currently participating in routine exercise training (more than two times per week);
  • unstable angina;
  • diagnosed severe mitral or aortic stenosis;
  • diagnosed hypertrophic obstructive cardiomyopathy with significant obstruction;
  • pregnant, lactating or planning to become pregnant during the study period;
  • unable to provide written, informed consent, or
  • unwilling or unable to return for follow up at week 12.

The study team makes the final eligibility decision.

Where it's taking place

  • London, Ontario, Canada
  • Ottawa, Ontario, Canada

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 40 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include London, Ontario, Canada; Ottawa, Ontario, Canada. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.