Status:

UNKNOWN

Atrial Electromechanical Function in Endurance Athletes With and Without Atrial Fibrillation

Lead Sponsor:

University of Toronto

Collaborating Sponsors:

Unity Health Toronto

Conditions:

Paroxysmal Atrial Fibrillation

Eligibility:

MALE

45-65 years

Brief Summary

This study evaluates cardiac structure and function differences between healthy endurance trained athletes with atrial fibrillation and healthy age matched endurance trained athletes without atrial fi...

Detailed Description

Regular physical activity, including vigorous exercise, lowers cardiovascular risk factors, including the risk of developing Atrial Fibrillation (AF), one of the most commonly diagnosed types of arrhy...

Eligibility Criteria

Inclusion

  • ALL participants:
  • endurance athlete (cyclist, runner, triathlete or other) who participate in vigorous year-round training of 4-6 hours per week for a minimum of 20 years
  • participation in atleast one major competition per year (marathon/triathlon/endurance competition)
  • sinus rhythm during all assessments
  • Inclusion criteria specific to endurance athletes with AF:
  • diagnosed with lone paroxysmal AF in the last 4 years
  • able to verify diagnosis (ECG or Holter verification/proof of diagnosis),
  • can be on any type of medication.
  • Inclusion criteria specific to healthy endurance athletes without AF:
  • previous participation in Athlete's Heart Study
  • has completed resting cardiac magnetic resonance imaging and resting electrocardiogram

Exclusion

  • females
  • no more than \>1 hour per week of resistance training
  • treatment or prior diagnosis of cardiovascular disease, valvular disease, hypertension, heart failure, diabetes, thyroid disorder, sleep apnea, current/recent viral disease, chronic inflammatory disease
  • previous (within 10 years) or current smoking
  • recreational drug use or alcohol consumption in excess of accepted standards
  • inability to provide informed consent
  • inability to verify AF diagnosis (if AF athlete).

Key Trial Info

Start Date :

January 30 2018

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

August 1 2021

Estimated Enrollment :

34 Patients enrolled

Trial Details

Trial ID

NCT03305744

Start Date

January 30 2018

End Date

August 1 2021

Last Update

November 3 2020

Active Locations (1)

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1

Goldring Center for High Performance

Toronto, Ontario, Canada, M5S 2C9