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

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Healthy Volunteers: f
View:

• Paroxysmal and Persistent AF

• Rate controlled (resting ventricular rate \<110 bpm)

• Able to do a symptom limited exercise test

• At least 40 years of age

• Self-reports being symptomatic in the past 4 weeks

• If female, self-reports being post-menopausal

• Able to read and understand English or French

• Agrees to sign informed consent

Locations
Other Locations
Canada
University of Ottawa Heart Institute
RECRUITING
Ottawa
Contact Information
Primary
Matheus Mistura
mmistura@ottawaheart.ca
613-696-7000
Time Frame
Start Date: 2022-02-08
Estimated Completion Date: 2026-04-01
Participants
Target number of participants: 36
Treatments
Experimental: Moderate Intensity Continuous Training (MICT)
Participants will do 3 sessions of moderate-intensity continous exercise training over 7 days
Experimental: High Intensity Interval Training (HIIT)
Participants will do 3 sessions of high-intensity interval training over 7 days
No_intervention: Rest
Participants will abstain from doing moderate- to high-intensity interval training over 7 days
Related Therapeutic Areas
Sponsors
Leads: Ottawa Heart Institute Research Corporation

This content was sourced from clinicaltrials.gov