Exercise Training to Atrial Fibrillation

NCT ID: NCT04508478

Last Updated: 2025-08-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-11-03

Study Completion Date

2026-12-31

Brief Summary

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To test the impacts of different exercise training programs to the cardiopulmonary function, muscle metabolism, and body mass composition

Detailed Description

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Atrial fibrillation (AF) has been a global threat due to its increasing incidence and prevalence, and also its potential complications of embolic stroke and heart failure, and therefore has a great impact on life expectancy and quality of life. AF with preserved ventricular function is associated with exercise intolerance, and the effect of physical training had shown to improve life quality and heart function in the population. However, the optimal physical training modalities and intensities are not well studies.

Here we conduct a prospective, randomized, and interventional trial to investigate the effects of different exercise training programs to the burden of AF. We also exploit advanced imaging modalities, including dual x-ray absorptiometry and muscle magnetic resonance, to explore the change of body mass compositions. With this project, we will be able to explore the effects of different physical exercise modalities to the burden of AF and heart function, and also build up a best exercise training program, specific for this population.

Conditions

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Atrial Fibrillation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Aerobic training

Group Type EXPERIMENTAL

Aerobic training

Intervention Type BEHAVIORAL

Aerobic training

Resistance training

Group Type ACTIVE_COMPARATOR

Resistance training

Intervention Type BEHAVIORAL

Resistance training

Control

Group Type PLACEBO_COMPARATOR

Control physical exercise

Intervention Type BEHAVIORAL

Control physical exercise

Interventions

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Aerobic training

Aerobic training

Intervention Type BEHAVIORAL

Resistance training

Resistance training

Intervention Type BEHAVIORAL

Control physical exercise

Control physical exercise

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Paroxysmal or persistent atrial fibrillation
2. Daily activity below moderate intensity \< 300 minutes or high intensity \< 150 minutes per week.

Exclusion Criteria

1. Active infection.
2. Implant cardiac pacemaker.
3. Uncontrolled hypertension.
4. Cardiopulmonary contraindication to exercise training, such as decompensated heart failure, acute pulmonary edema, unstable angina, uncontrolled arrhythmia causing hemodynamic compromise, symptomatic severe aortic stenosis, suspected dissecting aortic aneurysm, severe pulmonary hypertension, acute myocarditis, endocarditis or pericarditis, uncontrolled asthma and SpO2 \< 90% at rest on room air.
5. Inability to follow verbal command or to walk on treadmill or use stationary bike.
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Taiwan University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Chih-Chieh Yu, MD.PhD

Role: PRINCIPAL_INVESTIGATOR

National Taiwan University Hospital

Locations

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National Taiwan University Hospital

Taipei, , Taiwan

Site Status

Countries

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Taiwan

Other Identifiers

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202007030RINC

Identifier Type: -

Identifier Source: org_study_id

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