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Clinical Trials in China / NCT06491329
Starting soon Not applicable

Effect of Aerobic Interval Training on Atrial Fibrillation Burden

NCT06491329 · tracked via the Priya Life Science China tracker
Sponsor
Navy General Hospital, Beijing
Phase
Not applicable
Started
2024-08-15
Last updated
2024-08-02

Condition(s) studied

Atrial FibrillationCardiac Rehabilitation

Investigational drug(s) / intervention(s)

high-intensity interval trainingmoderate-intensity interval training

high-intensity interval training: high-intensity interval training : 40-50 minutes, patients engage in power cycling with intervals of high-intensity exercise at 75%-100% of VO2peak for 30s-1min, followed by 30s-1min of passive recovery, totaling 15-25 cycles.

moderate-intensity interval training: 40-50 minutes, involves power cycling with 8 minutes of moderate-intensity exercise at 40%-60% of VO2peak followed by 2 minutes of passive recovery, totaling 4 cycles.

Study summary

Atrial fibrillation is the most common arrhythmia, with an increasing incidence and prevalence, significantly increasing the risk of death, stroke, heart failure, cognitive impairment, and dementia, severely impacting the quality of life for patients and burdening society and healthcare systems. In recent years, exercise-based cardiac rehabilitation has gradually become a new approach for the treatment of patients with heart disease. The main research topics include: 1. Changes in atrial fibrillation burden in non-permanent atrial fibrillation patients after 12 weeks of HIIT(high-intensity interval training ) or MIIT (moderate-intensity interval training). 2. Changes in cardiorespiratory fitness, quality of life scores, mental health assessment scores, atrial strain, and left ventricular diastolic function in non-permanent atrial fibrillation patients after 12 weeks of aerobic interval training, along with follow-up on the occurrence of exercise-related adverse events and adverse cardiovascular events during the study period.

Eligibility

Sex
ALL
Min age
18 Years
Max age
74 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age range: 18-74 years; 2. Patients with non-permanent atrial fibrillation; 3. Resting heart rate ≤110 beats/min; 4. No history of receiving a formal exercise prescription within the past six months; 5. Willing to participate in this study, provide written informed consent, and agree to comply with follow-up procedures. Exclusion Criteria: 1. History of myocardial infarction, endocarditis/myocarditis/pericarditis, stroke (ischemic/hemorrhagic), pulmonary embolism, lower extremity venous thrombosis, or cardiac surgery within the past 6 months; 2. Moderate to severe pulmonary arterial hypertension, moderate to severe valvular heart disease, hypertrophic cardiomyopathy, aortic stenosis/dilation/dissection/intramural hematoma, congenital heart disease; 3. Heart failure (NYHA class III-IV) or acute exacerbation of heart failure within the past 3 months; 4. Unstable angina or severe coronary artery disease without revascularization; 5. Concurrent severe arrhythmias * frequent multifocal premature ventricular contractions * ventricular tachycardia, ventricular fibrillation * high-degree or complete atrioventricular block * ventricular asystole lasting more than 5 seconds 6. Uncontrolled hypertension or hypotension; 7. Severe renal or hepatic dysfunction * Stage 5 chronic kidney disease, defined as glomerular filtration rate \<15 ml/(min•1.73 m2) or requiring dialysis; * Patient with alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels greater than or equal to 5 times the upper limit of normal as defined by the center during screening; 8. Hypoxemia or severe lung disease; 9. Lower extremity arterial stenosis or musculoskeletal disease preventing exercise training; 10. Intracardiac thrombus; 11. Pregnancy; 12. Cognitive impairment preventing study cooperation; 13. Severe anemia, infection, electrolyte disturbances, hyperthyroidism; 14. Planned atrial fibrillation ablation during the study period; 15. Post-implantation of pacemaker or ICD; 16. Inability to use smart devices; 17. Concurrent cancer or autoimmune or systemic inflammatory disease; 18. Regular moderate-to-high intensity exercise habits (≥2 sessions of high-intensity endurance training per week or ≥3 sessions of moderate-intensity endurance training

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sixth Medical Center of Chinese PLA General Hospital Beijing Beijing Municipality

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06491329 on ClinicalTrials.gov ↗ ← All trials in China