[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100553841":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":32,"centralContacts":37,"locations":43,"responsibleParty":56,"collaborators":23,"id":58,"slug":59,"hasResults":60,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":23,"eligibilityCriteria":64,"healthyVolunteers":60,"sex":65,"minAge":66,"maxAge":67,"enrollmentInfo":68,"targetDuration":23,"studyType":71,"phases":72,"briefSummary":74,"conditions":75,"keywords":23,"overallStatus":78,"whyStopped":23,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},{"fullName":5,"class":6},"Navy General Hospital, Beijing","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"High-intensity interval training","EXPERIMENTAL","For non-permanent atrial fibrillation patients, a 12-week high-intensity interval training will be administered. The primary objective is to assess alterations in atrial fibrillation burden, with secondary endpoints encompassing changes in cardiorespiratory fitness, quality of life metrics, psychological profiling, atrial strain, ventricular diastolic function, as well as the incidence rates of exercise-related adverse events and adverse cardiovascular events.",[13],"Other: high-intensity interval training",{"label":15,"type":10,"description":16,"interventionNames":17},"moderate-intensity interval training","For non-permanent atrial fibrillation patients, a 12-week moderate-intensity interval training will be administered. The primary objective is to assess alterations in atrial fibrillation burden, with secondary endpoints encompassing changes in cardiorespiratory fitness, quality of life metrics, psychological profiling, atrial strain, ventricular diastolic function, as well as the incidence rates of exercise-related adverse events and adverse cardiovascular events.",[18],"Other: moderate-intensity interval training",{"label":20,"type":21,"description":22,"interventionNames":23},"Maintain previous exercise habits group","NO_INTERVENTION","Not undergoing exercise rehabilitation, maintaining previous exercise habits",null,[25,29],{"type":6,"name":26,"description":27,"armGroupLabels":28,"otherNames":23},"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.",[9],{"type":6,"name":15,"description":30,"armGroupLabels":31,"otherNames":23},"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.",[15],[33],{"name":34,"affiliation":35,"role":36},"YU-TAO GUO, Doctor","Sixth Medical Center of Chinese PLA General Hospital","STUDY_CHAIR",[38],{"name":39,"role":40,"phone":41,"phoneExt":23,"email":42},"Hui Zhang","CONTACT","8613683176151","zhanghuiay08@sina.com",[44],{"facility":35,"status":23,"city":45,"state":46,"zip":47,"country":48,"countryCode":49,"cosmosGeoPoint":50,"geoPoint":55,"contacts":23},"Beijing","Beijing Municipality","100048","China","CN",{"type":51,"coordinates":52},"Point",[53,54],116.39723,39.9075,{"lat":54,"lon":53},{"type":57,"investigatorFullName":23,"investigatorTitle":23,"investigatorAffiliation":23,"oldNameTitle":23,"oldOrganization":23},"SPONSOR","100553841","effect-of-aerobic-interval-training-on-atrial-fibrillation-burden-100553841",false,"NCT06491329","Effect of Aerobic Interval Training on Atrial Fibrillation Burden","Effect of Aerobic Interval Training on Atrial Fibrillation Burden：A Multicenter Randomized Controlled Study","Inclusion Criteria:\n\n1. Age range: 18-74 years;\n2. Patients with non-permanent atrial fibrillation;\n3. Resting heart rate ≤110 beats\u002Fmin;\n4. No history of receiving a formal exercise prescription within the past six months;\n5. Willing to participate in this study, provide written informed consent, and agree to comply with follow-up procedures.\n\nExclusion Criteria:\n\n1. History of myocardial infarction, endocarditis\u002Fmyocarditis\u002Fpericarditis, stroke (ischemic\u002Fhemorrhagic), pulmonary embolism, lower extremity venous thrombosis, or cardiac surgery within the past 6 months;\n2. Moderate to severe pulmonary arterial hypertension, moderate to severe valvular heart disease, hypertrophic cardiomyopathy, aortic stenosis\u002Fdilation\u002Fdissection\u002Fintramural hematoma, congenital heart disease;\n3. Heart failure (NYHA class III-IV) or acute exacerbation of heart failure within the past 3 months;\n4. Unstable angina or severe coronary artery disease without revascularization;\n5. Concurrent severe arrhythmias\n\n   * frequent multifocal premature ventricular contractions\n   * ventricular tachycardia, ventricular fibrillation\n   * high-degree or complete atrioventricular block\n   * ventricular asystole lasting more than 5 seconds\n6. Uncontrolled hypertension or hypotension;\n7. Severe renal or hepatic dysfunction\n\n   * Stage 5 chronic kidney disease, defined as glomerular filtration rate \\\u003C15 ml\u002F(min•1.73 m2) or requiring dialysis;\n   * 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;\n8. Hypoxemia or severe lung disease;\n9. Lower extremity arterial stenosis or musculoskeletal disease preventing exercise training;\n10. Intracardiac thrombus;\n11. Pregnancy;\n12. Cognitive impairment preventing study cooperation;\n13. Severe anemia, infection, electrolyte disturbances, hyperthyroidism;\n14. Planned atrial fibrillation ablation during the study period;\n15. Post-implantation of pacemaker or ICD;\n16. Inability to use smart devices;\n17. Concurrent cancer or autoimmune or systemic inflammatory disease;\n18. Regular moderate-to-high intensity exercise habits (≥2 sessions of high-intensity endurance training per week or ≥3 sessions of moderate-intensity endurance training","ALL","18 Years","74 Years",{"count":69,"type":70},156,"ESTIMATED","INTERVENTIONAL",[73],"NA","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.",[76,77],"Atrial Fibrillation","Cardiac Rehabilitation","NOT_YET_RECRUITING","2024-08-01",{"date":81,"type":82},"2024-08-02","ACTUAL",{"date":84,"type":70},"2024-08-15",{"date":86,"type":70},"2028-07-30",{"name":5,"class":6},1]