Non-paroxysmal atrial fibrillation
Conditions
Interventions
Conventional treatment + cardiac rehabilitation + intelligent service group:Conventional Treatment Cardiac Rehabilitation Smart Service Group
Conventional treatment group:Conventional treatment
Conventional treatment + cardiac rehabilitation group:Conventional treatment+Cardiac rehabilitation exercise
Sponsors
Tianjin Fourth Central Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1.Meet the diagnostic criteria for persistent atrial fibrillation as stipulated in the "Chinese Guidelines for the Diagnosis and Treatment of Atrial Fibrillation", and be aged between 18 and 75 years old. 2.Be able to communicate normally with medical staff and be willing to accept cardiac rehabilitation treatment; The sports risk levels are classified as moderate risk and low risk. 3.Patients who can receive long-term and regular anticoagulant therapy (warfarin or new oral anticoagulants).
Exclusion criteria
Exclusion criteria: 1.Those who have a history of acute myocardial infarction within one month; 2.For patients with severe malignant arrhythmia and high-grade atrioventricular block without pacemaker treatment; 3.Those with concurrent malignant tumors; 4.Those with impaired functions of vital organs; 5.Uncontrolled hypertension (SBP greater than 200mmHg or DBP greater than 110mmHg); 6.Symptomatic hypertrophic obstructive cardiomyopathy or aortic stenosis; 7.Patients who underwent radiofrequency ablation during the enrollment period; 8.Those who have recently been classified as high-risk due to thromboembolism and exercise risk stratification; 9.Due to various reasons for loss of follow-up or expected survival time, the test criteria were dropped; 10.Patients who have undergone previous heart valve replacement or repair surgeries; 11.Those with a history of severe stroke, cerebral hemorrhage, serious mental illness, cognitive dysfunction or inability to communicate and cooperate; 12.Those who are unable to persist in cardiac rehabilitation training due to adverse events such as acute aggravation of the condition, concurrent other diseases, musculoskeletal events, etc; 13.Subjects may voluntarily decide to withdraw from the trial at any time.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Symptom assessment: Quality of Life Rating Scale (SF-36);Vital sign;6-Minute Walk Test;Cardiopulmonary Exercise Test;Serological test;Echocardiogram; | — |
Secondary
| Measure | Time frame |
|---|---|
| Psychological Assessment and Quality of Life Assessment;Hospitalization details;Compliance Assessment;Adverse Event Risk Assessment; | — |
Countries
China
Contacts
Public ContactLingyu Kong
Tianjin Fourth Central Hospital
Outcome results
None listed