Impact of Pre-Ablation Prehabilitation on Clinical Outcomes and Cardiorespiratory Fitness in Atrial Fibrillation Patients
Recruiting · NCT07270757 · Interventional (participants receive a specific treatment) · Lead sponsor: Nanjing Medical University
View the official record on ClinicalTrials.gov →Interventions studied
4-week structured prehabilitation program (exercise training + psychological education)
What this trial is about
The primary objective of this study is to compare the effects of a preoperative prehabilitation program versus usual care on post-procedural cardiorespiratory function and clinical outcomes in patients undergoing catheter ablation for atrial fibrillation.
Who can take part
Age range
18 Years to 70 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Aged 18-70 years
- Scheduled for first AF ablation
- NYHA class I-II
- LVEF ≥ 50%
Exclusion criteria
- Significant structural heart disease (e.g., severe valvular disease)
- Contraindications to CPET or exercise training
- Cognitive impairment preventing cooperation
Where it is running
1 location listed.
- The First Affiliated Hospital with Nanjing Medical University - Nanjing, Please Select, China