Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT07270757

Impact of Pre-Ablation Prehabilitation on Clinical Outcomes and Cardiorespiratory Fitness in Atrial Fibrillation Patients

Led by Nanjing Medical University · Updated on 2025-12-08

100

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

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.

CONDITIONS

Official Title

Impact of Pre-Ablation Prehabilitation on Clinical Outcomes and Cardiorespiratory Fitness in Atrial Fibrillation Patients

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 to 70 years
  • Scheduled for first atrial fibrillation ablation
  • New York Heart Association (NYHA) class I or II
  • Left ventricular ejection fraction (LVEF) of 50% or higher
Not Eligible

You will not qualify if you...

  • Significant structural heart disease such as severe valvular disease
  • Contraindications to cardiopulmonary exercise testing or exercise training
  • Cognitive impairment preventing cooperation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The First Affiliated Hospital with Nanjing Medical University

Nanjing, Please Select, China

Actively Recruiting

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Research Team

K

Kexin Wang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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