A Study of a Lifestyle Program on Recurrent Atrial Fibrillation

Mayo Clinic

Status: Withdrawn

Conditions: Atrial Fibrillation

Treatments: Behavioral: Multicomponent lifestyle intervention program

Study type: Interventional

Funder types: Other

Identifiers

NCT06155357

23-003042

Details and patient eligibility

About

The purpose of this study is to examine the impact of a comprehensive lifestyle intervention, including cardiac rehabilitation, prior to catheter ablation (a procedure to stop abnormal electrical signals in the heart), on Atrial Fibrillation (AF)-related symptoms.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Paroxysmal or persistent atrial fibrillation.
• Planned elective catheter ablation of AF.

Exclusion criteria

• Prior catheter ablation.
• Presence of pacemaker/ICD.
• Longstanding persistent AF.
• Uncontrolled AF (including poor rate control or tachycardia-mediated cardiomyopathy requiring urgent cardioversion/ablation at the clinician's assessment).

Trial design

Primary purpose: Health Services Research

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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0 participants in 2 patient groups

Lifestyle Interventions Pre-Procedure

Experimental group

Description:

Subjects with paroxysmal or persistent atrial fibrillation (AF) who are scheduled to undergo elective catheter ablation of AF will participate in a 12-week multicomponent lifestyle intervention program.

Treatment:

Behavioral: Multicomponent lifestyle intervention program

Standard of Care

No Intervention group

Description:

Subjects who have previously undergone catheter ablation of atrial fibrillation (AF) as part of their standard of care will have medical chart review completed to gather information.