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Behavioral Intervention

Lifestyle Changes for Atrial Fibrillation

N/A

Waitlist Available

Led By Amanda Bonikowske

Research Sponsored by Mayo Clinic

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Paroxysmal or persistent atrial fibrillation.

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 1 year

Awards & highlights

Study Summary

This trial looks at how lifestyle changes and rehab may improve AF symptoms before ablation surgery.

Who is the study for?

This trial is for individuals with occasional or ongoing atrial fibrillation who are scheduled for a catheter ablation procedure. It's not suitable for those who've had this procedure before, have a pacemaker/ICD, suffer from long-term persistent AF, or have uncontrolled AF needing urgent treatment.Check my eligibility

What is being tested?

The study is testing the effects of a comprehensive lifestyle program on symptoms related to Atrial Fibrillation. This includes cardiac rehabilitation and aims to improve patient outcomes prior to undergoing catheter ablation.See study design

What are the potential side effects?

Since this intervention involves lifestyle changes and cardiac rehab rather than medication, side effects may include muscle soreness from exercise and potential stress from dietary adjustments.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Select...

I have irregular heartbeats that come and go or stay.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 1 year

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~1 year

This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Number of Cardiac Rehab Sessions Attended

Secondary outcome measures

Change in Atrial Fibrillation (AF) Symptom severity

Change in exercise capacity

Change in weight loss

+1 more

Trial Design

2Treatment groups

Experimental Treatment

Active Control

Group I: Lifestyle Interventions Pre-ProcedureExperimental Treatment1 Intervention

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.

Group II: Standard of CareActive Control1 Intervention

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.

0 / 1Eligibility criteria met

Find a Location

Who is running the clinical trial?

Mayo ClinicLead Sponsor

3,208 Previous Clinical Trials

3,767,010 Total Patients Enrolled

32 Trials studying Atrial Fibrillation

13,548 Patients Enrolled for Atrial Fibrillation

Amanda BonikowskePrincipal InvestigatorMayo Clinic

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any available vacancies in the trial for participants?

"Taken from clinicaltrials.gov, it appears that this medical investigation has ceased recruitment for the time being: It was posted on January 1st 2024 and most recently updated on December 1st 2023. However, 488 other studies are still open at present."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

A Study of a Lifestyle Program on Recurrent Atrial Fibrillation

Amanda R. Bonikowske 2024. "A Study of a Lifestyle Program on Recurrent Atrial Fibrillation". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT06155357.