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Atrial Fibrillation (AF)PACE-AFNCT07726056

Performance After Cardiac Ablation in Endurance Athletes for Atrial Fibrillation

A study testing Ablation in people with Atrial Fibrillation (AF), run by University Hospital of Leuven Leuven at 5 sites in 2 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The relationship between exercise and atrial fibrillation (AF) seems to follow a J-shaped curve: while moderate activity reduces AF risk, both insufficient and excessive endurance exercise increase susceptibility. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Atrial Fibrillation (AF)
What is being tested?
Ablation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
5 sitesin 2 countries
Study dates
1 Mar 2026to 31 Dec 2032
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18-80 years
  • Participation in endurance sports (≥4 hours/week)
  • Diagnosis of atrial fibrillation
  • Capturing training data through commercially available platforms (e.g. Strava, TrainingPeaks, …) or willingness to start collecting training data and working with these commercially available platforms prospectively

Who cannot join

  • No training data available
  • History of cardiovascular disease (including ischemic heart disease, cardiomyopathy, valvular heart disease, primary electrical disorders, or congestive heart failure)
  • Active smoking

Trial locations and contacts

5 sites in 2 countries. Contact the study team or a site near you to ask about taking part.

Boris Delpire, MD contact

+32477399875

boris.delpire@uhasselt.be

Guido Claessen, MD, PhD contact

claessen.guido@gmail.com

5 sites in 2 countries

Belgium4 sites, 4 recruiting
  • Universitair Ziekenhuis Antwerpen

    Antwerp, Antwerpen, 2000

    Hein Heidbuchel, MD, PhD, +32 3 821 30 00, Anke.DeSchutter@uza.be

    Recruiting
  • ZOL Genk

    Genk, Limburg, 3600

    Laurent Pison, MD, PhD, +32 89 32 50 50, michiel.dewever@zol.be

    Recruiting
  • Jessa Hospital, Department of Cardiology

    Hasselt, Limburg, 3500

    Boris Delpire, MD, +32477399875, boris.delpire@uhasselt.be

    Recruiting
  • UZ Leuven

    Leuven, Vlaams-Brabant, 3000

    Rik Willems, MD, PhD, +32 16 33 22 11, sofie.vansoest@uzleuven.be

    Recruiting

Other trials in Belgium

Australia1 site, 1 recruiting
  • St. Vincent's Hospital

    Melbourne

    Andre La Gerche, MD, PhD, +61 3 9231 2211, kristel.janssens@svi.edu.au

    Recruiting

Other trials in Australia

About this study

The relationship between exercise and atrial fibrillation (AF) seems to follow a J-shaped curve: while moderate activity reduces AF risk, both insufficient and excessive endurance exercise increase susceptibility. In athletes, standard treatments such as antiarrhythmic drugs often provide only partial symptom control and may impair performance through fatigue, chronotropic incompetence and side effects. Pulmonary vein isolation (PVI) may offer a more definitive therapeutic option but carries risks of atrial fibrosis, stiffening, and altered autonomic regulation, which may also influence exercise capacity. The investigators hypothesize that ablation will have a significant impact-either beneficial or detrimental-on the physical performance of athletes with AF. However, existing evidence is limited to small studies with inconsistent findings, underscoring the need for a dedicated study.

This prospective, multicentre interventional study will assess the effects of cardiac ablation in 100 endurance athletes with AF. Participants will undergo comprehensive pre- and post-ablation phenotyping, including electrocardiogram (ECG), cardiopulmonary exercise testing (CPET), echocardiography, Holter monitoring, and detailed training data collection (efficiency factor, acute and chronic training load). Clinical follow-up will extend to 12 months post-ablation.

Read more

The primary endpoint is the change in peak VO₂ (mL/kg/min) measured before ablation and after the procedure.

Secondary analyses will explore:

  • Autonomic adaptations: including changes in maximum heart rate, heart rate recovery, heart rate reserve, and heart rate variability.
  • Cardiac function: alterations in diastolic and atrial function assessed by echocardiography.
  • Training and performance: objective measures such as efficiency factor, decoupling, functional threshold power, critical power, and acute and chronic training load.
  • Technique comparison: differences in outcomes between pulsed field and radiofrequency ablation (e.g. atrial function, troponin release, …).
  • Sex-specific effects: recognising the underrepresentation of women in sports cardiology research, the investigators will include female athletes according to incidence and evaluate potential differences in treatment response between sexes.
  • Predictors of AF recurrence in endurance athletes
Read the detailed description

activity appears protective, both insufficient and excessive exercise are linked to an elevated risk in developing AF. Standard treatments, such as medication or catheter ablation via pulmonary vein isolation (PVI), are widely used in the general population, but their application in athletes presents distinct challenges. Beyond managing the arrhythmia itself, athletes are often concerned about how treatment might impact their performance, return-to-play timelines, and long-term athletic performance. Antiarrhythmic medications are typically only partially effective in this population, rarely resulting in full symptom resolution and frequently causing side effects that undermine athletic performance. The most common issues (fatigue, decreased energy, and impaired physical performance) with antiarrhythmic medications are especially troubling for individuals whose identity and daily life revolve around maximising physical capability.

Cardiac ablation has therefore emerged as a more definitive treatment strategy, with fewer side effects. However, this procedure is not without risks. Understanding the physiological trade-offs of ablation is essential, especially for those whose pursuit of peak performance defines their lifestyle. Cardiac ablation may affect exercise capacity through several mechanisms. Ablation lines render sections of the atrium electrically and mechanically inert, potentially reducing its contractile contribution. Repeat procedures may further increase atrial stiffness. Additionally, targeting autonomic structures such as the ganglionated plexi or ligament of Marshall during ablation can disrupt normal heart rate regulation, potentially diminishing responsiveness during exercise. Conversely, effective symptom control through cardiac ablation may allow athletes to train more consistently and at higher intensities. Reducing AF burden may also slow the progression of atrial remodelling and associated tissue stiffening.

For athletes, whose primary goal is to optimise physical performance, the effects of AF treatment on their ability to train and compete are understandably a major concern. Conversely, eliminating AF symptoms could enhance training consistency and prevent or halt the development of structural remodelling that contributes to disease progression. This duality makes the relationship between ablation and athletic performance a compelling but underexplored topic, not only for athletes, but for all physically active individuals.

Available evidence on the relationship between ablation and athletic performance remains limited. Several small-scale studies have shown that the effectiveness PVI in athletes is comparable to that observed in the general population. A small study by Mandsager et al. found no significant change in exercise capacity before and after PVI among athletes. However, the study's limitations (including a low follow-up rate, delayed post-procedure testing, and a small subset with paired assessments) temper confidence in these findings. While the results provide some reassurance, they highlight the need for larger, prospective studies with standardised protocols. More robust data have been observed on markers of the autonomous system, such as heart rate. Post-PVI, resting heart rate increased by approximately 10 beats per minute and remained elevated for at least 12 months. This was associated with reductions in both heart rate reserve and heart rate recovery, two indicators commonly linked to diminished cardiovascular fitness.

One proposed contributor to the increased incidence of AF in athletes is the chronic hemodynamic load associated with intense endurance training, which may lead to atrial enlargement, inflammation, and eventual fibrosis. Atrial dilation is a recognised component of the athlete's heart, yet findings across studies have been inconsistent. Surprisingly, the research by Mandsager et al. reported no significant differences in cardiac remodelling between athletes and nonathletes, with athletes even demonstrating slightly smaller left atrial volumes. This contrasts with other investigations, including a study by Trivedi et al., which showed that elite endurance athletes had atria more than twice the size of those in healthy controls and marginally larger than individuals with paroxysmal AF.

Earlier intervention with PVI was shown to be linked to better procedural outcomes. This raises the possibility that ablation might be more effective when performed before substantial atrial remodelling occurs. However, many elite athletes already exhibit marked atrial dilation by the time AF presents, making it unclear whether PVI yields comparable success in this subgroup. Although current evidence does not suggest that PVI meaningfully impairs exercise capacity, it also makes clear that the procedure induces lasting changes in cardiac physiology. These changes warrant closer scrutiny, particularly in athletic populations.

With the growing number of athletes diagnosed with AF, it is increasingly important to understand how ablation affects athletic performance. This multicentre project aims to address that gap by systematically assessing the impact of cardiac ablation using objective performance metrics, advanced cardiac imaging, and athlete-reported outcomes. The primary goal of this project is to provide a scientific basis for the clinical decision-making in athletes with AF. Through a better understanding of the effects of cardiac ablation on AF, this project may lead to improved and more informed therapeutic strategies in athletes with AF.

Primary Hypothesis: Catheter ablation for AF in endurance athletes results in measurable changes in athletic performance, either beneficial or detrimental, due to shifts in cardiac physiology and autonomic function.

Primary objective:

The primary endpoint is the change in peak VO₂ (mL/kg/min) between baseline (before ablation) and follow-up.

Secondary objectives:

  • Autonomic adaptations: including changes in maximum heart rate, heart rate recovery, heart rate reserve, and heart rate variability.
  • Cardiac function: alterations in diastolic and atrial function assessed by echocardiography.
  • Training and performance: objective measures such as efficiency factor, decoupling or cardiac drift, functional threshold power, critical power, and acute and chronic training load.
  • Technique comparison: differences in outcomes between pulsed field and radiofrequency ablation (e.g. atrial function, troponin release, …).
  • Sex-specific effects: recognising the underrepresentation of women in sports cardiology research, the investigators will include female athletes according to incidence and evaluate potential differences in treatment response between sexes.
  • Predictors of AF recurrence in endurance athletes
Being tested
Ablation
Keywords
Athletes, Sports Cardiology, Atrial Fibrillation, Ablation, Endurance, Performance
Medical subject headings
Atrial Fibrillation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AblationOther

    The ablation procedure will be limited to pulmonary vein isolation (PVI) alone, without additional extensive ablation such as posterior wall, isthmus, or linear lesions on the left or right atrium. If atrial flutter is documented in the patient's medical history, or if it is strongly suspected or inducible during the electrophysiology study, a cavotricuspid isthmus (CTI) ablation will be performed. The choice of energy modality (e.g., pulsed field ablation, cryoablation, or radiofrequency ablation) will be at the discretion of the electrophysiologist, according to procedural goals and institutional standards. When deemed appropriate by the treating physician, an assessment of the underlying arrhythmogenic substrate using electroanatomical mapping may be undertaken; however, this is not mandatory. Similarly, if available and preferred by the participating centre, intra-atrial pressures may be recorded, though this is also optional. Following the ablation, a one-month blanking period wil

Study groups in NCT07726056
Study groupRoleWhat they receive
Endurance athletesOtherNot described
Receives: Other: Ablation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in peak VO2

    The primary endpoint is the change in peak VO₂ (mL/kg/min) between baseline (before ablation) and follow-up.

    Measured: From enrollment to 8 weeks post-ablation.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jul 2026
  2. Study start1 Mar 2026
  3. Primary completion31 Dec 2030 (estimated)
  4. Study completion31 Dec 2032 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07726056
Sponsor's protocol ID
3113
Acronym
PACE-AF
Status last verified
Jul 2026
First submitted
21 Jul 2026
Last updated
27 Jul 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Ablation in people with Atrial Fibrillation (AF), run by University Hospital of Leuven Leuven at 5 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 27 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 5 sites in Belgium, Australia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Boris Delpire, MD (+32477399875, boris.delpire@uhasselt.be), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in peak VO2 (time frame: From enrollment to 8 weeks post-ablation.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Jul 2026.

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