No booze, better beat: study tests alcohol abstinence after AF ablation
NCT ID NCT07528729
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether staying alcohol-free for six months after a heart ablation procedure can reduce the return of atrial fibrillation (AF), a common heart rhythm problem. Researchers will enroll 414 adults who drink at least three alcoholic beverages per week and are scheduled for their first AF ablation. Participants will either receive nurse-led support to quit alcohol or continue their usual habits. The study uses a smartwatch to track heart rhythms and will also measure symptoms, quality of life, and long-term outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- alcohol abstinence (behavioral intervention)
- What this could lead to
- If successful, this could show that stopping alcohol for six months after ablation reduces the chance of atrial fibrillation returning, offering a simple lifestyle change to improve outcomes.
- What could go wrong
- This is a behavioral study with no blinding, so results may be influenced by participant awareness. The intervention requires significant commitment, and long-term benefits beyond six months are not yet known.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 414 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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May 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * All patients \>18 years old * Referred to a first-time AF or AFL ablation * Scores ≥3 on AUDIT/ ≥3 drinks per week * Can use the ScanWatch2 as described Exclusion Criteria: * Patients who do not have a Danish social security number * Patients who cannot read, and speak Danish fluently * Unable to give informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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