Can shedding pounds stop atrial fibrillation in its tracks?
NCT ID NCT07816744
First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time
Summary
Researchers in Denmark are testing whether a structured weight loss program can slow the progression of atrial fibrillation in people who are overweight or obese. The trial enrolls 480 adults with symptomatic paroxysmal or early persistent atrial fibrillation and a body mass index of at least 27. Participants are randomly assigned to either a comprehensive weight loss program with behavioral support, meal replacement, and optional GLP-1 medication, or to standard care alone. Everyone receives guideline-based heart care, and researchers track heart rhythm over 14-day monitoring periods for one year.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A structured weight loss program combining behavioral support, meal replacement, and the GLP-1 drug semaglutide
- What this could lead to
- If it works, this could give doctors a clear weight-loss strategy to slow atrial fibrillation and reduce symptoms in people with obesity.
- What could go wrong
- Weight loss is hard to maintain, and the trial may not show that it changes atrial fibrillation. GLP-1 drugs can cause nausea and other side effects, and the follow-up is only one year.
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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 480 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 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: * Symptomatic paroxysmal\* or persistent\*\* AF * Sinus rhythm at inclusion (Visit 1) * BMI ≥27 kg/m2 * Age\>18 years * At least one 12-lead ECG or other single- or multiple-lead ECG device (e.g. Holter monitor-ing or ECG-providing wearables) documented episode during 6 months prior to inclusion \* Paroxysmal AF in this trial is defined as at least 2 episodes, either self-terminating or cardioverted within 7 days, during 6 months prior to in-clusion \*\*Persistent AF in this study is defined as the following: * Duration of an AF episode \>7 days and \< 6 months * Total documented AF history \< 5 years Exclusion criteria: * Atrial flutter as the primary arrhythmia. (Patients with previous or isolated episodes of atrial flutter may be included, provided that AF is the dominant arrhythmia and the primary target of clinical management) * Implanted electronic device (pacemaker/ICD/ICM) * Type 1 diabetes or Type 2 diabetes on insulin treatment * Severe heart failure (LVEF \<40%) * Inability to sign informed consent * Severe kidney disease (eGFR\<30) * History of catheter ablation for AF * Scheduled to receive catheter ablation for AF during the study period (next 1 year) * Incretin-based therapy (GLP-1 receptor agonists or DPP-IV inhibitors) within 30 days prior to randomization (visit 1) * Scheduled for bariatric surgery during the study period * Hypertrophic cardiomyopathy, ARVC/D, non-compaction or amyloidosis * Chronic or previous acute pancreatitis * Current participation in any other clinical intervention trial that may result in changes to med-ical management during the study period * Women of childbearing potential who are not on an acceptable form of contraception * Pregnant or breastfeeding women * Personal or family history of medullary thyroid carcinoma (MTC) * History of MEN2 (Multiple Endocrine Neoplasia type 2)
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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 places running it
2 sites. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Esbjerg Hospital - University Hospital of Southern Denmark
Esbjerg, 6700, Denmark
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University Hospital Bispebjerg and Frederiksberg
Copenhagen, Denmark
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