Key result
AI-ECG-guided Holter screening tests early detection of atrial fibrillation vs usual care.
Why the study?
Traditional risk scores provide limited value for predicting short-term latent AF and the clinical utility of AI-ECG algorithms remains unvalidated in randomized controlled trials.
Does AI-ECG-guided risk stratification combined with targeted ambulatory Holter monitoring improve the early detection of newly diagnosed AF or pre-AF atrial findings in patients undergoing routine ECGs?
RCT (n=14,726)
Open-label
1:1
No
Does AI-ECG-guided risk stratification combined with targeted ambulatory Holter monitoring improve the early detection of newly diagnosed AF or pre-AF atrial findings in patients undergoing routine ECGs?
The LATENT trial will provide randomized evidence on whether an AI-ECG-guided screening strategy increases the early detection of atrial fibrillation and high-risk atrial arrhythmias compared to usual care.
First RCT of AI-ECG-guided Holter monitoring for latent AF; extends observational algorithms to randomized evidence for targeted screening.
Background: Atrial fibrillation (AF) is a progressive condition that is often undiagnosed until adverse events occur. Traditional risk scores provide limited value for predicting short-term latent AF. Artificial intelligence (AI)-enabled electrocardiogram (ECG) algorithms enable early risk stratification from sinus rhythm ECGs, however their clinical utility remains unvalidated in randomized controlled trials (RCTs). Objective: To evaluate an AI-ECG-guided strategy for targeted ambulatory Holter monitoring to enhance the early detection of AF or pre-AF atrial findings (PAAFs, defined as premature atrial complexes [PACs] > 500 beats per 24 hours, consecutive short runs of PACs > 20 beats, or non-sustained AF or atrial flutter) compared with usual care. Design: The LATENT trial is a prospective, open-label, two-arm RCT (NCT06847932) that will recruit 14,726 participants undergoing routine ECGs at a tertiary medical center in Taiwan. Participants will be randomized 1:1 to the intervention group (AI-ECG risk stratification) or control group (usual care). In the intervention group, high-risk individuals identified by the AI-ECG model will be invited to undergo up to 7 days of ambulatory Holter monitoring. In the control group, AI-ECG analysis will be retrospectively applied after study completion to identify those at high risk. The primary endpoint is newly detected AF or PAAFs within 90 days. Summary: This trial will evaluate the clinical utility of an AI-ECG-guided risk stratification strategy combined with targeted ambulatory Holter monitoring for the early detection of AF or PAAFs in a real-world hospital setting. The findings will inform future strategies for integrating AI-ECG technology to support early AF detection and prevention.
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Lee et al. (2026) conducted an RCT in Atrial fibrillation (n=14,726). AI-ECG-guided strategy for targeted ambulatory Holter monitoring vs. Usual care was evaluated on Newly detected AF or pre-AF atrial findings (PAAFs) within 90 days. An AI-ECG-guided strategy for targeted ambulatory Holter monitoring will be evaluated against usual care in 14,726 participants to assess early detection of atrial fibrillation or PAAFs within 90 days.
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