ArticleActa Cardiologica Sinica2026
Leveraging AI-ECG Technology for Early Notification and Tracking of AF Development (LATENT): Study Rationale and Design of a Randomized Controlled Trial.
Article in Acta Cardiologica Sinica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06847932 (Leveraging AI-ECG Technology for Early Notification and Tracking of AF Development), which is not on this map. Not yet cited in PubMed.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Leveraging AI-ECG Technology for Early Notification and Tracking of AF Development: a Randomized Control Trial
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15 authors.
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Abstract
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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