A Prospective, Multi-center, Randomized Clinical Trial to Evaluate the Detection of Atrial Fibrillation Using Artificial Intelligence-Enhanced Electrocardiography (SmartECG-AFrisk) Compared With Usual Care in Patients With Suspected Atrial Fibrillation: DEEP-AF
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 1,230
- 试验地点
- 1
- 主要终点
- New diagnosis of atrial fibrillation within 6 months. (confirmed by ECG, Holter, or patch ECG)
研究概览
简要总结
"The DEEP-AF study is a prospective, multi-center, randomized clinical trial evaluating the effectiveness of an artificial intelligence-enhanced electrocardiography algorithm (SmartECG-AFrisk) for early detection of atrial fibrillation (AF) in adults with suspected AF but no prior diagnosis. A total of 1,230 participants will be enrolled across 13 centers in Korea and randomized 1:1 into standard care or AI-guided care arms.
In the standard care arm, diagnostic evaluation follows clinical guidelines with symptom-based use of 12-lead ECG, Holter, or patch ECG. In the AI-guided arm, baseline 12-lead ECGs are analyzed using SmartECG-AFrisk to calculate an AF risk score. Participants are classified as high-risk (score ≥50) or low-risk (<50), and monitoring strategies are determined accordingly, enabling targeted ECG monitoring for high-risk individuals.
The primary objective is to compare the 6-month incidence of newly diagnosed AF between the two arms. Secondary endpoints include AF detection differences between risk groups, healthcare resource utilization per AF diagnosis, anticoagulation initiation rates, major clinical events (stroke, embolism, bleeding, mortality), and patient satisfaction.
This study aims to demonstrate whether integrating AI-driven ECG risk stratification into routine care improves AF detection and optimizes healthcare resource use in real-world clinical practice.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 30 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •- Adults ≥30 years old
- •- Symptoms suggestive of atrial fibrillation (palpitations, dizziness, syncope, dyspnea, chest discomfort)
- •- No evidence of AF on baseline 12-lead ECG
- •- No prior history of AF diagnosis
排除标准
- •- Prior diagnosis of atrial fibrillation
- •- Life expectancy ≤ 1 year
研究组 & 干预措施
Usual Care (General Practice)
Symptom-based evaluation by physicians, including 12-lead ECG, Holter monitoring, or patch ECG at least once within 6 months
干预措施: Usual Care (General Practice) (Other)
AI-ECG Guided Care (SmartECG-AFrisk)
Monitoring strategy determined by SmartECG-AFrisk risk score (≥50 = high-risk vs <50 = low-risk).
干预措施: AI-ECG Guided Care (SmartECG-AFrisk) (Device)
结局指标
主要结局
New diagnosis of atrial fibrillation within 6 months. (confirmed by ECG, Holter, or patch ECG)
时间窗: Baseline (randomization) to 6 months after enrollment. Event date is defined as the first ECG/Holter/patch ECG documenting AF during the 6-month follow-up.
次要结局
未报告次要终点
