NCT lookup

Pull any trial record directly from ClinicalTrials.gov.

Effectiveness of an AI-Enabled Stratified Management System for Premature Coronary Artery Disease
Effectiveness of an AI-Enabled Stratified Management System for Premature Coronary Artery Disease

NCT07031531

RecruitingNA

Sponsor: China National Center for Cardiovascular Diseases

Conditions: Premature Coronary Heart Disease

Interventions: AI-Enabled Stratified Management System, Usual Post-Discharge Care

Countries: China

The goal of this clinical trial is to learn if an AI-enabled stratified management system (SMART-CHD) can improve post-discharge outcomes in adults aged 18-45 with premature coronary artery disease. The main questions it aims to answer are: 1. Does SMART-CHD reduce the combined rate of all-cause death, myocardial infarction, stroke and rehospitalization within 12 months? 2. Does SMART-CHD achieve better control of modifiable risk factors compared with usual care? Researchers will compare SMART-CHD to standard discharge management (verbal and printed instructions on medications, follow-up timelines and lifestyle advice) to see if the AI-driven platform leads to fewer adverse events and improved risk-factor profiles. Participants will: 1. Install and use the SMART-CHD mobile app after a 10-minute structured orientation session with supervised simulations. 2. Complete regular in-app surveys on lifestyle behaviors, laboratory/imaging results and clinical events (with OCR-powered LLM assistance). 3. Wear paired sensors for continuous monitoring of blood pressure, heart rate and other physiologic metrics. 4. Receive automated EHR data harvesting, AI-driven voice-call reminders, and real-time CRC support via a dedicated WeChat group. 5. Follow personalized, guideline-based risk-factor recommendations (diet, exercise, sleep, weight, smoking, alcohol, hypertension, dyslipidemia, diabetes).

Eligibility overview

Sex: ALL

Age: 18 Years to 45 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria

1. Patients with coronary heart disease aged 18-45 years;
2. The patient or a close family member is capable of using a smartphone and mobile application (App);
3. Willing to participate in the study and able to provide written informed consent.

Exclusion Criteria

1. Severe cognitive impairment;
2. Advanced-stage malignancy;
3. Life expectancy less than 12 months;
4. Severe multi-organ failure;
5. Refusal to provide written informed consent.
Locations (16)
  • Hefei, Anhui, China
  • Beijing, Beijing Municipality, China
  • Shenzhen, Guangdong, China
  • Shijiazhuang, Hebei, China
  • Shijiazhuang, Hebei, China
  • Luoyang, Henan, China
  • Zhengzhou, Henan, China
  • Zhengzhou, Henan, China
  • Zhengzhou, Henan, China
  • Nanjing, Jiangsu, China
  • Yangzhou, Jiangsu, China
  • Xi'an, Shaanxi, China
  • Xi'an, Shaanxi, China
  • Taiyuan, Shanxi, China
  • Luzhou, Sichuan, China
  • Hangzhou, Zhejiang, China