AI-guided exercise and recovery program for people with coronary heart disease
Artificial Intelligence-enhanced Stratified Management Platform Guiding Home-based Exercise Rehabilitation for Coronary Heart Disease Patients: a Randomized Control Trial
NA · China National Center for Cardiovascular Diseases · NCT07259278
This project will see if a smartphone AI program combined with a wristband helps adults with coronary heart disease do home exercise after leaving the hospital and improves their fitness and heart-risk measures.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | China National Center for Cardiovascular Diseases (other gov) |
| Locations | 1 site (Beijing, Beijing Municipality) |
| Trial ID | NCT07259278 on ClinicalTrials.gov |
What this trial studies
Adults with coronary heart disease who are classified as low exercise risk will be assigned to either an AI-enabled stratified management platform used with a sports wristband or to routine post-discharge care and followed for three months. The AI platform provides personalized exercise prescriptions, remote monitoring via the wristband, motivational support, and tailored risk-factor management through a smartphone app. The primary outcome is change in peak oxygen consumption (VO2peak) at 3 months, with secondary outcomes including daily physical activity, exercise adherence and motivation, control of modifiable cardiovascular risk factors, and safety of home-based exercise. Baseline and follow-up visits occur at Fuwai Hospital with ongoing remote data collection through the app and wearable.
Who should consider this trial
Good fit: Adults over 18 with coronary heart disease who are judged low-risk for exercise by the GRACE score, can use a smartphone (or have a caregiver who can), and are willing to provide informed consent are ideal candidates.
Not a fit: Patients with recent myocardial infarction, planned revascularization, significant left main or major vessel stenosis, severe cognitive or exercise impairment, advanced malignancy, multi-organ failure, or life expectancy under three months are unlikely to benefit or to be eligible.
Why it matters
Potential benefit: If successful, the platform could help patients increase exercise capacity, improve adherence to home rehabilitation, and better control cardiovascular risk factors.
How similar studies have performed: Previous telerehabilitation and digital cardiac rehabilitation programs have improved adherence and exercise capacity, but AI-driven stratified management platforms are relatively novel and less extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * CHD patients aged over 18 years; * Stratified as low-risk for cardiovascular events during exercise and classified as low-risk according to the GRACE risk score. * Ability of the patient or close relatives to use smartphones and applications; * Willingness to participate and sign the informed consent form. Exclusion Criteria: * Residual stenosis of \>50% in the left main coronary artery, or \>70% stenosis in other major epicardial vessels; * Planned coronary revascularization within the next 3 months; * Acute myocardial infarction within the past 1 month; * Severe cognitive impairment; * Severely impaired exercise capacity. * Advanced-stage malignancy; * Life expectancy less than 3 months; * Severe multi-organ failure; * Other conditions deemed unsuitable for home-based exercise rehabilitation following assessment by a specialist rehabilitation physician. * Refusal to provide written informed consent.
Where this trial is running
Beijing, Beijing Municipality
- Fuwai Hospital, Chinese Academy of Medical Sciences/National Center for Cardiovascular Diseases — Beijing, Beijing Municipality, China (RECRUITING)
Study contacts
- Study coordinator: Prof. Gao, MD, PhD
- Email: sophie_gao@sina.com
- Phone: 010-88322413
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Secondary Prevention of Coronary Heart Disease