Actively Recruiting
Smart Family Doctor Assisted Comprehensive Management of Secondary Prevention Among Post Coronary Artery Bypass Graft Patients or Post Percutaneous Coronary Intervention Patients
Led by China National Center for Cardiovascular Diseases · Updated on 2025-12-08
536
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
Sponsors
C
China National Center for Cardiovascular Diseases
Lead Sponsor
C
Chinese Academy of Medical Sciences, Fuwai Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating an AI-assisted digital health tool called the Smart family doctor to improve control of hypertension, diabetes, and dyslipidemia in adults who have undergone coronary artery bypass grafting CABG or percutaneous coronary intervention PCI. This study uses a randomized controlled design involving about 536 participants across 5-10 hospitals. Participants must be adults aged 18 or older with a history of CABG or PCI and the specified conditions. Participants in the experimental group will use the AI-assisted Smart family doctor app that provides personalized health education, targeted guidance on managing blood pressure, blood sugar, medication adherence, exercise, and smoking cessation. They will also receive tailored reminders and can report self-measured health data for feedback. Both groups receive weekly 3-hour health management guidance from health managers, and participants will wear a smart band daily for health data collection during the 6-month study period. Throughout the study, participants will be assessed for control rates of hypertension, diabetes, and hyperlipidemia at 6 months. Additional measures include blood pressure, cholesterol levels, blood glucose, physical activity, quality of life, psychological status, and cognitive function. The study monitors health data continuously via smart bands and collects self-reports and clinical assessments to evaluate the interventions impact over the 6 months.
CONDITIONS
Brief Title
"Smart Family Doctor" Assisted Comprehensive Management of Secondary Prevention Among Post Coronary Artery Bypass Graft Patients or Post Percutaneous Coronary Intervention Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- History of coronary artery bypass grafting (CABG) surgery or percutaneous coronary intervention (PCI) with hypertension, diabetes, and dyslipidemia
- At least one of the following: systolic blood pressure of 130 mmHg or higher, or diastolic blood pressure of 80 mmHg or higher
- HbA1c level of 7% or higher
- LDL-C level of 1.4 mmol/L or higher
- Use of a smartphone
- Signed informed consent
You will not qualify if you...
- History of heart failure or severe irregular heart rhythms
- Presence of severe conditions such as cancer or liver and kidney failure
- Pregnancy, breastfeeding, or plans to become pregnant within the next year
- Cognitive or communication difficulties, or limitations in daily activities
Research Team
L
Lihua Zhang Zhang, PhD
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here