Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06615609

"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 intervention's 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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 6 months

Participants receive health management guidance from a health manager once a week and, if assigned to the experimental group, use the "Smart family doctor" AI-assisted application for personalized disease management. Participants wear a smart band daily to collect health data during the study.

Weekly visits for up to 6 months

Trial Site Locations

Total: 1 location

1

Xinjiang's First Affiliated Hospital of medical university

Ürümqi, Xinjiang, China, 102300

Actively Recruiting

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Research Team

L

Lihua Zhang Zhang, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Design and rationale of the artificial intelligent dialogue System assisted comprehensive Management of secondary prevention Among post coronary aRtery bypass graft patienTs (SMART): protocol for a randomised controlled trial for postcoronary artery bypass grafting management.

Lubi Lei, Jingkuo Li, Lihua Zhang...

https://pubmed.ncbi.nlm.nih.gov/41218945