"Smart Family Doctor" Assisted Comprehensive Management of Secondary Prevention Among Post Coronary Artery Bypass Graft Patients or Post Percutaneous Coronary Intervention Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorChina National Center for Cardiovascular Diseases

About this trial

This study aims to evaluate the effect of an AI-assisted "Smart family doctor" digital health management tool on improving the control rates of hypertension, diabetes, and dyslipidemia in post-CABG (coronary artery bypass grafting) patients or post-PCI (percutaneous coronary intervention) patients. A randomized controlled trial design will be used, involving approximately 5-10 hospitals and 536 participants. Eligible participants are adults aged 18 or older, post-CABG or post-PCI patients with hypertension, diabetes, and dyslipidemia.

Eligibility criteria

Qualifiers

Age ≥ 18 years.

History of CABG surgery or PCI with history of hypertension, diabetes, and dyslipidemia.

Systolic blood pressure no less than 130 mmHg or diastolic blood pressure no less than 80 mmHg

HbA1c no less than 7%

Disqualifiers

History of heart failure or severe arrhythmias.

Presence of other severe underlying conditions such as cancer or liver and kidney insufficiency.

Pregnancy, lactation, or plans for pregnancy within the next year.

Cognitive, communication impairments, or limitations in daily activities.

Trial design

Treatments tested in this trial

  • Smart family doctor
  • Health manager

Treatment groups

536 Participants
are divided into 2 treatment groups

Sponsors and collaborators

China National Center for Cardiovascular Diseases

Lead sponsor

Chinese Academy of Medical Sciences, Fuwai Hospital

Collaborator