Ischemic Heart Disease
Conditions
Interventions
This program is a 14-week program consisting of a 12-week lifestyle intervention and 5-day lifestyle assessments conducted before and after the intervention. The lifestyle assessment is conducted for
Sponsors
Aichi Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients who underwent percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG) for chronic coronary syndrome or acute coronary syndrome 2. Patients who are willing to receive remote lifestyle intervention after hospital discharge 3. Adults aged 20 years or older who are able to understand the study and provide written informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients who show abnormal cardiovascular responses during exercise, including ischemic ST changes, serious arrhythmias, or abnormal blood pressure responses 2. Patients with atrial fibrillation 3. Patients with left ventricular ejection fraction (LVEF) < 40% 4. Patients undergoing hemodialysis 5. Patients who are unable to use a smartphone or tablet device 6. Patients judged by physician to be unsuitable for remote lifestyle intervention 7. Patients who will participate in outpatient cardiac rehabilitation after discharge
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Feasibility of the web-based intervention assessed by the frequency of data entry and the dropout rate 2. Achievement rate of management targets for cardiovascular risk factors (blood pressure, lipid profile, blood glucose, body weight, physical activity, and dietary nutrient intake) | — |
Secondary
| Measure | Time frame |
|---|---|
| Change from baseline in cardiovascular risk factors (blood pressure, lipid profile, blood glucose, body weight, physical activity, and dietary nutrient intake) | — |
Countries
Japan
Contacts
Public ContactKuya Funaki
Aichi Medical University Department of Cardiology
Outcome results
None listed