acute heart failure
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. The subject was discharged with acute heart failure as the primary diagnosis; New York Cardiac Function Scale (NYHA) Class II-IV; 2. Aged >=18 years; 3. Subjects are willing to wear wearable devices during the 90-day study; 4. Sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Non-cardiovascular diseases such as dementia and disability can not complete the assessment; 2. Patients who did not want to participate in the research project; 3. Patients with a life expectancy of less than 6 months due to advanced diseases other than HF; 4. Patients with angina pectoris in daily activities or resting state; 5. Patients with embolic events (=70mmHg); 9. Symptomatic or severe aortic stenosis, mitral stenosis, and hypertrophic obstructive cardiomyopathy; 10. Malignant arrhythmias, high atrioventricular block; 11. Known skin allergy to adhesives (hydrocolloid, silica gel, acrylic acid); 12. The visual and tactile ability of the subject or caregiver is unable to use smartphones and household devices.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pulmonary function assessment;Cardiorespiratory endurance;Anxiety and depression;The quality of life;Mortality and readmission rates; | — |
Countries
China
Contacts
West China Hospital of Sichuan University