Left ventricular assist device
Conditions
Interventions
Wear a wearable device for 90 days to manage physical activity while providing disease management, exercise and nutritional guidance
Sponsors
Kyushu University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Discharged from the hospital for more than 3 months 2. Agreement 3. Age 20 years and older
Exclusion criteria
Exclusion criteria: 1. Patients with difficulty measuring exercise tolerance due to musculoskeletal disease 2. Patients with re-hospitalization for acute exacerbation of heart failure within 1 month 3. Patients who do not have their own smartphone 4. Patients who are determined by the study investigator, study sponsor, or attending physician to be inappropriate as study subjects
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in the Peak VO2 | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in AT, Peak watt and VE/VCO2 slope Change in KCCQ Change in number of steps, physical activity and 5m walk speed Change in muscle (grip strength, knee extension muscle strength and respiratory muscle strength) Change in anxiety and depression Change in FAI | — |
Countries
Japan
Contacts
Public ContactTomoyuki Nezu
Kyushu University Hospital Department of Rehabilitation Medicine
Outcome results
None listed