COVID-19
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients diagnosed with COVID-19 by positive SARS-CoV-2 PCR test results within 1 week of study enrollment
Exclusion criteria
Exclusion criteria: 1) Unable to wear and use a wearable device 2) Unable to use a smartphone and a smartphone app to connect the wearable device 3) COVID-19 patients with serious condition as ventilator use at registration and unable to obtain informed consent from the patient 4) Others who are deemed unsuitable to include in this study by the principal investigator or sub-investigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Composite of relapse of COVID-19-like symptoms that did not lead to hospitalization, readmission due to COVID-19-like symptoms, oxygen administration, intubation/ventilator use, ECMO use, or all-cause death | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Relapse of COVID-19-like symptoms that did not lead to hospitalization 2) Readmission due to COVID-19-like symptoms 3) Oxygen administration 4) Intubation/ventilator use 5) ECMO use 6) All-cause death | — |
Countries
Japan
Contacts
Kanazawa University Innovative Clinical Research Center (iCREK) / Department of Cardiovascular Medicine