Patients who, for any reason, measure any vital data with a pulse oximeter, blood pressure monitor, heart rate monitor, respiratory rate monitor, thermometer, or bladder thermometer.
Conditions
Interventions
None listed
Sponsors
Hiroshima University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients undergoing measurement of any vital data including pulse oximetry, blood pressure, heart rate monitoring, respiration rate monitoring, body temperature, and bladder temperature using pulse oximeters, blood pressure monitors, heart rate monitors, respiration rate monitors, thermometers, and bladder thermometers for various reasons at medical facilities such as Fujii Cardiovascular Internal Medicine and Prefectural Hiroshima Hospital. Patients who have received explanations and have provided their informed consent.
Exclusion criteria
Exclusion criteria: Patients for whom obtaining consent through written explanation is challenging. Patients with unstable conditions. Patients deemed inappropriate by their attending physician.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare age, gender, and vital data collected by a wristwatch wearable IoT device with transcutaneous arterial blood oxygen saturation, blood pressure, heart rate, respiratory rate, skin temperature, and bladder temperature measured by a medical device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Training AI with Information from Transcutaneous Arterial Oxygen Saturation, Blood Pressure, Heart Rate, Respiration Rate, Skin Temperature, and Bladder Temperature Measurements in Medical Devices | — |
Countries
Japan
Contacts
Public ContactTatsuya Maruhashi
Research Institute for Radiation Biology and Medicine, Hiroshima University Department of Regenerative Medicine
Outcome results
None listed