none
Conditions
Interventions
None listed
Sponsors
TOKYO CENTER CLINIC
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Who have fully understood the purpose and content of this study and have given written consent 2. Male and Female 18 years of age or older
Exclusion criteria
Exclusion criteria: 1. Those with evidence of chronic arrhythmia. 2. Who have uneven skin or dark skin such as black spots on the wrists due to wounds, burns, etc. 3. Who have a limb defect or a shunt in the left upper limb. 4. Who have difficulty in wearing the wearable device used in this evaluation test. (Minimum forearm circumference is less than 130 mm or more than 195 mm) 5. at Rest (1) Those whose upper arm does not fit the cuff size for aneroid sphygmomanometer. (Those whose upper arm circumference is 200 mm or less or whose upper arm circumference is 420 mm or more) 6. in Motion (1) Those whose upper arm does not conform to the cuff size for ABPM. (Those whose upper arm circumference is less than 200mm or more than 420mm.) (2)Those who cannot perform walking movements using a treadmill at a speed of 1.5 km to 3 km per hour.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Deviation between blood pressure measured by aneroid sphygmomanometer and the device under study. Deviation between ABPM and blood pressure measured by the device under study. | — |
Countries
Japan
Contacts
Public ContactKeiko Watabe
TOKYO CENTER CLINIC Clinical Research Group
Outcome results
None listed