none
Conditions
Interventions
None listed
Sponsors
The University of Tokyo
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1)Healthy Japanese men and women aged 80 years or older at the time consent is obtained. 2)Persons who have given written consent to participate in this study. 3)People who can wear a wearable device during sleep. 4)Persons who can charge the wearable device themselves or a family member. 5)People who can perform simple operations on the loaned tablet by touching the screen.
Exclusion criteria
Exclusion criteria: 1)People certified as requiring nursing care 2 or above. 2)People with clearly impaired cognitive function. 3)People with a history or current illness that causes cognitive decline. 4)people with clinically significant diseases. 5)People who are participating in clinical research or clinical trials of other medicines or foods. 6)Persons who are judged to be inappropriate as subjects by the principal investigator or research assistant.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Digital information(for 12 months from the start of the study,24 months for those who agree to an extension) Background investigation,quality of life survey,physical function tests and laboratory tests(at the beginning and 12th month,at the end of the study(24th month)for those who agree to an extension) | — |
Countries
Japan
Contacts
Public ContactAkiko Kishi
The University of Tokyo Precision Health Department of Bioengineering,Graduate School of Engineering
Outcome results
None listed