none
Conditions
Interventions
None listed
Sponsors
The University of Tokyo
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Men and women who are 80 years old or older at the time of obtaining consent 2) Those who have obtained written consent to participate in this study 3) Persons who have obtained written consent in a separate document regarding the implementation of genetic testing 4) Those who can wear a wearable device while sleeping 5) Those who can charge the wearable device by themselves or their family 6) Those who can perform simple operations by touching the screen on a loaned tablet
Exclusion criteria
Exclusion criteria: 1) Persons who have been certified as requiring long-term care 2) Persons with apparently impaired cognitive function 3) Persons with a medical history or current medical history that causes cognitive decline 4) Persons with clinically significant illness 5) Those who have participated in clinical research and clinical trials of other drugs and foods within the past month 6) Persons judged by the principal investigator or coordinator to be inappropriate as subjects
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Acquisition rate of digital data and sample collection data from super-elderly people | — |
Secondary
| Measure | Time frame |
|---|---|
| Confirmation of distribution of biomarkers that are considered to be targets Selection of indicators related to lifestyle evaluation Registration rate by age group for the number of consents obtained | — |
Countries
Japan
Contacts
Public ContactAkiko Kishi
The University of Tokyo Precision Health Department of Bioengineering,Graduate School of Engineering
Outcome results
None listed