None listed
Conditions
Interventions
Medical Device : Application time: 60 minutes each test
Application period: 3 weeks in total (2nd evaluation, 3rd evaluation at intervals of 1 week after the 1st evaluation)
Sponsors
Jeonbuk National University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Adult men and women between the ages of 18 and 85 2) Those with a K-MMSE score of 26 or less showing cognitive decline 3) A person who can read and understand the subject's explanation and consent form, voluntarily decides to participate and gives written consent to the subject's consent form and is able to respond to the questionnaire
Exclusion criteria
Exclusion criteria: 1) Patients with acute brain disease (e.g., stroke, traumatic brain injury within 6 months) 2) Those with acute medical conditions 3) Those who are judged inappropriate to participate in this clinical trial according to the judgment of other researchers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| intraclass Correlation Coefficient of neurocognitive function items (attention test, memory test, sensory and motor test, coordination test, problem-solving ability test) | — |
Secondary
| Measure | Time frame |
|---|---|
| intraclass Correlation Coefficient of neurocognitive function items (attention test, memory test, sensory and motor test, coordination test, problem-solving ability test) | — |
Countries
Korea, Republic of
Contacts
Public ContactSeung-Rok Kang
Jeonbuk National University Hospital
Outcome results
None listed