dementia
Conditions
Interventions
Face-to-face consultation period
online medical treatment combination period
Sponsors
Keio University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who visit our memory clinic. Patients with dementia or mild cognitive impairment between the ages of 50 and under 95. Person who can determine that necessary inspection can be performed on the specified date after obtaining consent Study partners have at least 7 hours of contact with the subject per week and can accompany all consultations during the observation period. Person who obtained consent in writing from the research participant and study partner Person who can use online medical care.
Exclusion criteria
Exclusion criteria: Person with a history of substance use disorder other than smoking or being treated Person who has a history of epilepsy or is being treated Persons receiving antidepressants, antipsychotics, hypnotics including long-term sleeping pills Persons with a history of psychiatric/neurological disorders that affect cognitive function Persons with serious complications
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main endpoints in this study are measured at the start of the study (0 weeks), 24 weeks, and 48 weeks by the three-time evaluation Zarit care burden scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Cognitive function(MMSE), clinical dementia rating(CDR), questionnaire version Neuropsychiatric Inventory-Brief Questionnaire Form (NPI-Q), Geriatric depression scale 15 (GDS15) at the start of the study (0weeks), 24 weeks, 48weeks 3evaluations. | — |
Countries
Japan
Contacts
Public ContactDaisuke Ito
Keio University School of Medicine Department of Neurology
Outcome results
None listed