1. Patients with depressive disorder or bipolar disorder 2. Patients with dementia, mild cognitive impairment, or subjective cognitive impairment 3. Healthy volunteers
Conditions
Interventions
Video/infrared/voice recording during 10 minutes conversation with psychiatrist and/or psychologist. Total number of recording will be 5 times or less. Recording will be done on the doctor visit and t
Sponsors
Keio University School of Medicine
Keio University Science and Technology Omron corporation Advanced Media corporation FRONTEO Healthcare, Inc.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: As patients (1) a) Out/in-patients at Keio university hospital diagnosed as depressive disorder or bipolar disorder b) Out/in-patients at Keio university hospital diagnosed as dementia, mild cognitive impairment, or subjective cognitive impairment (2) 20 years old or older (3) Decisionally not impaired judged by treating physician As healthy volunteers (1) Healthy volunteers who offered participation to the study through web site.
Exclusion criteria
Exclusion criteria: As patients (1) Patients whose illness can be exacerbated by the interview of the study. (2) Patients who have comorbidities that can interfere with the measurements in the study; such as patients with facial palsy or involuntary movement, patients with quadriplegic palsy or involuntary motion, patients with dysphonia by laryngectomized. (3) Those who are considered to be ineligible by the PI or investigators. As healthy volunteers (2) and (3) described above
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To examine the feasibility and safety of data collection according to the current protocol. | — |
Countries
Japan
Contacts
Public ContactMomoko Kitazawa
Keio University School of Medicine Department of Neuropsychiatry
Outcome results
None listed