1. Patients with major depressive disorder, bipolar I/II disorder, schizophrenia, anxiety disorders, and major/mild neurocognitive disorder by DSM-5 2. Healthy volunteers
Conditions
Interventions
None listed
Sponsors
Keio University School of Medicine
Shizuoka University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Inclusion criteria: As patients (1) Out/in-patients at the study site diagnosed as Major Depressive Disorder, Bipolar I/II Disorder, Schizophrenia, Anxiety Disorders, Major/Mild Neurocognitive Disorder, according to DSM-5. (2) 20 years old or older. (3) Decisionally not impaired judged by treating physician. If judged as decisionally impaired, patients' guardians should give consent. As healthy volunteers (1) Healthy volunteers who offered to participate to the study through web site. (2) 20 years old or older.
Exclusion criteria
Exclusion criteria: Exclusion Criteria: As patients (1) Patients whose illness can exacerbate by interview of the study. (2) Patients who have comorbidities that can interfere with measurements in the study; such as patients with dysphonia by laryngectomy. (3) Those who are considered to be ineligible by the PI or investigators. As healthy volunteers (1) Those who have comorbidities that can interfere with measurements in the study; such as patients with dysphonia by laryngectomy. (2) Those who are considered to be ineligible by the PI or investigators.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To see if the data collection according to the protocol is feasible and to identify the problems to conduct further study. | — |
Secondary
| Measure | Time frame |
|---|---|
| Exploratory analysis on the relation between text analysis and diagnoses and/or symptom severity. | — |
Countries
Japan
Contacts
Public ContactTaishiro Kishimoto
Keio University School of Medicine Hills Joint Research Laboratory for Future Preventive Medicine and Wellnes
Outcome results
None listed