Major Depressive Disorder
Conditions
Interventions
None listed
Sponsors
National Center of Neurology and Psychiatry
Aoyama Gakuin University Himorogi Psychiatric Institute Kyorin University Hospital Keio University Hospital Tokyo Women'
s Medical University Medical Center East
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patients diagnosed by the attending physician with DSM-5 as the first depressive episode without psychotic symptoms or recurrent major depressive disorder (whether inpatient or outpatient) 2) Those who are 20 years old or older and 65 years old or younger when consent is obtained 3) Those who can obtain written informed consent after understanding the contents of this research
Exclusion criteria
Exclusion criteria: 1) Patients diagnosed with substance use disorders 2) Patients with a history of head injury accompanied by consciousness loss 3) Individuals judged unsuitable by the attending physician for carrying out the observation, evaluation, and examination prescribed in this study. 4) Individuals judged by the attending physician to worsen the original disease by participating in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Consistency between face-to-face MADRS evaluation (facility rating) and remote evaluation via information and communication equipment (central rating) | — |
Secondary
| Measure | Time frame |
|---|---|
| Inter-rater reliability | — |
Countries
Japan
Contacts
Public ContactYasunori Morio
National Center of Neurology and Psychiatry Translational Medical Center
Outcome results
None listed