As described in the inclusion criteria Depressive Disorder/Bipolar and Related Disorder
Conditions
Interventions
None listed
Sponsors
Kikuchi Toshiaki
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patients who have been clinically diagnosed with depressive disorders, bipolar disorders and related disorders based on DSM-5 criteria, and who are either aiming for symptom remission after completing acute-phase treatment or undergoing maintenance treatment to prevent relapse 2) Patients who are at least 18 years of age at the time of consent 3) Patients whose attending physician determines that written consent can be obtained, or if the attending physician determines that obtaining consent from the patient is difficult, those who are able to obtain consent from a surrogate. 4) Persons who own and use a smartphone (iOS 17.0 or later or Android version 13.0 or later)
Exclusion criteria
Exclusion criteria: 1) Patients whose condition, in the judgment of the attending physician, could be affected by the mental or physical stress caused by the measurements in this study. 2) Patients with comorbidities that may affect the measurement results of the wristband wearable device, such as paralysis of the upper limbs. 3) Other patients deemed inappropriate by the principal investigator or co-investigators.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Well-being Depressive symptoms Quality of life Recurrence Remission Recovery state | — |
Secondary
| Measure | Time frame |
|---|---|
| Visualization of recurrence of mental illness The relationship between depressive symptoms and work engagement evaluation indices, etc. | — |
Contacts
Public ContactShotaro Kinoshita
Keio university school of medicine
Outcome results
None listed