Development of software to enable screening and severity assessment of the depression recovery process

Not Applicable

Recruiting

• Conditions: As described in the inclusion criteria; Depressive Disorder; D003866

• Registration Number: JPRN-jRCT1031220528
• Lead Sponsor: Kikuchi Toshiaki

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-12-23
• Last Update Posted: 1 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

1) Patients clinically diagnosed with a depressive disorder group according to DSM-5 criteria, who have completed the acute phase of treatment and are in symptomatic remission or are 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 11.0 or later or Android version 5.0 or later)

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.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Well-being<br>Depressive symptoms<br>Quality of life<br>Recurrence<br> Remission<br>Recovery state

Secondary Outcome Measures

Name	Time	Method
Visualization of recurrence of mental illness<br>The relationship between depressive symptoms and work engagement evaluation indices, etc.