The clinical feasibility of a system for optimizing depression treatment

Not Applicable

• Conditions: depression

• Registration Number: JPRN-UMIN000052445
• Lead Sponsor: Keio University School of Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-10-10
• Last Update Posted: 17 October 2023
• Study Completion: 2028-03-30

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Not provided

Exclusion Criteria

Research Physician: Of the cases meeting the above eligibility criteria, those who meet any of the following conditions will be excluded from participation in this study. (i) Those who cannot use a personal computer, smartphone, etc. (ii) Other persons deemed by the principal investigator to be ineligible for the study (e.g., employed by the principal investigator, etc.) Research Patients: Of the patients who meet the above eligibility criteria, those who meet any of the following conditions will be excluded from participation in this study. (i) Patients with a history of severe organic brain lesions or cognitive dysfunction. (ii) Patients with a clinical diagnosis of a serious or unstable life-threatening physical condition at the time of screening. (iii) Other subjects who are judged by the principal investigator to be ineligible for this study.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Physicians' difficulty and 3-month retention rate in using the tool

Secondary Outcome Measures

Name	Time	Method
For physicians: compliance with the recommended treatment during the 3-month period, expected number of subjects who will use the tool, and contribution to treatment selection. For patients: degree of difficulty in reporting symptoms and of satisfaction with treatment