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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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JPRN |
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Last refreshed on:
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17 October 2023 |
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Main ID: |
JPRN-UMIN000027080 |
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Date of registration:
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21/04/2017 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Quantifying Psychiatric Disorders with Natural Language Processing: A Pilot Study
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Scientific title:
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Quantifying Psychiatric Disorders with Natural Language Processing: A Pilot Study - Natural Language Processing for Psychiatric disorders: A Pilot Study |
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Date of first enrolment:
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2017/04/21 |
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Target sample size:
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30 |
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Recruitment status: |
Complete: follow-up continuing |
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URL:
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https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000030791 |
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Study type:
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Observational |
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Study design:
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Not selected Not selected
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Phase:
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Not selected
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Countries of recruitment
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Japan
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Contacts
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Name:
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Taishiro
Kishimoto |
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Address:
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35 Shinanomachi, Shinjuku-ku, Tokyo, JAPAN
Japan |
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Telephone:
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03-5363-3971 |
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Email:
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tkishimoto@keio.jp |
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Affiliation:
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Keio University School of Medicine Department of Neuropsychiatry |
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Name:
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Taishiro
Kishimoto |
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Address:
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Roppongi Hills North Tower 7F, 6-2-31 Roppongi, minato-ku, Tokyo, Japan
160-8582
Japan |
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Telephone:
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03-5786-0006 |
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Email:
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tkishimoto@keio.jp |
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Affiliation:
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Keio University School of Medicine Hills Joint Research Laboratory for Future Preventive Medicine and Wellnes |
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Key inclusion & exclusion criteria
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Inclusion 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.
Age minimum:
20years-old
Age maximum:
Not applicable
Gender:
Male and Female
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Health Condition(s) or Problem(s) studied
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1. Patients with major depressive disorder, bipolar I/II disorder, schizophrenia, anxiety disorders, and major/mild neurocognitive disorder by DSM-5 2. Healthy volunteers
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Primary Outcome(s)
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To see if the data collection according to the protocol is feasible and to identify the problems to conduct further study.
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Secondary Outcome(s)
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Exploratory analysis on the relation between text analysis and diagnoses and/or symptom severity.
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Source(s) of Monetary Support
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Japan Science and Technology Agency (JST)
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Ethics review
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Status: YES
Approval date: 30/03/2017
Contact:
med-rinri-jimu@adst.keio.ac.jp
The Clinical and Translational Research Center
03-3353-1211
med-rinri-jimu@adst.keio.ac.jp
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Results
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Results available:
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Yes |
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Date Posted:
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Date Completed:
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28/02/2022 |
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URL:
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