JPRN-jRCT1031210478招募中未知
Data collection and machine learning model development for depressive episode detection and severity assessment using wristband-type wearable device
Kikuchi Toshiaki0 个研究点目标入组 360 人开始时间: 2021年12月12日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 360
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- >= 18age old 至 ot applicable（—）
- 性别
- All
入选标准
- •In the case of patients
- •1) Patients clinically diagnosed as one of the following groups according to DSM-5 criteria: depressive disorders, bipolar and related disorders, anxiety disorders, obsessive-compulsive and related disorders, trauma- and stressor-related disorders, dissociative disorders, somatic symptom and related disorders, and have depressive symptoms, and are on outpatient or inpatient status at Keio University Hospital or research collaborating institutions.
- •Or, patients with clinically undiagnosed but depressive symptoms who are suspected to have depression (including depression in bipolar disorder) and who are outpatients or inpatients at Keio University Hospital or collaborating institutions.
- •2) Patients who are 18 years of age or older at the time of obtaining consent.
- •3) Patients for whom the attending physician judges that written consent can be obtained, or who can obtain consent from a substitute if the attending physician judges that it is difficult to obtain consent from the patient.
- •4) A person who owns and uses a smart phone (iOS 11.0 or later or Android version 5.0 or later)
- •In the case of a healthy person
- •1) A healthy person with no history of psychiatric illness who has volunteered to cooperate in the study (after obtaining consent, the M.I.N.I. will be used to confirm that the person does not have a psychiatric illness)
- •2) Age 18 years or older at the time of obtaining consent
- •3) Own and use a smart phone (iOS 11.0 or later or Android version 5.0 or later)
排除标准
- •In the case of patients
- •1) Patients who are judged by the attending physician to be mentally or physically overloaded by the measurements taken in this study, which may affect their medical conditions.
- •2) Patients suffering from comorbidities such as paralysis of the upper limbs that may affect the measurement results of the wristband wearable device.
- •3) Other patients deemed inappropriate by the principal investigator or sub-investigator.
- •In the case of healthy person
- •1) Persons suffering from comorbidities that may affect the measurement results of the wristband wearable device, such as paralysis of the upper limbs.
- •2) Others who are judged to be inappropriate by the principal investigator or sub-investigator
研究者
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