跳至主要内容
临床试验/JPRN-jRCT1080225178
JPRN-jRCT1080225178已完成Unknown

A observational study using a wearable device for patients with schizophrenia

Sumitomo Dainippon Pharma Co., Ltd.0 个研究点目标入组 20 人开始时间: 2020年4月27日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
入组人数
20

研究概览

简要总结

20 subjects were randomized to A group (10 subjects) and B group (10 subjects). The conseqtive days (mean) of wearing devices were 9.8 days and 3.4 days in A group and B group (same order hereunder) respectively. The rate (mean) of wearing the devices for each device were 79.6% and 36.3%.

研究设计

研究类型
Observational

入排标准

年龄范围
>= 18age old 至 <= 65age old(—)
性别
All

入选标准

  • •Inclusion Criteria:
  • •(1) Subjects who voluntarily provide written consent to participate in the study. If the subject is considered a minor at the time of collection of the informed consent, written consent will be obtained from a legally acceptable representative (guardian) in addition to that obtained from the subject.
  • •(2) Subject who has schizophrenia diagnosed by DSM-5, diagnostic criteria, and in the opinion of the Investigator has been clinically stable.
  • •(3) Subject who has CGI-S score>=3 at baseline.

排除标准

  • •Exclusion Criteria
  • •(1)Subjects who has DSM-5 diagnosis consistent with a DSM-5 diagnosis other than schizophrenia.

研究者

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