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A observational study using a wearable device in patients with schizophrenia

A observational study using a wearable device for patients with schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1080225178
Enrollment
20
Registered
2020-04-27
Start date
2020-06-03
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

schizophrenia

Interventions

Sponsors

Sumitomo Dainippon Pharma Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 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.

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
other The conseqtive days of wearing the devices and the rate of wearing the devices for each devices

Secondary

MeasureTime frame
other Change of the number of steps Sleep activity Questionnaire to patients CGI-S BPRS

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026