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Development and validation of a clinical prediction model for psychotic relapse within 12 months after discharge in people with schizophrenia

Development and validation of a clinical prediction model for psychotic relapse within 12 months after discharge in people with schizophrenia - Development and validation of a clinical prediction model for psychotic relapse within 12 months after discharge in people with schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000043345
Enrollment
800
Registered
2021-02-20
Start date
2020-12-22
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 and related disorders

Interventions

None listed

Sponsors

Department of Health Promotion and Human Behavior, Kyoto University School of Medicine
Lead Sponsor
Isogaya Hospital Urawa Shinkei Sanatorium Chiba Psychiatric Medical Centre Tsukuba University (We did not recruit participants at Wakamiya Hospital and Iwate Prefecture Nanko Hospital. Sep/13/2023)
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who were discharged from one of five participating hospitals between January 2014 and December 2018 will be included if they were diagnosed as one of the following (ICD-10 code in the parentheses): - Schizophrenia (F20) - Schizotypal disorder (F21) - Persistent delusional disorders (F22) - Acute and transient psychotic disorders (F23) - Induced delusional disorder (F24) - Schizoaffective disorders (F25) - Other nonorganic psychotic disorders (F28) - Unspecified nonorganic psychosis (F29)

Exclusion criteria

Exclusion criteria: Patients with the following conditions will be excluded: - Those who had been enrolled in this study with a previous episode of hospitalisation due to psychosis (i.e. a patient cannot be enrolled more than once during the study period) - Those with substance/medication-induced psychosis - Those with psychosis due to another medical condition, including peri-and postpartum psychosis and psychosis in dementia - Those with diagnosis in the inclusion criteria whose admission are not due to psychosis as judged by one of investigators - Those with diagnosis in the inclusion criteria with which one of investigators disagree due to the lack of sound reasoning - Those discharged from a non-acute ward - Those with a plan to be readmitted in the short period of time - Those with ambiguous diagnosis as judged by one of investigators - Those discharged to another psychiatric hospital - Those discharged to medical hospital

Design outcomes

Primary

MeasureTime frame
Psychotic relapse as a composite outcome defined by an occurrence of any one of the following: psychiatric hospitalisation, psychiatrist's decision that hospitalisation is required, an increase in antipsychotic dosage, an increase in the level of psychiatric care, and violence to self and/or others. Participants will be followed up up to 12 months after their discharge from the index hospitalisation.

Secondary

MeasureTime frame
Psychiatric hospitalisation due to psychotic relapse

Countries

Japan

Contacts

Public ContactAkira Sato

Kyoto University School of Medicine Department of Health Promotion and Human Behavior

sato.akira.57m@st.kyoto-u.ac.jp080-3475-7068

Outcome results

None listed

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