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An exploratory study of factors associated with the development of post-intensive care syndrome

An exploratory study of factors associated with the development of post-intensive care syndrome - An exploratory study of factors associated with the development of post-intensive care syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000045737
Enrollment
200
Registered
2021-10-12
Start date
2021-11-01
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

Critical Care Medicine

Interventions

None listed

Sponsors

Tokyo Women's Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients over 20 years of age at the time of consent Patients who can communicate in Japanese Patients who entered the ICU and stayed for 72 hours or more Patients who received sufficient explanation before participating in this study, and after sufficient understanding, obtained the voluntary written consent of the patient (or a substitute if necessary). Patients who meet all of the above are targeted.

Exclusion criteria

Exclusion criteria: Patients with advanced cognitive dysfunction Patients with brain injury (anaerobic brain injury, stroke, traumatic brain injury) before and during ICU admission Patients after organ transplantation Patients expected to die within 3 months of discharge Patients with unstable mental illness Other patients who the principal investigator deems inappropriate as a subject

Design outcomes

Primary

MeasureTime frame
Percentage of PICS 6 months after discharge of patients admitted to the ICU

Secondary

MeasureTime frame
Sleep status (objective data by brain wave measurement type sleep measurement, subjective data by questionnaire) Onset and duration of delirium (days) Length of stay in ICU Number of days of hospitalization after leaving the ICU Length of hospitalization Scores for each scale related to physical function, depression, traumatic stress symptoms, physical symptoms, fatigue, subjective insomnia severity, and cognitive function. Outcome after 6 months, outcome after 2 years (re-hospitalization and death)

Countries

Japan

Contacts

Public ContactNobuo Sato

Tokyo Women's Medical University Department of Intensive Care Medicine

nsato-nst@umin.ac.jp03-3353-8111

Outcome results

None listed

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