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Clinical Trials in South Korea / NCT07128446
Recruiting Not applicable

COPM-Based Goal Setting Strategies in the PICU

NCT07128446 · tracked via the Priya Life Science South Korea tracker
Phase
Not applicable
Started
2025-08-29
Last updated
2026-03-10

Condition(s) studied

Critical IllnessPediatric Intensive Care Unit

Investigational drug(s) / intervention(s)

Standard physical and occupational therapy

Standard physical and occupational therapy: Participants admitted to the Pediatric Intensive Care Unit (PICU) will receive standard occupational therapy as part of routine clinical care. Interventions will be tailored to each patient's medical status and functional needs and may include activities of daily living (ADL) training, positioning, range of motion exercises, sensory stimulation, and caregiver education. No additional experimental treatment will be introduced for study purposes. The primary focus of the study is to evaluate patient-centered outcomes using the Canadian Occupational Performance Measure (COPM), without altering the standard therapeutic approach.

Study summary

COPM-Based Goal Setting Strategies in the PICU

Eligibility

Sex
ALL
Min age
1 Year
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: Phase 1-2 (Delphi Survey - Experts) * Physicians specializing in pediatrics or physical medicine and rehabilitation, occupational therapists, physical therapists, and nursing staff * Minimum of 2 years of direct clinical experience in a Pediatric Intensive Care Unit (PICU) Phase 3 (Pilot Testing - Caregivers \& PICU Clinicians) Caregivers: * Legal guardian of a child aged 1-18 years admitted to PICU * ≥24 hours post-admission PICU clinicians: \- Treating occupational or physical therapist involved in the child's care during PICU admission Exclusion Criteria: Phase 1-2 (Delphi Survey - Experts) * Rehabilitation professionals without prior PICU clinical experience * Inability to read or respond to Korean-language surveys Phase 3 (Pilot Testing - Caregivers \& PICU Clinicians) * Caregivers experiencing severe emotional distress, or deemed inappropriate for participation by the treating clinician * Non-Korean-speaking caregivers * Refusal or withdrawal of informed consent at any stage

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Samsung Medical Center Seoul Gangnam-gu Recruiting
Samsung Medical Center Seoul South Korea Not Yet Recruiting

More Samsung Medical Center trials in South Korea

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07128446 on ClinicalTrials.gov ↗ ← All trials in South Korea