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A Korean Point Prevalence Study of Acute Rehabilitation for Kids in the PICU (PARK-PICU)

1. juni 2026 oppdatert av: Jeong Yi Kwon, Samsung Medical Center

Prevalence of Acute Rehabilitation for Kids in the Pediatric Intensive Care Unit

This study investigates the prevalence of acute rehabilitation practices among children in pediatric intensive care units (PICUs).

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

This is a prospective observational study conducted across 13 hospitals. Data will be collected at three predefined time points to assess the prevalence of acute rehabilitation practices among children in pediatric intensive care units.

Studietype

Observasjonsmessig

Registrering (Antatt)

396

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

  • Sør -Korea
    • Daegu
      • Daegu, Daegu, Sør -Korea, 41404
        • Kyungpook National University Chilgok Hospital
        • Ta kontakt med:
    • Daejeon
      • Daejeon, Daejeon, Sør -Korea, 35015
        • Chungnam National University Hospital
        • Ta kontakt med:
    • Gyeonggi-do
      • Seongnam-si, Gyeonggi-do, Sør -Korea, 13620
        • Seoul National University Bundang Hospital
        • Ta kontakt med:
    • Gyeongsangnam-do
      • Yangsan, Gyeongsangnam-do, Sør -Korea, 50612
        • Pusan National University Yangsan Hospital
        • Ta kontakt med:
    • Incheon
      • Incheon, Incheon, Sør -Korea, 22332
        • Inha University Hospital
        • Ta kontakt med:
    • Jeju-do
      • Jeju City, Jeju-do, Sør -Korea, 63241
        • Jeju National University Hospital
        • Ta kontakt med:
    • Jeollabuk-do
      • Jeonju, Jeollabuk-do, Sør -Korea, 54907
        • Jeonbuk National University Hospital
        • Ta kontakt med:
    • Jeollanam-do
      • Hwasun, Jeollanam-do, Sør -Korea, 58128
        • Chonnam National University Hwasun Hospital
        • Ta kontakt med:
    • Seoul
      • Seoul, Seoul, Sør -Korea, 03080
        • Seoul National University Hospital
        • Ta kontakt med:
      • Seoul, Seoul, Sør -Korea, 05505
        • Asan Medical Center
        • Ta kontakt med:
      • Seoul, Seoul, Sør -Korea, 06351
        • Samsung Medical Center
        • Ta kontakt med:
      • Seoul, Seoul, Sør -Korea, 03722
        • Severance Hospital
        • Ta kontakt med:
      • Seoul, Seoul, Sør -Korea, 06591
        • Seoul St. Mary'S Hospital
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen

Tar imot friske frivillige

N/A

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

The study population includes critically ill children and adolescents aged 18 years or younger who are admitted to pediatric intensive care units (PICUs) at participating hospitals in South Korea. Patients who have been hospitalized in the PICU for at least 72 hours as of 9:00 AM on predefined study dates will be included. All eligible patients at each study time point will be included to reflect real-world clinical practice in pediatric critical care.

Beskrivelse

Inclusion Criteria:

  • Children and adolescents aged 18 years or younger who have been admitted to the pediatric intensive care unit (PICU) for at least 72 hours as of 9:00 AM on the predefined study date at participating hospitals.

Exclusion Criteria:

  • No exclusion criteria. All eligible patients meeting the inclusion criteria will be included to comprehensively assess the real-world prevalence of acute rehabilitation practices and associated barriers in pediatric intensive care units.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
Children in Pediatric Intensive Care Units
Children admitted to pediatric intensive care units (PICUs) who are assessed for the prevalence of acute rehabilitation practices during critical care.
Annen: Acute Rehabilitation (Observed Practice)
This study does not assign any interventions. It observes routine clinical practices of acute rehabilitation provided to children in pediatric intensive care units as part of standard care.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Proportion of Participants Who Received Acute Rehabilitation
Tidsramme: At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period
Prevalence is defined as the proportion of eligible children in the pediatric intensive care unit who received at least one session of physical therapy or occupational therapy within the 24 hours preceding each study assessment point.
At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Number of Acute Rehabilitation Sessions per Participant
Tidsramme: At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period
The number of physical therapy or occupational therapy sessions delivered to eligible children within the 24 hours preceding each assessment point.
At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period
Number of Participants by Type of Rehabilitation Intervention
Tidsramme: At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period
The types of rehabilitation interventions delivered within the 24 hours preceding each assessment point, including passive exercise, active exercise, positioning, mobility training, and occupational therapy interventions.
At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period
Proportion of sessions Involving Assistive Devices
Tidsramme: At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period
The proportion of rehabilitation sessions involving assistive devices or equipment during the 24 hours preceding each assessment point.
At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period
Number of Sessions by Delivery Method
Tidsramme: At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period
The types of rehabilitation delivery methods used within the 24 hours preceding each assessment point, including bedside therapy, in-room mobilization, and therapist-assisted mobility interventions.
At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period
Odds Ratios for Factors Associated With Absence of Acute Rehabilitation
Tidsramme: At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period
Multivariable logistic regression analysis will be performed to evaluate clinical and organizational factors associated with the absence of acute rehabilitation delivery among eligible children in the pediatric intensive care unit. Predictor variables will include patient demographics, severity of illness, sedation status, mechanical ventilation, restraint use, ICU structure, rehabilitation protocols, and staffing resources.
At three seasonal point-prevalence assessments conducted approximately 6 months apart over an 18-month period

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Samsung Medical Center

Samarbeidspartnere

Johns Hopkins University

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

28. mai 2026

Primær fullføring (Antatt)

31. mai 2027

Studiet fullført (Antatt)

31. desember 2027

Datoer for studieregistrering

Først innsendt

13. mai 2026

Først innsendt som oppfylte QC-kriteriene

1. juni 2026

Først lagt ut (Faktiske)

5. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

5. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

1. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Nøkkelord

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • 2026-03-006

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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