UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000040589
Receipt number R000046323
Scientific Title Physical Restraints in Critically Ill Children: Multicenter Longitudinal Point Prevalence Study
Date of disclosure of the study information 2020/05/30
Last modified on 2020/05/30 04:05:52

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Basic information

Public title

Physical Restraints in Critically Ill Children: Multicenter Longitudinal Point Prevalence Study

Acronym

PRINCE Study

Scientific Title

Physical Restraints in Critically Ill Children: Multicenter Longitudinal Point Prevalence Study

Scientific Title:Acronym

PRINCE Study

Region

Japan


Condition

Condition

critically ill or injured children

Classification by specialty

Pediatrics Intensive care medicine Nursing

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To explore the prevalence of and associated factors with physical restraints in critically ill children in Japan.

Basic objectives2

Others

Basic objectives -Others

To explore the prevalence of and associated factors with physical restraints in critically ill children in Japan.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Prevalence and the characteristics of the physically restrained critically ill or injured children.

Key secondary outcomes

Factors associated with physical restraints.


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

1 months-old <=

Age-upper limit

120 months-old >

Gender

Male and Female

Key inclusion criteria

Aged 1 month to 10-years-old children in ICUs.

Key exclusion criteria

1) over 10-year-old children
2) newborn
3) without consent

Target sample size

150


Research contact person

Name of lead principal investigator

1st name Ryo
Middle name
Last name Ikebe

Organization

Osaka Womens and Childrens Hospital

Division name

Department of Nursing

Zip code

594-1101

Address

840, Murodocyo, Izumi, Osaka

TEL

0725-56-1220

Email

rikebe@wch.opho.jp


Public contact

Name of contact person

1st name Ryo
Middle name
Last name Ikebe

Organization

Osaka Womens and Childrens Hospital

Division name

Department of Nursing

Zip code

594-1101

Address

840, Murodocyo, Izumi, Osaka

TEL

0725-56-1220

Homepage URL


Email

rikebe@wch.opho.jp


Sponsor or person

Institute

Osaka Womens and Childrens Hospital

Institute

Department

Personal name



Funding Source

Organization

Japan Society for the Promotion of Science Grant-in-Aid for Scientific Research

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethical Review Board of Osaka Womens and Childrens Hospital

Address

840, Murodocyo, Izumi, Osaka

Tel

0725-56-1220

Email

rikebe@wch.opho.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2020 Year 05 Month 30 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled

398

Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2018 Year 10 Month 20 Day

Date of IRB

2018 Year 11 Month 30 Day

Anticipated trial start date

2019 Year 03 Month 04 Day

Last follow-up date

2019 Year 11 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Multicenter longitudinal point prevalence study


Management information

Registered date

2020 Year 05 Month 30 Day

Last modified on

2020 Year 05 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046323


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name