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Trial registered on ANZCTR
Registration number
ACTRN12620001340921
Ethics application status
Approved
Date submitted
21/09/2020
Date registered
14/12/2020
Date last updated
29/10/2021
Date data sharing statement initially provided
14/12/2020
Type of registration
Retrospectively registered
Titles & IDs
Public title
Parental and Healthcare Professional Concern in the Diagnosis of Paediatric Sepsis
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Scientific title
Parental and Healthcare Professional Concern in the Diagnosis of Paediatric Sepsis: A Prospective Multicentre Observational Study
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Secondary ID [1]
301941
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Nil known
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Universal Trial Number (UTN)
U1111-1256-4537
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Trial acronym
Nil
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Paediatric Sepsis
318486
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Serious Bacterial Infection
318487
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Condition category
Condition code
Infection
316489
316489
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0
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Studies of infection and infectious agents
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Determining diagnostic accuracy of concern levels in parents, doctors and nurses to recognise paediatric sepsis by study-specific questionnaire completion. This will take place in children being screened for sepsis and/or having biobanking completed (a single blood sample) at two large tertiary sites. The surveys will be distributed to one of the child’s parents/caregiver’s, nurse and doctor on presentation and will be completed during ED stay (observation session). Surveys will aim to be completed at time closest to triage and within 4-hrs from initial presentation. All eligible participants where prospective consent is obtained will be given a study-specific questionnaire containing up to seven questions where they will rate their level of concern, to which they agree or disagree with a statement or question using a 5 point likert scale followed by two free text questions requesting information on symptoms and symptoms most concerning. Both medical officer and nurse caring for the child will receive a study specific survey one for medical, one for nurses, containing six questions to complete. It is anticipated the questionnaire takes no longer then five minutes to complete over a single session. The questionnaire will be handed to the medical officer, nurse and parent by either a research nurse or initiated by the clinician caring for the child if outside research team hours.
To ensure consistent comparison, all surveys have the same basic design and content, with minor adaptions to reflect the participant role (parent vs nurse vs doctor).
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Intervention code [1]
318229
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Early Detection / Screening
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Suspected or proven infection in presence of organ dysfunction, defined as a pSOFA score >0 at time of assessment will be determined through linkage with medical records and pathology reports. A linear mixed effects model will be performed to assess the associations between the questionnaires assessing concern and the primary outcome.
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Assessment method [1]
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Timepoint [1]
324633
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Primary timepoint 1 for pSOFA score calculation will be determined at time closet to survey completion.
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Secondary outcome [1]
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Suspected or proven infection and development of organ dysfunction, defined as a pSOFA score >0, within 48hours of presentation will be determined based on the review of organ dsyfunction through linkage with medical records and pathology reports. A linear mixed effects model will be performed to assess the associations between the questionnaire assessing concern and the secondary outcomes.
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Assessment method [1]
385285
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Timepoint [1]
385285
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Within 48 hours from initial presentation
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Secondary outcome [2]
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Confirmed or probable bacterial infection independent of organ dysfunction, within 48 hours of presentation determined through linkage with medical records and pathology reports.
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Assessment method [2]
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Timepoint [2]
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Within 48 hours from initial presentation
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Secondary outcome [3]
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Inter-rater reliability will be conducted and reported on for each rater (doctor, nurse & parent) against the primary and secondary outcomes
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Assessment method [3]
389485
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Timepoint [3]
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At time of survey completion
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Eligibility
Key inclusion criteria
Child aged >30 days and <18 years old, presenting to the emergency department evaluated for sepsis on the sepsis pathway and/or having blood culture sampling, survey will aim to be completed at time closest to triage and within 4 hours from initial presentation, must be within ED stay, parent/caregiver and/or treating doctor and/or nurse available for survey.
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Minimum age
30
Days
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Maximum age
18
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Parents who speak languages other than English, children with high suspicion of SARS-CoV-2, patients in clinical areas outside the ED such as ward or Paediatric Intensive Care Unit
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Study design
Purpose
Screening
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Duration
Cross-sectional
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Descriptive analysis of demographics and baseline patient features of children which have had surveys completed
Exploratory factor analysis
Linear mixed effects model
Regression analysis
Qualitative data will be analysed using the Framework Method
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
20/12/2018
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Date of last participant enrolment
Anticipated
1/02/2021
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Actual
20/10/2020
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Date of last data collection
Anticipated
1/02/2021
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Actual
27/11/2020
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Sample size
Target
400
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Accrual to date
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Final
533
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment hospital [1]
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Queensland Children's Hospital - South Brisbane
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Recruitment hospital [2]
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Gold Coast University Hospital - Southport
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Recruitment postcode(s) [1]
30897
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4101 - South Brisbane
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Recruitment postcode(s) [2]
30898
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4215 - Southport
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Funding & Sponsors
Funding source category [1]
306357
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Charities/Societies/Foundations
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Name [1]
306357
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Emergency Medicine Foundation (EMF)
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Address [1]
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Suite 1b, Terraces, 19 Lang Parade Milton QLD, 4064
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Country [1]
306357
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Australia
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Primary sponsor type
University
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Name
University of Qld
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Address
St Lucia, QLD. 4072
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Country
Australia
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Secondary sponsor category [1]
307624
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None
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Name [1]
307624
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Address [1]
307624
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Country [1]
307624
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
306565
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Childrens Health Queensland Human Research Ethics Comittee
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Ethics committee address [1]
306565
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Centre for Children's Health Research, Queensland Children's Hospital Precinct, Level 7, 62 Graham Street, South Brisbane, QLD, 4101
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Ethics committee country [1]
306565
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Australia
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Date submitted for ethics approval [1]
306565
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03/06/2017
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Approval date [1]
306565
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25/11/2017
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Ethics approval number [1]
306565
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HREC/17/QRCH/85, Amendment: 03
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Summary
Brief summary
The primary purpose of this study is to determine if the level of concern of parents and healthcare workers, within the emergency setting, can help improve diagnostic accuracy for paediatric sepsis.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Ms Amanda Harley
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Address
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501 Stanley St, South Brisbane QLD 4101
Paediatric Critical Care Research Group, Centre for Children's Health Research
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Country
104302
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Australia
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Phone
104302
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+61 417626323
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Fax
104302
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Email
104302
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[email protected]
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Contact person for public queries
Name
104303
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Amanda Harley
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Address
104303
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501 Stanley St, South Brisbane QLD 4101
Paediatric Critical Care Research Group, Centre for Children's Health Research
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Country
104303
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Australia
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Phone
104303
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+61 417626323
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Fax
104303
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Email
104303
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[email protected]
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Contact person for scientific queries
Name
104304
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Amanda Harley
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Address
104304
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501 Stanley St, South Brisbane QLD 4101
Paediatric Critical Care Research Group, Centre for Children's Health Research
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Country
104304
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Australia
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Phone
104304
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+61 417626323
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Fax
104304
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Email
104304
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
Will re-assess upon study completion
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
10025
Ethical approval
Within published manuscript
[email protected]
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Impact of parental and healthcare professional concern on the diagnosis of pediatric sepsis: a diagnostic accuracy study.
2023
https://dx.doi.org/10.3389/fped.2023.1140121
N.B. These documents automatically identified may not have been verified by the study sponsor.
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