Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12609000042246
Ethics application status
Approved
Date submitted
29/09/2008
Date registered
19/01/2009
Date last updated
14/11/2018
Date data sharing statement initially provided
14/11/2018
Type of registration
Retrospectively registered

Titles & IDs
Public title
Trial of a computer decision support system and structured medical assessment for children with a febrile illness presenting to the Emergency Department of The Children's Hospital at Westmead
Scientific title
Febrile children less than 5 years with a febrile illness are assesed by doctors using either a computer decision support system, a structured febrile assessment tool or standard care for the diagnosis of pneumonia, urinary tract infection or bacteraemia
Secondary ID [1] 296602 0
nil known
Universal Trial Number (UTN)
Trial acronym
FEVER
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Febrile illness 3767 0
Condition category
Condition code
Infection 3942 3942 0 0
Other infectious diseases

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
The computer decision support system (Intervention 1.) graphically displays the risk of pneumonia, urinary tract infection and bacteraemia in individual children after a structured assessment. The intervention also includes recommendations for further testing and antibiotic use.
The computer decision support system is a graphical display of a diagnostic algorithm that is based on clinical findings collected in a mandatory structured medical assessment tool, completed by the Emergency department doctor assessing the febrile child. The structured medical assessment consists of 40 stem questions and 25 conditional questions about past medical history, current illness history, clinical observations, physical examination and vaccination status. The structured assessent is completed at the time the child is seen by the Emergency Department (ED) doctor. The structured assessment takes between 5 and 15 minutes to complete depending on responses and doctor familiarity with the tool. The computer decision support system is on a computer screen that appears after completion of the structured assessment tool. doctors can close the screen immediately or review it as long as desired. Intervention 2 is the structured medical assessment tool identical to that used in Intervention 1.
Intervention code [1] 3478 0
Diagnosis / Prognosis
Comparator / control treatment
Intervention 1 will be compared with Intervention 2 and also compared with standard care. Standard care involves doctors completing their assessment and recording what details they consider important.
Control group
Active

Outcomes
Primary outcome [1] 4840 0
Appropriate antibiotic use. Results of urine culture, blood culture and chest x rays done at The Childrens Hospital at Westmead (CHW) and other health carers will determine disease positive or negative. Antibiotic use is collected from ED medical notes and asking parents at follow-up. Diagnoses of non-serious bacterial illness is collected from ED medical notes.
Timepoint [1] 4840 0
At the time of the febrile illness. Measured once for each febrile illness, children may present more than once during the study period with a febrile illness. The study period is 2 years, 20th February 2007 to 19th February 2009
Secondary outcome [1] 8167 0
Frequency of relevant investigations (chest x-rays, urine cultures, blood culture). Measured once for each febrile illness.
Timepoint [1] 8167 0
Measured once for each febrile illness during the study period.
Secondary outcome [2] 8168 0
Representation to The Childrens Hospital at Westmead Emergency Department with the same febrile illness. A visit for the same illness is defined as one within 24 hours of a previous visit, or, a visit in which the child had not been febrile for < 24 hours between the two visits. The afebrile period is determined from review of clinical notes and direct questioning of parents at 10-14 day followup.
Timepoint [2] 8168 0
At the time of the febrile illness. Measured once for each febrile illness.
Secondary outcome [3] 8169 0
Admission. The number of admissions to a hospital ward for managament of the Admission details are electronically extracted from the Childrens' Hospital admissions database. Parents are questioned about other health care facilities attended when they are contacted at the 10-14 day follow-up. The average duration of the stay in a hospital ward for management of the febrile illness will be calculted from all admissions during the period.
Timepoint [3] 8169 0
Measured once, at the time of the febrile illness.
Secondary outcome [4] 8170 0
Antibiotics. The total number of episodes that were given antibiotics while the child was in the Emergency Department. The total number of episodes where the antibiotics given in ED were via intravenous (IV) route. The total number of episodes where the antibiotics given in ED were via oral route. The total number of episodes where each different type of antibiotic was used. Antibiotic use is collected from details recorded in the electronic medical record of the child and from direct questioning of parents at time of 10-14 day follow-up. Contradiction between the two responses is resolved by weighting clinical documents over parental recall.
Timepoint [4] 8170 0
Measured once, at the time of the febrile illness.
Secondary outcome [5] 8171 0
Illness Duration. Average duration of illness
Average duration of fever. Parents are contacted at 10-14 days after presentation to The Childrens Hospital Emergency Department and questioned about current health status of their child, when the child became fever free and when the child was well again. Time periods are grouped into morning, day and eveing time slots for simpler recall. Duration calculations use designated times for each period to calculate duration since Emergency department presentation ( a field electronical downloaded from the Emergency department database).
Timepoint [5] 8171 0
Measured one, at the time of the febrile illness.
Secondary outcome [6] 8172 0
Health-care facility utilization. Total number of episodes where the child was taken to see a general practitioner (GP) or other health care provider. Total number of episodes where the child was taken to another hospitals Emergency department. Total number of episodes where the childs GP or other health care provider performed a reference test of interest to the study (Chest x ray, blood culture, urine culture). Total number of episodes where the childs GP or other health care provider prescribed antibiotics
Timepoint [6] 8172 0
At the time of the febrile illness during the study period; 20th February 2007 to 19th February 2009. At 10-14 day follow-up parents are contacted by telephone and asked about attendance at other health care facilties and what tests and medical treatments were performed.

Eligibility
Key inclusion criteria
Children less than 5.0 years at presentation to The Childrens Hospital at Westmead Emergency Department, presenting for assessment of a febrile illness. A febrile illness is defined as; A preseting problem recorded by a triage nurse as relating to fever (ICD10AM codes R50.0, R50.1, R50.9, R56.0), or A positive response to the triage questions; Has your child felt hot in the past 24 hours? or Has your child’s temperature been taken in the past 24 hours?, (yes) and the response options 38.0 – 38.9oC or 39.0 – 39.9oC or > 40.0oC are chosen OR Nurse measured temperature of =38.0 o C recorded in Observation screen/notes
Minimum age
0 Days
Maximum age
5 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Children greater than 5.0 years of age at presentation
Children transferred in from another hospital (assessed elsewhere and transferred here from another facility)
Children with a reference test result performed less than 24 hours prior to ED presentation for the current illness (ie urine, blood, CSF, joint/fluid cultures, chest x ray, bone scan as detailed in the ED Summary)
Children presenting as a child protection unit case (ie suspected child abuse as detailed in ED Summary)
Children currently or previously treated for cancer (as detailed in ED Summary)
Children on immunosuppression therapy or with a primary immunodeficiency (as detailed in ED summary)
Children who present with a new burn injury (ie the reason for the visit) and who trigger the study only because they 'Felt Hot' and have no other indications that the visit is related to a febrile illness

Study design
Purpose of the study
Diagnosis
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Cluster randomised trial. Each Emergency Department doctor is a cluster. Junior doctors are randomly allocated to one of the three intervention arms the first time they login to the Emergency Department electronic medical record database and remove an eligible febrile child from the waiting list. Each doctor remains in the allocated group for the duration of their time at The Children's Hospital at Westmead. Emergency Department consultants and Emergency Department Fellows are randomised from a separate computer generated list from junior doctors. These doctors were known at the start of the study and their computer login names were entered manually into the Emergency Department database but without knowledge of the randomised allocation list. This separate randomisation list was necessary to ensure a balance of allocations for the much smaller group of highly experience senior Emergency departent staff.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated randomised list.
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
20/02/2007
Actual
20/02/2007
Date of last participant enrolment
Anticipated
Actual
19/02/2009
Date of last data collection
Anticipated
Actual
20/05/2009
Sample size
Target
17000
Accrual to date
Final
17417
Recruitment in Australia
Recruitment state(s)
Recruitment postcode(s) [1] 1178 0
2145

Funding & Sponsors
Funding source category [1] 3939 0
Government body
Name [1] 3939 0
National Health and Medical Reserch Council
Country [1] 3939 0
Australia
Primary sponsor type
Hospital
Name
The Childrens Hospital at Westmead
Address
Locked bag 4001, Westmead, NSW 2145
Country
Australia
Secondary sponsor category [1] 3533 0
University
Name [1] 3533 0
The University of Sydney
Address [1] 3533 0
School of Public Health, Edward Ford Building A27, The University of Sydney, Camperdown, NSW 2006
Country [1] 3533 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 6006 0
The Childrens Hospital at Westmead Ethics Committee
Ethics committee address [1] 6006 0
Ethics committee country [1] 6006 0
Australia
Date submitted for ethics approval [1] 6006 0
14/08/2006
Approval date [1] 6006 0
12/09/2006
Ethics approval number [1] 6006 0
2006/076

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 28985 0
Prof Jonathan Craig
Address 28985 0
Centre for Kidney Research, The Childrens Hospital at Westmead, Locked bag 4001, westmead, NSW 2145
Country 28985 0
Australia
Phone 28985 0
0298451492
Fax 28985 0
Email 28985 0
[email protected]
Contact person for public queries
Name 12142 0
Professor Jonathan Craig
Address 12142 0
Centre for Kidney Research, The Childrens Hospital at Westmead, Locked bag 4001, westmead, NSW 2145
Country 12142 0
Australia
Phone 12142 0
+91 2 98453431
Fax 12142 0
+61 2 98451491
Email 12142 0
[email protected]
Contact person for scientific queries
Name 3070 0
Professor Jonathan Craig
Address 3070 0
Centre for Kidney Research, The Childrens Hospital at Westmead, Locked bag 4001, westmead, NSW 2145
Country 3070 0
Australia
Phone 3070 0
+61 2 98453431
Fax 3070 0
+61 2 98451491
Email 3070 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.