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Clinical Trials/ISRCTN23547970
ISRCTN23547970
Completed
未知

A feasibility randomised controlled trial investigating the clinical and cost effectiveness of a complex intervention to improve the management of children presenting to primary care with acute respiratory tract infection

niversity of Bristol (UK)0 sites500 target enrollmentJune 27, 2014

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity of Bristol (UK)
Enrollment
500
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 27, 2014
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Bristol (UK)

Eligibility Criteria

Inclusion Criteria

  • Clinicians:
  • GPs and prescribing nurses are eligible to recruit children to the study
  • GP practices will be included if they have at least Internet Explorer version 8 on their IT systems
  • Children can be included into the study if they meet the following criteria:
  • 1\. Children aged \=3 months and \<12 years
  • 2\. Presenting with an acute RTI with cough for \=28 days as a main symptom (including exacerbation of asthma)
  • 3\. Presenting with illnesses such as RTI and epilepsy or diabetes, including infective exacerbation of asthma (non\-infective exacerbation of asthma is an exclusion criterion)
  • Target Gender: Male \& Female; Upper Age Limit 11 years ; Lower Age Limit 3 months

Exclusion Criteria

  • Children will not be eligible for the study if:
  • 1\. They are aged \< 3 months or \= 12 years
  • 2\. The parent/carer/children are unable or unwilling to assist with study
  • 3\. The child has already been successfully recruited to the CHICO study
  • 4\. They present with acute non\-infective exacerbations of asthma
  • 5\. They present with RTI without cough or symptoms \>28 days
  • 6\. They are at greater risk of serious infection; they have chronic diseases/multi\-morbidities that increase the risk of RTI complications

Outcomes

Primary Outcomes

Not specified

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