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Personalised Outcomes in Children With Recurrent Wheeze

Validation of a Patient-reported Outcome Measurement Tool

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03858010
Enrollment
500
Registered
2019-02-28
Start date
2021-08-13
Completion date
2022-06-05
Last updated
2022-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma in Children

Keywords

asthma

Brief summary

This project aims to develop a PROM for preschool children with recurrent wheeze. Nearly one third of children will have at least one episode of wheeze in the first five years of life. The majority of these children grow out of the condition in early school years. However, their families go through challenging times often with numerous emergency department admissions and hospitalizations. Hospital admission rates for preschool children with wheeze attacks remain high and are increasing in the UK. New treatments have become available, but although current treatments speed recovery from a wheeze attack, still many children visit hospitals for rescue medications and medical reviews. Recent Australian data show that one fourth of these children remain at emergency departments for a less than four hours period, suggesting that with better information and education, these children could have remained at home. Justification-Significance of the work By understanding what really matters for these families, clinicians and stakeholders will be better able to design interventions that will reduce the hospital attendances and admissions by empowering parents to manage their children's condition. More specifically, this tool will assist GPs identify which of these children need to be reviewed by specialists, aid holistic management, ensure interventions are meaningful for families and assess the benefits of novel treatments. Methodology The items of the questionnaire have been generated through discussions with families in a qualitative research study conducted by the research team. These items will be refined and the questionnaire will be tested with families in different healthcare settings. Researchers will assess how well this questionnaire is identifying the children who present with greater number of hospital admissions and will be benefited from suggested interventions. The data will be analysed and based on the results, amendments will be made to the questionnaire, which can will then be introduced in the routine management of these children.

Detailed description

The validation of the tool will take place at St Mary's Hospital. The questionnaire aims to measure 1. incidence of wheeze attacks and use of rescue medications 2. parental/caregiver perception of recurrent wheeze control 3. parental/caregiver perception of effect of recurrent wheeze on family/child quality of life Participants will be given the questionnaire at the emergency departments or outpatients clinics following having consented to the study and will be asked to fill in the questionnaire and return it to their clinician.

Interventions

DIAGNOSTIC_TESTWheeze and me questionnaire

validation of questionnaire assessing disease control and quality of life in preschool children with recurrent wheeze

Sponsors

Imperial College Healthcare NHS Trust
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
2 Years to 5 Years
Healthy volunteers
Yes

Inclusion criteria

In this study caregivers of preschool children presenting with the second or more episode of wheeze that requires physician review with or without treatment (as per BTS definition of wheeze attack in preschool years) will be included.

Exclusion criteria

This study will exclude caregivers who do not consent to complete the questionnaire and therefore participate in the study. This study will exclude caregivers of preschool children who present with their first episode of wheeze. This study will exclude caregivers of preschool children who present with respiratory distress of any other etiology (foreign body inhalation, croup, lower respiratory tract infection, bronchiectasis, exacerbation of cystic fibrosis or ciliopathy)

Design outcomes

Primary

MeasureTime frameDescription
feasibility of preschool wheeze assessment toolMarch 2019 - March 2020how easily the questionnaire can be completed
content validity of the questionnaireMarch 2019-March 2020assessing validity of each item of the questionnaire as comparing with item of already existing questionnaire

Secondary

MeasureTime frameDescription
reduction of avoidable emergency department admissionsMarch 2020-March 2021effect of the tool on number of avoidable emergency department presentations

Countries

United Kingdom

Contacts

Primary ContactHeidi Makrinioti
heidimakrinioti@gmail.com07771348633

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026