Can a new questionnaire capture how bronchiectasis affects Children's daily lives?
NCT ID NCT07728006
First seen Jul 27, 2026 · Last updated Jul 28, 2026 · Updated 1 time
Summary
This study aims to create a disease-specific quality-of-life questionnaire for children with bronchiectasis, a chronic lung condition. Researchers will interview children, teenagers, and parents to understand the key impacts of the disease. The final questionnaire will be tailored for different age groups and parent-proxy versions, helping clinicians better assess and address patients' needs.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could give doctors a better tool to measure how bronchiectasis affects children's daily lives, helping tailor care.
- What could go wrong
- This is an early-stage questionnaire development study, not a treatment trial. The questionnaire may need further validation before widespread use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 78 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients aged 2years to 17 years with a CT diagnosis of Paediatric Bronchiectasis -unrelated to CF or PCD. Also parents of children and young people aged 2years-12years with a CT diagnosis of Paediatric Bronchiectasis -unrelated to CF or PCD.
- Ages
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2 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient, child and young persons, aged 8 -17 years with bronchiectasis diagnosed on CT scan * Parent of child aged 2-12 years with bronchiectasis diagnosed on CT scan * Written informed consent/assent available Exclusion Criteria: * Child under 8 years with bronchiectasis for patient direct participation * No consent/assent received * Confirmed Cystic Fibrosis or Primary Ciliary Dyskinesia diagnosis
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Birmingham Womens and Childrens NHS Foundation Trust
Birmingham, B4 6NH, United Kingdom