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Pollution Intervention to Impact Kids Asthma Study

Recruiting

Who can join

Ages 8 to 17 · All sexes

Full eligibility criteria
Inclusion Criteria:

* A healthcare provider diagnosis of persistent asthma (Steps 2-5 as defined by US guidelines) or intermittent asthma (Step 1) + at least one severe asthma exacerbation (defined by American Thoracic Society (ATS)/European Respiratory Society (ERS) criteria as requiring at least 3 days of systemic steroids or an Emergency Department/Urgent Care visit requiring systemic steroids) in the prior 12 months
* Home access to a smartphone or internet
* Primary residence in Allegheny County, PA
* One participant per household
* Age 8 -17 years
* Healthcare provider evaluation for asthma in the prior year

Exclusion Criteria:

* Diagnosis of other active chronic respiratory diseases (e.g., cystic fibrosis, bronchopulmonary dysplasia, etc.)
* Neuromuscular disorder
* Chronic disorder limiting independent ambulation (e.g., spastic quadriplegia, etc.)
* Cyanotic heart disease
* Plans to relocate from Allegheny County, PA in the next year (12 months)
* Use of intranasal or oral/intramuscular/intravenous corticosteroids 4 weeks prior to randomization
* Current participation in another asthma intervention trial

About the study

The goal of this clinical trial is to learn if adding Air Quality Index (AQI) information to asthma action plans works to improve asthma outcomes in children. It will also learn about children with asthma who report being more sensitive to outdoor air pollution. The main questions it aims to answer are:

* Does adding either information about the EPA-AQI or commercial AQI improve asthma outcomes over time? * Are there changes in nasal gene expression in children with asthma who report they are more sensitive to outdoor air pollution?

Researchers will compare EPA-AQI and the commercial-AQI groups to a control group to either AQI works to improve asthma.

Participants will:

* Receive standardized outdoor air pollution education and an asthma action plan * Provide nose and blood specimens * Have visits every 4 weeks for 48 weeks, 10 will be conducted by telephone calls and 3 visits will be in person.

What is being tested

Sponsor: University of Pittsburgh · Participants: 351 · Started: Feb 24, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07261423

Locations in the U.S.

PennsylvaniaUPMC Children's Hospital of Pittsburgh, Pittsburgh

From ClinicalTrials.gov, data retrieved Oct 1, 2026. Each study sets its own eligibility; the study team decides who can join.