Tech tool boosts asthma care for city kids
NCT ID NCT03066596
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study tested a computer-based program that reminds doctors to follow asthma guidelines for children aged 2 to 12 with persistent or uncontrolled asthma. The program helped doctors take more corrective actions, like adjusting medication or checking triggers. The goal was to reduce asthma symptoms and improve daily life for kids in urban clinics.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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530 people
The number who actually took part.
- Started
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Mar 2017
- Finished
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Aug 2024
- 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.
- Ages
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2 to 12 years
- 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: The criteria listed below will apply to \~5,000 children from eMPI and eUC practices: * Physician-diagnosed asthma (based on EHR) * Persistent or uncontrolled asthma as per clinic assessment. Based on NHLBI guidelines, any one of the following: in past month, \> 2 days/week with asthma symptoms, \>2 days/week with rescue medication use, \>2 days/month with nighttime symptoms, or \> 2 episodes in the past year that required systemic corticosteroids * Age 2 and 12 years, inclusive Additional inclusion criteria will apply to a subset of 512 of children whose caregivers will be interviewed to obtain caregiver-reported morbidity outcomes: * Caregiver is able to speak and understand either English or Spanish. Participants unable to read will be eligible as all surveys will be administered verbally by research personnel * Consent from the primary caregiver, caregiver permission for the child to participate as well as assent from the child (\>7 years). If there are eligible siblings, only one child will be randomly selected Exclusion Criteria: * The child has other significant medical conditions, such as congenital heart disease, cystic fibrosis, or other chronic lung disease, that could interfere with the assessment of asthma-related measures Additional exclusion criteria will apply to a subset of 512 children/caregivers as described above: * No access to a telephone to conduct follow-up surveys * Children in foster care or other situations in which consent cannot be obtained from a guardian
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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.
Contacts and locations
Locations
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Children's Hospital at Montefiore, Albert Einstein College of Medicine
The Bronx, New York, 10467, United States
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Other studies related to the condition(s) this trial covers.
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