Albuterol Integrated Adherence Monitoring in Children With Asthma

  • STATUS
    Recruiting
  • End date
    May 26, 2023
  • participants needed
    40
  • sponsor
    Children's Hospital Los Angeles
Updated on 26 October 2021

Summary

The investigators propose to evaluate whether an integrated electronic adherence monitoring albuterol rescue inhaler can improve proper use in a mostly minority and inner-city population of children treated for asthma at the Children's Hospital of Los Angeles

Description

This study is designed to (1) determine whether an integrated EAM albuterol rescue inhaler can increase proper use (2) determine if the monitoring capabilities of the device (flow rate, warnings) and/or increased proper use from having the device correlate with better outcomes. The investigators will also have patients perform at-home gamified spirometry (Aluna ) to (3) determine if at-home spirometry can predict albuterol use or change outcomes.

Details
Condition Asthma in Children, Childhood Asthma
Treatment Digihaler Albuterol Device by TEVA
Clinical Study IdentifierNCT04896645
SponsorChildren's Hospital Los Angeles
Last Modified on26 October 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients 8 to <19 years of age with a diagnosis of asthma as ICD-9 code 493 or ICD-10 code J45 seen in the allergy clinic at CHLA who have an albuterol rescue inhaler already prescribed and access to a personal smartphone will be eligible for recruitment

Exclusion Criteria

Patients unable to use device, unable to use albuterol (i.e. must use levalbuterol) or Age < 4 (ProAir Digihaler only approved for Subjects 4 years and older). Patients with other chronic lung disease besides asthma or other significant comorbidities that could affect lung function/asthma (e.g. significant heart defects, immunodeficiency, cystic fibrosis, etc)
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