MedPath

Breathing Counts: Evaluating Adherence in the Presence of Asthma Navigation Support

Not Applicable
Completed
Conditions
Asthma
Interventions
Device: Propeller Health device + asthma navigator
Registration Number
NCT03065205
Lead Sponsor
University of Colorado, Denver
Brief Summary

To determine if an asthma navigator is helpful in improving communication between care providers and improving patient adherence to asthma medications after an asthma exacerbation.

Detailed Description

This study will aim to use technology to evaluate the effectiveness of a patient navigator for childhood asthma. The Investigators will place adherence monitoring devices on patient inhalers, and track use of patient asthma medicines. The Investigators will also utilize an asthma navigator who will discuss adherence with families and help to address any barriers to adherence that families identify. Additionally, the navigator will communicate patient specific adherence information to the patient's primary care physician (PCP) and school nurse. The adherence monitor will monitor communications between these providers.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
65
Inclusion Criteria
  • Age 6-17 years old,
  • Admission to Children's Hospital Colorado with an asthma exacerbation between Jan 1 2017 and Dec 31 2017.
Exclusion Criteria
  • Language other than English or Spanish (application for monitoring adherence is only available in these languages)

  • Presence of other complex medical problems including:

    • Cystic Fibrosis,
    • Tracheostomy/ventilator dependence,
    • other severe chronic lung disease, and
    • significant developmental delays.
  • Home schooled or not in school

  • Following up with an allergy or pulmonary provider outside the CHCO system after hospital discharge.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Single ArmPropeller Health device + asthma navigatorPatients will have adherence monitoring devices placed on their asthma inhalers (both daily and rescue medication). Adherence information will be sent to their PCP, specialist and school nurse monthly. Additionally, the navigator will speak with families every 2 months to discuss adherence data and address barriers.
Primary Outcome Measures
NameTimeMethod
Change in Adherence of Use of Patient Asthma InhalersWeek 1 to Week 24

Adherence will be measured via adherence monitoring devices for 6 months per patient. Change in device measured adherence from week 1 to week 24. Measured as change in average number of puffs of controller medication taken/puffs individually prescribed, measured between weeks 1 and 24.

Secondary Outcome Measures
NameTimeMethod
Barriers to Adherence of Patient Asthma Inhalers6 months

Measured via questionnaire data obtained every 2 months. Reported at 6 months.

Effectiveness of Communication Between Providers6 months

measured via survey to providers at the end of the intervention

Degree of Asthma Control6 months

Measured via questionnaire data using Asthma Control Test (ACT) or Childhood Asthma Control Test (cACT) every 2 months. Reported at 6 months. Scores range from 5-25 on the ACT and 0-27 on the cACT. Scores \>19 on either test indicate good asthma control

Trial Locations

Locations (1)

Childrens Hospital Colorado

🇺🇸

Aurora, Colorado, United States

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