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N/A Completed N=7 Randomized Health Services Research

Interventions To Help Asthma Clinical Adherence

Asthma · Humans · Hispanic Americans · Child
Source: ClinicalTrials.gov NCT02999789 ↗
Enrolled (actual)
7
Serious AEs
0.0%
Results posted
Apr 2023
Primary outcomePrimary: Change in Percentage of Doses Received — 22.0; 12.4 Percentage of doses received

Summary

To conduct a pilot test to estimate the effect of a novel reminder system in improving daily asthma controller medication adherence rates in children with monolingual Spanish-speaking guardians who have limited English Proficiency (LEP).

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Percentage of Doses Received
22.0; 12.4
SECONDARY
Asthma Symptom Control Score Change
3.0; 0

Eligibility Criteria

Inclusion Criteria

  • The investigators will recruit 30 participants ages 5 to 17 years with a diagnosis of persistent asthma who require a daily inhaled corticosteroid metered dose inhaler and whose guardian is the person responsible for administering their daily asthma medication.
  • The investigators will recruit only participants who have received or receive care at San Francisco General Hospital's 6M Children's Health Center.
  • The investigators will recruit participants whose daily inhaled corticosteroid are metered dose inhalers (MDI) of either Flovent (fluticasone propionate) HFA (Hydrofluoroalkane) or Qvar (beclamethasone dipropionate) HFA.
  • The Investigators will recruit only participants whose guardian responsible for administering their daily asthma medication has Limited English Proficiency (LEP) and whose primary language is Spanish.

Exclusion Criteria

  • The Investigators will exclude participants whose guardian responsible for administering their daily asthma medication does not have a Bluetooth enabled cell phone capable of receiving text messages.
  • The Investigators will exclude participants whose guardian responsible for administering their daily asthma medication does not have an available reliable power outlet where they can recharge the battery of their SmartInhaler.
  • The Investigators will exclude participants whose guardian responsible for administering their daily asthma medication is unable to demonstrate correct medication technique based on standard evaluation (Press, 2011) after completion of a standard teaching protocol.
  • The Investigators will exclude participants with chronic lung disease.
  • The Investigators will exclude participants who do not have an operating system of iOS or Android on their cell phone and who have no data plan with their cellular phone plan.
  • The Investigators will exclude participants whose asthma medication regimen is being managed by an asthma subspecialist or health provider outside of the 6M Children's Health Center at San Francisco General Hospital.
  • The Investigators will exclude participants who are using an inhaled long acting beta-agonist (LABA) as part of their asthma management plan.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02999789). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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