MedPath

Using Mobile Phones to Improve Adherence to Inhaled Steroids

Not Applicable
Completed
Conditions
Asthma
Interventions
Behavioral: Asthma Supervision
Behavioral: Mobile Phone
Behavioral: Inhaled Corticosteroid Mobile Phone Application
Behavioral: Beta2-adrenergic agonist Mobile Phone Application
Registration Number
NCT01710059
Lead Sponsor
Rush University Medical Center
Brief Summary

This study has two main goals. The first goal is to test whether a mobile phone intervention can increase adherence to daily inhaled steroid medications in African American adolescents prescribed this type of medication by his/her asthma doctor. The second goal is to use a mobile phone intervention to better understand real life patterns of use of quick-relief (beta2-adrenergic agonist) asthma medication in this population.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
12
Inclusion Criteria
  • 11-16 years of age
  • self-identify as African American
  • have persistent asthma
  • be on a prescription daily inhaled corticosteroid medication for asthma
  • be on a prescription inhaled beta2-adrenergic agonist medication for asthma
Exclusion Criteria
  • candidate refusal
  • the presence of other co-morbidities that could interfere wtih study participation
  • > 60% adherence to inhaled corticosteroid medication, measured by the electronic dose counter, during the run-in period

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Experimental: Intervention GroupInhaled Corticosteroid Mobile Phone ApplicationExperimental: Intervention Group 1) Asthma Supervision; 2) Mobile Phone with talking, texting, and data plan; 3) Inhaled Corticosteroid Mobile Phone Application to provide virtual doctor supervision, immediate feedback, and positive reinforcement for taking inhaled corticosteroid medication as indicated; and 4) Beta2-adrenergic agonist Mobile Phone Application to monitor real time patterns of use of beta2-adrenergic agonist medication for asthma.
Experimental: Intervention GroupBeta2-adrenergic agonist Mobile Phone ApplicationExperimental: Intervention Group 1) Asthma Supervision; 2) Mobile Phone with talking, texting, and data plan; 3) Inhaled Corticosteroid Mobile Phone Application to provide virtual doctor supervision, immediate feedback, and positive reinforcement for taking inhaled corticosteroid medication as indicated; and 4) Beta2-adrenergic agonist Mobile Phone Application to monitor real time patterns of use of beta2-adrenergic agonist medication for asthma.
Experimental: Intervention GroupAsthma SupervisionExperimental: Intervention Group 1) Asthma Supervision; 2) Mobile Phone with talking, texting, and data plan; 3) Inhaled Corticosteroid Mobile Phone Application to provide virtual doctor supervision, immediate feedback, and positive reinforcement for taking inhaled corticosteroid medication as indicated; and 4) Beta2-adrenergic agonist Mobile Phone Application to monitor real time patterns of use of beta2-adrenergic agonist medication for asthma.
Experimental: Intervention GroupMobile PhoneExperimental: Intervention Group 1) Asthma Supervision; 2) Mobile Phone with talking, texting, and data plan; 3) Inhaled Corticosteroid Mobile Phone Application to provide virtual doctor supervision, immediate feedback, and positive reinforcement for taking inhaled corticosteroid medication as indicated; and 4) Beta2-adrenergic agonist Mobile Phone Application to monitor real time patterns of use of beta2-adrenergic agonist medication for asthma.
Primary Outcome Measures
NameTimeMethod
Adherence to inhaled corticosteroids, measured objectively using an electronic dose counter10 weeks

Adherence is measured as the mean of daily adherence to prescription inhaled corticosteroid dose over 14 days both at baseline and at week 10 of the active treatment phase. For the primary outcome, we will compare adherence at week 10 to adherence at baseline.

Secondary Outcome Measures
NameTimeMethod
To understand patterns of use of quick-relief medication for asthma10 weeks

This study will use an electronic dose counter and mobile phone technology to track participants real time use of quick-relief (beta2-adrenergic agonist) medication for asthma during the 10 weeks of active treatment.

Trial Locations

Locations (1)

Rush University Medical Center

🇺🇸

Chicago, Illinois, United States

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