Using Mobile Phones to Improve Adherence to Inhaled Steroids
- Conditions
- Asthma
- Interventions
- Behavioral: Asthma SupervisionBehavioral: Mobile PhoneBehavioral: Inhaled Corticosteroid Mobile Phone ApplicationBehavioral: 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
- 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
- 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
Group Intervention Description Experimental: Intervention Group Inhaled Corticosteroid Mobile Phone Application Experimental: 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 Group Beta2-adrenergic agonist Mobile Phone Application Experimental: 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 Group Asthma Supervision Experimental: 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 Group Mobile Phone Experimental: 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
Name Time Method Adherence to inhaled corticosteroids, measured objectively using an electronic dose counter 10 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
Name Time Method To understand patterns of use of quick-relief medication for asthma 10 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