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临床试验/NCT01710059
NCT01710059已完成不适用

Refined ADEPT: Human Augmentics for Sustained Wellbeing

Rush University Medical Center2 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2012年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
12
试验地点
2
主要终点
Adherence to inhaled corticosteroids, measured objectively using an electronic dose counter

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
11 Years 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

Adherence to inhaled corticosteroids, measured objectively using an electronic dose counter

时间窗: 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.

次要结局

  • To understand patterns of use of quick-relief medication for asthma(10 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Giselle Mosnaim

Principal Investigator

Rush University Medical Center

研究点 (2)

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