Gerald Lynn B, McClure Leslie Ain, Harrington Kathy F, Mangan Joan M, Gibson Linda, Atchison Jody, Grad Roni
University of Alabama at Birmingham, Birmingham, AL 35249, United States.
Contemp Clin Trials. 2008 Mar;29(2):304-10. doi: 10.1016/j.cct.2007.07.010. Epub 2007 Aug 7.
Inhaled corticosteroids, when properly used, can offer considerable protection against asthma-related morbidity. However, adherence to prescribed inhaled steroids among children is low and rates differ markedly by population. The lowest rates of adherence and highest rates of morbidity are among inner-city and low income populations.
To describe the design of a school-based clinical trial in a largely minority population that is examining the efficacy of a school-based intervention intended to increase adherence to daily inhaled corticosteroids.
The supervised asthma therapy study is a two-group randomized longitudinal trial. Children were randomly assigned to either school-based supervised asthma therapy or parent supervised asthma therapy. Children were followed longitudinally for 15 months. The primary outcome of the study is the time-averaged difference between the two groups in the percentage of children experiencing at least one asthma exacerbation each month.
A web-based data collection system was designed to capture data at school. A total of 295 students, recruited from community and school sites, who attended one of 36 urban elementary schools enrolled in the study and 290 were randomized. The average age of the students was 10.0 years (sd=2.1), 91% were African American, 8% were white, and 1% were of other racial groups. 57% of students were male. The study has been recently completed and results are being analyzed.
Intervention studies requiring daily medication supervision and daily data collection can be successfully conducted within the elementary school environment.
正确使用吸入性糖皮质激素可对哮喘相关发病提供相当程度的预防作用。然而,儿童对规定的吸入性糖皮质激素的依从性较低,且不同人群的依从率差异显著。依从率最低和发病率最高的是市中心和低收入人群。
描述一项在主要为少数族裔人群中开展的基于学校的临床试验设计,该试验旨在检验一项基于学校的干预措施提高每日吸入性糖皮质激素依从性的效果。
监督性哮喘治疗研究是一项两组随机纵向试验。儿童被随机分配至基于学校的监督性哮喘治疗组或家长监督性哮喘治疗组。对儿童进行为期15个月的纵向随访。该研究的主要结局是两组中每月至少经历一次哮喘发作的儿童百分比的时间平均差异。
设计了一个基于网络的数据收集系统以在学校收集数据。从社区和学校场所招募了295名学生,这些学生就读于参与该研究的36所城市小学中的一所,其中290名被随机分组。学生的平均年龄为10.0岁(标准差=2.1),91%为非裔美国人,8%为白人,1%为其他种族群体。57%的学生为男性。该研究最近已完成,结果正在分析中。
需要每日药物监督和每日数据收集的干预研究可在小学环境中成功开展。