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哮喘高危青少年的体内黏附干预:一项随机试验的报告。

The in vivo adherence intervention for at risk adolescents with asthma: report of a randomized pilot trial.

机构信息

Division of Pulmonary Medicine, Cincinnati Children’s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

出版信息

J Pediatr Psychol. 2012 May;37(4):390-403. doi: 10.1093/jpepsy/jsr107. Epub 2011 Dec 13.

Abstract

OBJECTIVE

Low-income and minority adolescents are at high risk for poor asthma outcomes, due in part to adherence. We tested acceptability, feasibility, and effect sizes of an adherence intervention for low socioeconomic status (SES) minority youth with moderate- and severe-persistent asthma. Design and Methods Single-site randomized pilot trial: intervention (n = 12; asthma education, motivational interviewing, problem-solving skills training, 1 month cell-phone with tailored text messaging) versus control (n = 14; asthma education; cell-phone without tailored messaging). Calculated effect-sizes of relative change from baseline (1 and 3 months).

RESULTS

Intervention was judged acceptable and feasible by participants. Participants (12-18 years, mean = 15.1, SD = 1.67) were 76.9% African-American, 80.7% public/no insurance. At 1 and 3 months, asthma symptoms (Cohen's d's = 0.40, 0.96) and HRQOL (PedsQL™; Cohen's d's = 0.23, 1.25) had clinically meaningful medium to large effect sizes.

CONCLUSIONS

This intervention appears promising for at-risk youth with moderate- and severe-persistent asthma.

摘要

目的

由于依从性等原因,低收入和少数族裔青少年罹患哮喘后预后较差的风险较高。我们测试了一种针对中重度持续性哮喘的低收入少数族裔青少年的依从性干预措施的可接受性、可行性和效果大小。

设计和方法

单站点随机试点试验:干预组(n=12;哮喘教育、动机访谈、解决问题技能培训、1 个月带个性化短信的手机)与对照组(n=14;哮喘教育;不带个性化短信的手机)。从基线(1 个月和 3 个月)计算相对变化的效应大小。

结果

参与者认为干预措施是可以接受和可行的。参与者(12-18 岁,平均=15.1,SD=1.67)中 76.9%为非裔美国人,80.7%为公共/无保险。在 1 个月和 3 个月时,哮喘症状(Cohen's d's=0.40, 0.96)和 HRQOL(PedsQL™;Cohen's d's=0.23, 1.25)具有临床意义的中到大效应大小。

结论

对于中重度持续性哮喘的高危青少年,这种干预措施似乎很有前景。

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