Witten/Herdecke University, Witten, Germany.
Vestische Kinder- und Jugendklinik Datteln, Datteln, Germany.
BMJ Open. 2024 May 15;14(5):e083180. doi: 10.1136/bmjopen-2023-083180.
Childhood asthma is a highly prevalent chronic disease. A failure to implement patient education programmes may result in increased morbidity, despite the availability of distinct diagnostic and therapeutic approaches. Patients with lower socioeconomic status (SES) tend to have a higher asthma prevalence. Moreover, the progression of asthma is significantly influenced by factors such as health literacy and the children's specific knowledge about the condition. With this trial, the primary objective is to evaluate whether asthma education enhances specific disease understanding in children with asthma (primary outcome). Secondary objectives include evaluating training effects on health literacy, retention rates of information, 'Children Asthma Control Test' (C-ACT) score, frequency of emergency room and physician visits (secondary outcomes) and whether SES influences training effects.
To address the research objectives, this study comprises two projects. The first subproject will investigate the influence of asthma training on the development of disease understanding and health literacy. The second subproject will analyse the influence of SES on the outcome of children participating in asthma training. This research is designed as a comparative, non-randomised study involving two paediatric groups between the ages of ≥7 and < 14 years. After being diagnosed with asthma, the intervention group undergoes standardised psychoeducational asthma training at a certified centre associated with paediatricians in private practice in Germany, following the recommendations of the 'Arbeitsgruppe Asthmaschulung im Kindes- und Jugendalter e.V.', a national association aiming to establish uniform and guideline-based standards for patient education in children and adolescents. The comparison group receives a significantly shorter period of education and instruction on the usage of asthma medication at outpatient clinics. Data will be collected from patients and their parents at three specific survey time points, based on standardised tools.To describe mean differences between the intervention and control group over time (subproject 1), a repeated-measures analysis of variance (ANOVA) will be conducted. In subproject 2, multivariate linear regression analysis will be used to analyse the variables determining the changes in specific disease understanding and health literacy, including SES. The sample size calculation is based on a mixed ANOVA model with two groups and two measurements resulting in a total of 126 participants.
All protocols and a positive ethics approval were obtained from the Witten/Herdecke University, Germany (S-159, 2023; application submission: 24 June 2023, final vote: 10 July 2023). Furthermore, the study was registered at the German Clinical Trials Register (DRKS), DRKS00032423. The application submission was on 3 August 2023, and the final approval was on 4 August 2023. The results will be disseminated among experts and participants and will be published in peer-reviewed, international journal with open access.
DRKS00032423.
儿童哮喘是一种高发的慢性疾病。如果未能实施患者教育计划,尽管有明确的诊断和治疗方法,发病率仍可能上升。社会经济地位(SES)较低的患者往往哮喘发病率更高。此外,健康素养和儿童对疾病的具体了解等因素会显著影响哮喘的发展。通过这项试验,主要目的是评估哮喘教育是否能提高哮喘儿童对疾病的特定理解(主要结局)。次要目标包括评估培训对健康素养、信息保留率、“儿童哮喘控制测试”(C-ACT)评分、急诊室和医生就诊频率(次要结局)的影响,以及 SES 是否会影响培训效果。
为了实现研究目标,本研究包括两个项目。第一个子项目将研究哮喘培训对疾病理解和健康素养发展的影响。第二个子项目将分析 SES 对参与哮喘培训的儿童结果的影响。这项研究是一项比较性、非随机研究,涉及德国两家年龄在≥7 岁至<14 岁之间的儿科组。在被诊断患有哮喘后,干预组在德国的一家经认证的中心接受标准化的心理教育哮喘培训,该中心与私人执业的儿科医生有关联,并遵循“Arbeitsgruppe Asthmaschulung im Kindes- und Jugendalter e.V.”的建议,该协会旨在为儿童和青少年患者建立统一和基于指南的标准。对照组在门诊接受哮喘药物使用的教育和指导时间明显缩短。将根据标准化工具从患者及其父母处收集三个特定调查时间点的数据。为了描述干预组和对照组随时间的平均差异(子项目 1),将进行重复测量方差(ANOVA)分析。在子项目 2 中,将使用多元线性回归分析来分析确定特定疾病理解和健康素养变化的变量,包括 SES。样本量计算基于具有两组和两次测量的混合 ANOVA 模型,共 126 名参与者。
所有方案和积极的伦理批准均由德国维滕/赫德克大学获得(S-159,2023 年;申请提交:2023 年 6 月 24 日,最终投票:2023 年 7 月 10 日)。此外,该研究在德国临床试验注册处(DRKS)注册,DRKS00032423。申请提交日期为 2023 年 8 月 3 日,最终批准日期为 2023 年 8 月 4 日。结果将在专家和参与者中传播,并将在同行评议的国际开放获取期刊上发表。
DRKS00032423。