Wagner Janelle L, Patel Anup D, Huszti Heather, Schmidt Matthew, Smith Gigi, Bhatia Sonal, Guilfoyle Shanna M, Lang Amy, Buschhaus Stacy, Williams Shannon, Ardo Jessica, Davidian Marie, Modi Avani C
College of Nursing, Medical University of South Carolina, Charleston, SC, USA.
Division of Neurology, Nationwide Children's Hospital, Columbus, OH, USA.
Contemp Clin Trials. 2024 Dec;147:107739. doi: 10.1016/j.cct.2024.107739. Epub 2024 Nov 10.
Epilepsy is a common, chronic pediatric neurological condition predominately treated with anti-seizure medications (ASMs) to control or reduce seizures. Approximately 60 % of youth with epilepsy demonstrate suboptimal adherence to their ASM. This paper describes the methodology, recruitment, design, and baseline participant characteristics of a sequential, multiple assignment, randomized trial (SMART) designed to test the effectiveness of a behavioral health intervention to improve adherence in families of young children with epilepsy.
Using a two-stage SMART, youth ages 2-12 years old with newly diagnosed epilepsy and their families were enrolled. Following an 8-week run-in phase, families with ≤95 % adherence were randomized to control (education + automated digital reminders) or intervention (education + automated digital reminders + individualized feedback) arms. After three months, families in the intervention group who remained non-adherent (i.e., ≤ 95 %) were re-randomized to 1) continue with same intervention or 2) receive two telehealth problem-solving sessions with an interventionist over the next two months. Study measures were completed at baseline, 8-, 14-, and 20-months post-baseline.
Of the n = 466 ethnically and racially diverse study participants, n = 268 participants were non-adherent and were randomized. The primary outcome was electronically monitored ASM adherence at post-intervention, while secondary outcomes included seizure freedom, health care utilization, and epilepsy-specific health-related quality of life.
Novel aspects of the trial design (e.g., sequential, recruitment of racial and ethnic diverse youth), modifications to the protocol related to the COVID-19 pandemic and evolving socio-political and medical climate, as well as recruitment and retention challenges are discussed.
gov Number: NCT03817229.
癫痫是一种常见的儿童慢性神经系统疾病,主要通过抗癫痫药物(ASMs)来控制或减少癫痫发作。约60%的癫痫青少年对其抗癫痫药物的依从性欠佳。本文描述了一项序贯、多重分配随机试验(SMART)的方法、招募、设计及基线参与者特征,该试验旨在测试一种行为健康干预措施对提高癫痫幼儿家庭依从性的有效性。
采用两阶段SMART,招募2至12岁新诊断为癫痫的青少年及其家庭。在为期8周的导入期后,依从性≤95%的家庭被随机分为对照组(教育+自动数字提醒)或干预组(教育+自动数字提醒+个性化反馈)。三个月后,干预组中仍不依从(即≤95%)的家庭被再次随机分为:1)继续接受相同干预;2)在接下来的两个月里接受两次由干预专家进行的远程医疗问题解决会议。研究指标在基线、基线后8个月、14个月和20个月时完成。
在n = 466名种族和民族多样化的研究参与者中,n = 268名参与者不依从并被随机分组。主要结局是干预后通过电子监测的抗癫痫药物依从性,次要结局包括无癫痫发作、医疗保健利用情况以及癫痫特异性健康相关生活质量。
讨论了试验设计的新颖之处(如序贯、招募种族和民族多样化的青少年)、与COVID-19大流行以及不断变化的社会政治和医疗环境相关的方案修改,以及招募和保留方面的挑战。
gov编号:NCT03817229。