Study protocol for a pilot clinical trial to understand neural mechanisms of response to a psychological treatment for pain and anxiety in pediatric functional abdominal pain disorders (FAPD)

Natoshia R Cunningham, Michelle A Adler, Brittany N Barber Garcia, Taylor Abounader, Alaina K Miller, Mariela Monzalvo, Ismaeel Hashemi, Ryan Cox, Samantha L Ely, Yong Zhou, Mark DeLano, Todd Mulderink, Mathew J Reeves, James L Peugh, Susmita Kashikar-Zuck, Robert C Coghill, Judith E Arnetz, David C Zhu
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Abstract

Background. Functional abdominal pain disorders (FAPD) are the most common chronic pain conditions of childhood and are made worse by co-occurring anxiety. Our research team found that the Aim to Decrease Pain and Anxiety Treatment (ADAPT), a six-session coping skills program using cognitive behavioral therapy strategies, was effective in improving pain-related symptoms and anxiety symptoms compared to standard care. In follow-up, this current randomized clinical trial (RCT) aims to test potential neural mechanisms underlying the effect of ADAPT. Specifically, this two-arm RCT will explore changes in amygdalar functional connectivity (primary outcome) following the ADAPT protocol during the water loading symptom provocation task (WL-SPT). Secondary (e.g., changes in regional cerebral blood flow via pulsed arterial spin labeling MRI) and exploratory (e.g., the association between the changes in functional connectivity and clinical symptoms) outcomes will also be investigated. Methods. We will include patients ages 11 to 16 years presenting to outpatient pediatric gastroenterology care at a midwestern children’s hospital with a diagnosis of FAPD plus evidence of clinical anxiety based on a validated screening tool (the Generalized Anxiety Disorder-7 [GAD-7] measure). Eligible participants will undergo baseline neuroimaging involving the WL-SPT, and assessment of self-reported pain, anxiety, and additional symptoms, prior to being randomized to a six-week remotely delivered ADAPT program plus standard medical care or standard medical care alone (waitlist). Thereafter, subjects will complete a post assessment neuroimaging visit similar in nature to their first visit. Conclusions. This small scale RCT aims to increase understanding of potential neural mechanisms of response to ADAPT. ClinicalTrials.gov registration: NCT03518216
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了解小儿功能性腹痛(FAPD)患者对疼痛和焦虑心理治疗反应的神经机制的试点临床试验研究方案
背景。功能性腹痛症(FAPD)是儿童时期最常见的慢性疼痛疾病,并因同时伴有焦虑症而变得更加严重。我们的研究小组发现,与标准治疗相比,"旨在减轻疼痛和焦虑治疗"(ADAPT)能有效改善疼痛相关症状和焦虑症状。作为后续研究,本随机临床试验(RCT)旨在测试 ADAPT 效果的潜在神经机制。具体来说,这项双臂 RCT 将探讨在水负荷症状激发任务(WL-SPT)中使用 ADAPT 方案后杏仁核功能连接的变化(主要结果)。此外,还将研究次要结果(例如,通过脉冲动脉自旋标记核磁共振成像观察区域脑血流的变化)和探索性结果(例如,功能连通性变化与临床症状之间的关联)。我们的研究对象包括在一家中西部儿童医院小儿胃肠科门诊就诊的 11 至 16 岁患者,这些患者不仅被诊断为 FAPD,而且有证据表明他们存在临床焦虑症,这种焦虑症是基于一种经过验证的筛查工具(广泛性焦虑症-7 [GAD-7] 测量)。符合条件的受试者将接受基线神经影像学检查(包括 WL-SPT),并对自我报告的疼痛、焦虑和其他症状进行评估,然后随机接受为期六周的远程 ADAPT 计划和标准医疗护理或单独的标准医疗护理(候选名单)。此后,受试者将完成一次与首次就诊性质类似的神经影像评估后就诊。这项小规模研究旨在加深人们对ADAPT潜在神经机制的了解。ClinicalTrials.gov 注册:NCT03518216
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