McKinney Walker S, Tadevich Lauren J, Schmitt Lauren M, Horn Paul S, Ruberg Jennnifer R, White Susan W, Reisinger Debra L, Burkett Karen W, Sarawgi Shivali, Kang Sungeun, Shaffer Rebecca C
Department of Behavioral Medicine and Clinical Psychology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
BMC Psychol. 2025 Apr 24;13(1):436. doi: 10.1186/s40359-025-02737-6.
Emotion dysregulation is a common concern in autistic youth. Growing evidence suggests emotion dysregulation underlies multiple co-occurring issues in autism, including externalizing (e.g., aggression, irritability) and internalizing (e.g., anxiety, depression) disorders, and thus may serve as a key transdiagnostic treatment target. Emotion dysregulation during middle childhood (8-12 years) is concurrently and longitudinally associated with social difficulties and poorer quality of life for autistic individuals, highlighting a key window for intervention. There is an urgent need for treatments for emotion dysregulation in school-age autistic youth that involve caregivers to maximize skill generalization. To address this need, our group developed Regulating Together, an intensive outpatient group program targeting emotion dysregulation in 8- to 12-year-old autistic youth that integrates strategies from cognitive behavioral therapy, mindfulness and acceptance-based therapies, and parent training programs. Building on our previous non-randomized trials of Regulating Together, we document the study protocol for our first, and ongoing, randomized controlled trial comparing Regulating Together to an active control condition.
This is a five-year randomized controlled trial comparing Regulating Together to Achieving Independence and Mastery in School (AIMS), an active control condition targeting executive functioning difficulties, in an outpatient hospital setting. Enrollment is ongoing and the study is expected to be completed in late Fall of 2026. Participants will be 144 autistic youth (8-12 years; IQ ≥ 65) randomized to either 5-week treatment condition. A comprehensive assessment battery integrating self-, caregiver-, and clinician-report information, functional outcomes (i.e., number of psychiatric hospitalizations), objective outcomes (probabilistic reversal learning task), and biobehavioral measures (heart rate variability) will be collected and compared between baseline (Week 0), post-treatment (Week 7), post-generalization (Week 16), and at long-term follow-up (Week 29).
This is the first comparison of the Regulating Together program to an active treatment condition. Findings from this study will build on previous piloted iterations of Regulating Together by characterizing its efficacy in relation to active treatment, testing moderators of treatment response, and identifying barriers and facilitators to treatment access, impact, and sustainability. Following completion of this study, we will pursue implementation studies (e.g., testing program implementation and effectiveness in community settings). Dissemination and external provider training efforts are ongoing.
Trial registration took place through ClinicalTrials.gov (NCT05803369) on March 14th, 2023.
情绪调节障碍是自闭症青少年中常见的问题。越来越多的证据表明,情绪调节障碍是自闭症中多种并发问题的基础,包括外化问题(如攻击行为、易怒)和内化问题(如焦虑、抑郁),因此可能是一个关键的跨诊断治疗靶点。童年中期(8至12岁)的情绪调节障碍与自闭症个体的社交困难和较差的生活质量同时存在并呈纵向关联,凸显了干预的关键窗口期。迫切需要针对学龄期自闭症青少年情绪调节障碍的治疗方法,其中涉及照顾者以最大限度地提高技能泛化能力。为满足这一需求,我们团队开发了“共同调节”项目,这是一个针对8至12岁自闭症青少年情绪调节障碍的强化门诊小组项目,整合了认知行为疗法、正念和基于接纳的疗法以及家长培训项目的策略。基于我们之前对“共同调节”项目的非随机试验,我们记录了我们第一个也是正在进行的随机对照试验的研究方案,该试验将“共同调节”项目与一个积极对照条件进行比较。
这是一项为期五年的随机对照试验,在门诊医院环境中将“共同调节”项目与“在学校实现独立和掌握技能”(AIMS)进行比较,AIMS是一个针对执行功能困难的积极对照条件。招募工作正在进行,该研究预计于2026年秋末完成。参与者将是144名自闭症青少年(8至12岁;智商≥65),随机分配到两种为期5周的治疗条件之一。将收集并比较一个综合评估组套,该组套整合了自我报告、照顾者报告和临床医生报告信息、功能结局(即精神病住院次数)、客观结局(概率反转学习任务)和生物行为指标(心率变异性),比较时间点为基线(第0周)、治疗后(第7周)、泛化后(第16周)和长期随访(第29周)。
这是首次将“共同调节”项目与积极治疗条件进行比较。本研究的结果将基于之前对“共同调节”项目的试点迭代,通过描述其相对于积极治疗的疗效、测试治疗反应的调节因素以及确定治疗获取、影响和可持续性的障碍及促进因素来进行。本研究完成后,我们将开展实施研究(如测试项目在社区环境中的实施情况和有效性)。传播和外部提供者培训工作正在进行。
试验于2023年3月14日通过ClinicalTrials.gov(NCT05803369)进行注册。