Trial Manager, Institute of Mental Health, University of Nottingham, Nottingham, UK.
Research Fellow and Trial Therapist, NIHR MindTech Medtech Co-operative, Institute of Mental Health, University of Nottingham, Nottingham, UK.
BMJ Open. 2019 Jan 3;9(1):e027583. doi: 10.1136/bmjopen-2018-027583.
Tourette syndrome and chronic tic disorder are common, disabling childhood-onset conditions. Guidelines recommend that behavioural therapy should be offered as first-line treatment for children with tics. However, there are very few trained behaviour therapists for tics and many patients cannot access appropriate care. This trial investigates whether an internet-delivered intervention for tics can reduce severity of symptoms.
This parallel-group, single-blind, randomised controlled superiority trial with an internal pilot will recruit children and young people (aged 9-17 years) with tic disorders. Participants will be randomised to receive 10 weeks of either online, remotely delivered, therapist-supported exposure response prevention behavioural therapy for tics, or online, remotely delivered, therapist-supported education about tics and co-occurring conditions. Participants will be followed up mid-treatment, and 3, 6, 12 and 18 months post randomisation.The primary outcome is reduction in tic severity as measured on the Yale Global Tic Severity Scale total tic severity score. Secondary outcomes include a cost-effectiveness analysis and estimate of the longer-term impact on patient outcomes and healthcare services. An integrated process evaluation will analyse quantitative and qualitative data in order to fully explore the implementation of the intervention and identify barriers and facilitators to implementation. The trial is funded by the National Institute of Health Research (NIHR), Health Technology Assessment (16/19/02).
The findings from the study will inform clinicians, healthcare providers and policy makers about the clinical and cost-effectiveness of an internet delivered treatment for children and young people with tics. The results will be submitted for publication in peer-reviewed journals. The study has received ethical approval from North West Greater Manchester Research Ethics Committee (ref.: 18/NW/0079).
ISRCTN70758207 and NCT03483493; Pre-results.
妥瑞氏症候群和慢性抽动障碍是常见的儿童发病、致残性疾病。指南建议将行为疗法作为治疗抽动儿童的一线治疗方法。然而,能够治疗抽动的训练有素的行为治疗师非常少,许多患者无法获得适当的护理。本试验旨在研究互联网为基础的抽动干预是否可以减轻症状的严重程度。
这是一项平行组、单盲、随机对照优势试验,设有内部试验。试验将招募患有抽动障碍的儿童和青少年(9-17 岁)。参与者将被随机分配接受 10 周的在线、远程提供、治疗师支持的暴露反应预防行为疗法治疗抽动,或在线、远程提供、治疗师支持的抽动和共病状况的教育。参与者将在治疗中期、3、6、12 和 18 个月时进行随访。主要结局是用耶鲁总体抽动严重程度量表(Yale Global Tic Severity Scale)的总抽动严重程度评分衡量的抽动严重程度的降低。次要结局包括成本效益分析和对患者结局和医疗保健服务的长期影响的估计。综合过程评估将分析定量和定性数据,以充分探索干预措施的实施情况,并确定实施的障碍和促进因素。该试验由英国国家卫生研究院(NIHR)、卫生技术评估(16/19/02)资助。
该研究的结果将为临床医生、医疗保健提供者和决策者提供有关互联网为基础的儿童和青少年抽动治疗的临床和成本效益的信息。研究结果将提交给同行评议期刊发表。该研究已获得西北大曼彻斯特研究伦理委员会的伦理批准(参考号:18/NW/0079)。
ISRCTN70758207 和 NCT03483493;预结果。