Population Health Sciences, University of Bristol, Bristol, UK.
NIHR Bristol Biomedical Research Centre, Bristol, UK.
Trials. 2024 Jan 11;25(1):37. doi: 10.1186/s13063-023-07847-3.
Selective serotonin reuptake inhibitors (SSRIs) are commonly prescribed to manage anxiety in adults with an autism diagnosis. However, their effectiveness and adverse effect profile in the autistic population are not well known. This trial aims to determine the effectiveness and cost-effectiveness of the SSRI sertraline in reducing symptoms of anxiety and improving quality of life in adults with a diagnosis of autism compared with placebo and to quantify any adverse effects.
STRATA is a two-parallel group, multi-centre, pragmatic, double-blind, randomised placebo-controlled trial with allocation at the level of the individual. It will be delivered through recruiting sites with autism services in 4 regional centres in the United Kingdom (UK) and 1 in Australia. Adults with an autism diagnosis and a Generalised Anxiety Disorder Assessment (GAD-7) score ≥ 10 at screening will be randomised 1:1 to either 25 mg sertraline or placebo, with subsequent flexible dose titration up to 200 mg. The primary outcome is GAD-7 scores at 16 weeks post-randomisation. Secondary outcomes include adverse effects, proportionate change in GAD-7 scores including 50% reduction, social anxiety, obsessive-compulsive symptoms, panic attacks, repetitive behaviours, meltdowns, depressive symptoms, composite depression and anxiety, functioning and disability and quality of life. Carer burden will be assessed in a linked carer sub-study. Outcome data will be collected using online/paper methods via video call, face-to-face or telephone according to participant preference at 16, 24 and 52 weeks post-randomisation, with brief safety checks and data collection at 1-2, 4, 8, 12 and 36 weeks. An economic evaluation to study the cost-effectiveness of sertraline vs placebo and a QuinteT Recruitment Intervention (QRI) to optimise recruitment and informed consent are embedded within the trial. Qualitative interviews at various times during the study will explore experiences of participating and taking the trial medication.
Results from this study should help autistic adults and their clinicians make evidence-based decisions on the use of sertraline for managing anxiety in this population.
ISRCTN, ISRCTN15984604 . Registered on 08 February 2021. EudraCT 2019-004312-66. ANZCTR ACTRN12621000801819. Registered on 07 April 2021.
选择性 5-羟色胺再摄取抑制剂(SSRIs)常用于治疗成人自闭症患者的焦虑症。然而,其在自闭症人群中的有效性和不良影响尚不清楚。本试验旨在确定 SSRI 舍曲林在降低自闭症成人焦虑症状和改善生活质量方面的有效性和成本效益,与安慰剂相比,并量化任何不良反应。
STRATA 是一项两平行组、多中心、实用、双盲、随机、安慰剂对照试验,个体水平进行分组。它将通过英国(UK)4 个区域中心和澳大利亚的 1 个自闭症服务招募点进行,这些招募点将招募筛选时广泛性焦虑症评估(GAD-7)评分≥10 的自闭症诊断成人患者。患者将被随机分配到 25mg 舍曲林或安慰剂组,1:1 分配,随后进行灵活剂量滴定至 200mg。主要结局是随机分组后 16 周的 GAD-7 评分。次要结局包括不良反应、GAD-7 评分的比例变化(包括 50%的降低)、社交焦虑、强迫症状、惊恐发作、重复行为、情绪崩溃、抑郁症状、抑郁和焦虑综合症状、功能和残疾以及生活质量。在一个相关的护理者子研究中评估护理者负担。使用在线/纸质方法,通过视频通话、面对面或电话根据参与者的偏好,在随机分组后 16、24 和 52 周收集结局数据,并在 1-2、4、8、12 和 36 周进行简短的安全性检查和数据收集。一项经济评估研究了舍曲林与安慰剂的成本效益,一项 QuinteT 招募干预(QRI)优化了招募和知情同意,该研究嵌入在试验中。在研究过程中的不同时间进行定性访谈,以探讨参与和服用试验药物的经验。
本研究的结果应有助于自闭症成人及其临床医生在该人群中管理焦虑时做出基于证据的决策。
ISRCTN,ISRCTN86325518。2021 年 2 月 8 日注册。EudraCT 2019-004312-66。ANZCTR ACTRN12621000801819。2021 年 4 月 7 日注册。