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自闭症成人抑郁自助引导的有效性和成本效益:自闭症抑郁试验(ADEPT-2)-一项远程提供低强度干预的多中心随机对照试验方案。

Effectiveness and cost-effectiveness of guided self-help for depression for autistic adults: the Autism Depression Trial (ADEPT-2) - protocol for a multicentre, randomised controlled trial of a remotely delivered low-intensity intervention.

机构信息

Bristol Trials Centre, University of Bristol, Bristol, UK.

Cardiff and Vale Integrated Autism Services, Cardiff and Vale University Health Board, Cardiff, UK.

出版信息

BMJ Open. 2024 Nov 19;14(11):e084729. doi: 10.1136/bmjopen-2024-084729.

Abstract

INTRODUCTION

Depression is three to four times more prevalent in autistic people and is related to reduced quality of life. There is a need for empirically supported psychological interventions for depression specifically adapted to meet the needs of autistic adults. ADEPT-2 aims to establish the clinical and cost-effectiveness of an adapted low-intensity psychological intervention (guided self-help) for depression in autistic adults.

METHODS AND ANALYSIS

A two parallel-group multicentre pragmatic randomised controlled trial investigating the effectiveness of GSH for depression in autistic adults. Participants (n=248) aged ≥18 years with a clinical diagnosis of autism currently experiencing depression will be randomised to GSH or treatment as usual (TAU). GSH is a low-intensity psychological intervention based on the principles of behavioural activation adapted for autism. GSH comprises informational materials for nine individual sessions facilitated online by a GSH coach who has received training and supervision in delivering the intervention. The primary outcome will be Beck Depression Inventory-II depression scores at 16 weeks post randomisation with follow-up measures at 32 and 52 weeks. Additional measures of anxiety, patient-rated global improvement, quality of life, work and social adjustment, positive and negative affect will be measured 16 and 52 weeks post randomisation. The primary health economic analysis will assess the cost-effectiveness of GSH compared with TAU over 52 weeks, from a societal perspective including the National Health Service, personal social services, personal expenses, voluntary services and productivity. An embedded qualitative study will explore the acceptability, experiences and adherence of participants and therapists to treatment principles.

ETHICS AND DISSEMINATION

This trial has been approved by the East of England - Essex Research Ethics Committee on 10 June 2022 (REC Reference number: 22/EE/0091). The findings of the research will be submitted for publication in peer-reviewed journals and disseminated in an appropriate format to trial participants and the wider public.

TRIAL REGISTRATION NUMBER

ISRCTN17547011.

摘要

简介

自闭症患者的抑郁症患病率是普通人群的三到四倍,且与生活质量下降有关。需要针对自闭症成人的具体需求,开发经实证支持的专门用于治疗抑郁症的心理干预措施。ADEPT-2 旨在确定针对自闭症成人的改良型低强度心理干预(指导性自助)治疗抑郁症的临床疗效和成本效益。

方法和分析

这是一项在自闭症成人中比较指导性自助治疗与常规治疗(TAU)对抑郁症疗效的 2 组平行组、多中心实用随机对照试验。纳入年龄≥18 岁、经临床诊断为自闭症、目前正在经历抑郁症的参与者,将其随机分配至接受指导性自助治疗或 TAU。指导性自助是一种基于行为激活原理、针对自闭症患者进行改良的低强度心理干预。该干预包含 9 次个体辅导的信息资料,由接受过培训和督导的指导性自助教练在线提供。主要结局指标为随机分组后 16 周时贝克抑郁量表 II(BDI-II)评分,随访时间点为 32 周和 52 周。次要结局指标包括焦虑、患者自评总体改善、生活质量、工作和社会适应、正性和负性情绪,分别于随机分组后 16 周和 52 周进行评估。主要健康经济学分析将从社会角度(包括国家医疗服务体系、个人社会服务、个人支出、志愿服务和生产力)评估 52 周时指导性自助治疗与 TAU 的成本效益。一项嵌入式定性研究将探索参与者和治疗师对治疗原则的接受度、体验和依从性。

伦理和推广

该试验于 2022 年 6 月 10 日获得东英格兰埃塞克斯研究伦理委员会的批准(REC 参考编号:22/EE/0091)。研究结果将提交给同行评议期刊发表,并以适当的格式传播给试验参与者和更广泛的公众。

试验注册号

ISRCTN82316164。

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