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A pragmatic randomized controlled trial of group transdiagnostic cognitive-behaviour therapy for anxiety disorders in primary care: study protocol

机译:初级保健中焦虑障碍组癌患者患者癌症术语的务实随机对照试验:研究方案

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Anxiety disorders are the most common mental disorders in community settings, and they are associated with significant psychological distress, functional and social impairment. While cognitive behaviour therapy (CBT) is the most consistently efficacious psychological treatment for anxiety disorders, barriers preclude widespread implementation of CBT in primary care. Transdiagnostic group CBT (tCBT) focuses on cognitive and behavioural processes and intervention strategies common to different anxiety disorders, and could be a promising alternative to conventional CBT. This study aims to examine the effectiveness of a transdiagnostic group CBT for anxiety disorders program as a complement to treatment-as-usual (TAU) in primary mental health care. The trial is a multicentre pragmatic randomized controlled trial with a pre-treatment, post-treatment, and follow-up at 4, 8 and 12-months design. Treatment and control groups. a) tCBT (12 weekly 2-h group sessions following a manualized treatment protocol); b) TAU for anxiety disorders. Inclusion criteria comprise meeting DSM-5 criteria for primary Panic Disorder, Agoraphobia, Social Anxiety Disorder and/or Generalized Anxiety Disorder. Patients are recruited in three regions in the province of Quebec, Canada. The primary outcome measures are the self-reported Beck Anxiety Inventory and the clinician-administered Anxiety and Related Disorders Interview Schedule for DSM-5 (ADIS-5); secondary outcome measures include treatment responder status based on the ADIS-5, and self-reported instruments for specific anxiety and depression symptoms, quality of life, functioning, and service utilisation. Intention-to-treat analysis. A mixed effects regression model will be used to account for between- and within-subject variations in the analysis of the longitudinal effects of the intervention. This rigorous evaluation of tCBT in the real world will provide invaluable information to decision makers, health care managers, clinicians and patients regarding the effectiveness of the intervention. Widespread implementation of tCBT protocols in primary care could lead to better effectiveness, efficiency, access and equity for the large number of patients suffering from anxiety disorders that are currently not obtaining evidence-based psychotherapy. ClinicalTrials.gov: NCT02811458 .
机译:焦虑症是社区环境中最常见的精神障碍,它们与显着的心理困扰,功能和社会障碍有关。虽然认知行为治疗(CBT)是焦虑症最为有效的心理治疗,但障碍妨碍初级保健中的CBT广泛实施。 Transdiagnostic Group CBT(TCBT)侧重于不同焦虑障碍的认知和行为过程和干预策略,并且可能是传统CBT的有希望的替代品。本研究旨在检测焦虑症CBT对焦虑症的有效性,以焦虑症计划作为对初级心理保健治疗的常规(TAU)的补充。该试验是一种多期形务实随机对照试验,其预处理,后处理和随访4,8和12个月的设计。治疗和对照组。 a)TCBT(手动治疗协议后12个每周2-H组会议); b)焦虑症陶氏。纳入标准包括满足小型恐慌症,广播恐怖症,社交焦虑症和/或广泛性焦虑症的标准。患者在加拿大魁北克省省的三个地区招募。主要成果措施是自我报告的贝克焦虑库存和临床医生焦虑和相关障碍的DSM-5(ADIS-5);次要结果措施包括基于ADIS-5的治疗响应者状态,以及用于特异性焦虑和抑郁症状,生活质量,运作和服务利用的自我报告的仪器。意向治疗分析。混合效应回归模型将用于解释在分析干预的纵向效应的纵向效应之间的和课程内的变化之间。对现实世界中TCBT的严格评估将为决策者,医疗管理人员,临床医生和患者提供有关干预的有效性的宝贵信息。在初级保健方面的大规模议定书的广泛实施可能导致大量患有目前未获得基于证据的心理治疗的焦虑症的大量患者的有效性,效率,获取和权益。 ClinicalTrials.gov:NCT02811458。

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