首页> 外文OA文献 >A pragmatic randomised controlled trial assessing the non-inferiority of counselling for depression versus cognitive-behaviour therapy for patients in primary care meeting a diagnosis of moderate or severe depression (PRaCTICED): Study protocol for a randomised controlled trial.
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A pragmatic randomised controlled trial assessing the non-inferiority of counselling for depression versus cognitive-behaviour therapy for patients in primary care meeting a diagnosis of moderate or severe depression (PRaCTICED): Study protocol for a randomised controlled trial.

机译:一项实用的随机对照试验,评估针对中度或重度抑郁症诊断的初级保健患者的抑郁症与认知行为治疗咨询的非劣效性(pRaCTICED):随机对照试验的研究方案。

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摘要

BACKGROUND: NICE guidelines state cognitive behavioural therapy (CBT) is a front-line psychological treatment for people presenting with depression in primary care. Counselling for Depression (CfD), a form of Person-Centred Experiential therapy, is also offered within Improving Access to Psychological Therapies (IAPT) services for moderate depression but its effectiveness for severe depression has not been investigated. A full-scale randomised controlled trial to determine the efficacy and cost-effectiveness of CfD is required. METHODS: PRaCTICED is a two-arm, parallel group, non-inferiority randomised controlled trial comparing CfD against CBT. It is embedded within the local IAPT service using a stepped care service delivery model where CBT and CfD are routinely offered at step 3. Trial inclusion criteria comprise patients aged 18 years or over, wishing to work on their depression, judged to require a step 3 intervention, and meeting an ICD-10 diagnosis of moderate or severe depression. Patients are randomised using a centralised, web-based system to CfD or CBT with each treatment being delivered up to a maximum 20 sessions. Both interventions are manualised with treatment fidelity tested via supervision and random sampling of sessions using adherence/competency scales. The primary outcome measure is the Patient Health Questionnaire-9 collected at baseline, 6 and 12 months. Secondary outcome measures tap depression, generic psychological distress, anxiety, functioning and quality of life. Cost-effectiveness is determined by a patient service receipt questionnaire. Exit interviews are conducted with patients by research assessors blind to treatment allocation. The trial requires 500 patients (250 per arm) to test the non-inferiority hypothesis of -2 PHQ-9 points at the one-sided, 2.5% significance level with 90% power, assuming no underlying difference and a standard deviation of 6.9. The primary analysis will be undertaken on all patients randomised (intent to treat) alongside per-protocol and complier-average causal effect analyses as recommended by the extension to the CONSORT statement for non-inferiority trials. DISCUSSION: This large-scale trial utilises routinely collected outcome data as well as specific trial data to provide evidence of the comparative efficacy and cost-effectiveness of Counselling for Depression compared with Cognitive Behaviour Therapy as delivered within the UK government's Improving Access to Psychological Therapies initiative. TRIAL REGISTRATION: Controlled Trials ISRCTN Registry, ISRCTN06461651 . Registered on 14 September 2014.
机译:背景:NICE指南指出,认知行为疗法(CBT)是针对初级保健中出现抑郁症的人的一线心理治疗。心理咨询服务(CfD)是一种以人为中心的体验式治疗形式,还为改善中度抑郁症的心理治疗(IAPT)服务提供,但尚未研究其对严重抑郁症的有效性。需要一项全面的随机对照试验来确定CfD的疗效和成本效益。方法:PRACTICED是一个两臂平行组的​​非劣效性随机对照试验,比较了CfD和CBT。它使用分步式护理服务提供模式嵌入本地IAPT服务中,其中在步骤3常规提供CBT和CfD。试验纳入标准包括18岁或18岁以上,希望接受抑郁治疗的患者,被认为需要进行步骤3干预,并达到中度或重度抑郁的ICD-10诊断。使用基于网络的集中式系统将患者随机分为CfD或CBT,每次治疗最多可进行20次治疗。两种干预都是通过对治疗的保真度进行手动操作来实现的,这些保真度通过依从性/能力量表的监督和随机抽样来进行。主要结局指标是在基线,6和12个月收集的《患者健康问卷9》。次要结局指标包括轻拍抑郁,一般性心理困扰,焦虑,功能和生活质量。成本效益由患者服务收据调查表确定。退出访谈由对治疗分配不知情的研究评估人员对患者进行。该试验要求500名患者(每臂250名)在单侧,2.5%显着性水平和90%功效下测试-2 PHQ-9点的非劣效性假设,假设无根本差异且标准差为6.9。将对CONSORT声明扩展至非劣效性试验的所有患者(根据治疗方案)以及按方案和符合标准者的因果效应分析进行初步分析。讨论:这项大规模试验利用常规收集的结局数据和特定试验数据来提供证据,证明在英国政府的“改善获得心理疗法的机会”计划中,与认知行为疗法相比,抑郁症咨询的相对功效和成本效益。 。试用注册:对照试验ISRCTN注册中心,ISRCTN06461651。 2014年9月14日注册。

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