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首页> 外文期刊>BMC Psychiatry >REFOCUS Trial: protocol for a cluster randomised controlled trial of a pro-recovery intervention within community based mental health teams
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REFOCUS Trial: protocol for a cluster randomised controlled trial of a pro-recovery intervention within community based mental health teams

机译:REFOCUS试验:基于社区的精神卫生小组中的康复康复干预措施的集群随机对照试验方案

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Background There is a consensus about the importance of 'recovery' in mental health services, but the evidence base is limited. Methods/Design A two centre, cluster randomised controlled trial. Participants are community-based mental health teams, and service users aged 18-65 years with a primary clinical diagnosis of psychosis. In relation to the REFOCUS Manual researchintorecovery.com/refocus, which describes a 12-month, pro-recovery intervention based on the REFOCUS Model, the objectives are: (1) To establish the effectiveness of the intervention described in the REFOCUS Manual; (2) To validate the REFOCUS Model; (3) To establish and optimise trial parameters for the REFOCUS Manual; and (4) To understand the relationship between clinical outcomes and recovery outcomes. The hypothesis for the main study is that service users in the intervention arm will experience significantly greater increases in measures of personal recovery (as measured by the QPR) compared to service users receiving care from control teams. The hypothesis for the secondary study is that black service users in the intervention arm will experience significantly greater increases in measures of personal recovery (as measured by the QPR) and client satisfaction (as measured by the CSQ) compared to Black service users receiving care from control teams. The intervention comprises treatment as usual plus two components: recovery-promoting relationships and working practices. The control condition is treatment as usual. The primary outcme is the Process of Recovery Questionnaire (QPR). Secondary outcomes are satisfaction, Goal setting - Personal Primary Outcome, hope, well-being, empowerment, and quality of life. Primary outcomes for the secondary study will be QPR and satisfaction. Cost data will be estimated, and clinical outcomes will also be reported (symptomatology, need, social disability, functioning). 29 teams (15 intervention and 14 control) will be randomised. Within each team, 15 services users will be randomly chosen, giving a total sample of 435 service users (225 in intervention and 210 in control). Power for the main study: 336 service users will give power to detect a medium effect size of 0.4 (alpha 0.05, power = 0.8) on both QPR sub-scales. Power for the secondary study: 89 participants will give power to detect an effect size of 0.67 on both QPR sub-scales and on CSQ. A range of approaches are used to minimise bias, although service users and clinicians cannot be blinded. Discussion This cluster-RCT will evaluate a pro-recovery intervention in community mental health teams. Trial registration ISRCTN: ISRCTN02507940
机译:背景技术关于“康复”在精神卫生服务中的重要性存在共识,但证据基础有限。方法/设计一项两中心,集群的随机对照试验。参加者是基于社区的精神卫生小组,其服务使用者年龄在18-65岁之间,主要诊断为精神病。关于REFOCUS手册researchintorecovery.com/refocus,它描述了基于REFOCUS模型的为期12个月的恢复前干预措施,其目标是:(1)确定REFOCUS手册中所述干预措施的有效性; (2)验证REFOCUS模型; (3)为REFOCUS手册建立和优化试验参数; (4)了解临床预后与恢复预后之间的关系。这项主要研究的假设是,与从控制小组接受护理的服务使用者相比,干预部门的服务使用者的人身康复量(通过QPR衡量)将显着增加。次级研究的假设是,与接受以下服务的黑人服务使用者相比,干预部门中的黑人服务使用者在个人康复(通过QPR衡量)和客户满意度(通过CSQ衡量)方面将经历更大的增长。控制团队。干预措施包括照常治疗以及两个组成部分:促进恢复的关系和工作习惯。控制条件是照常治疗。主要结果是恢复问卷调查流程(QPR)。次要结果是满意度,目标设定-个人主要结果,希望,幸福感,能力和生活质量。中学研究的主要结果将是QPR和满意度。费用数据将被估计,临床结果也将被报告(症状,需求,社会残疾,功能)。将随机分配29个小组(15个干预小组和14个对照组)。在每个团队中,将随机选择15位服务用户,从而得出435位服务用户的总样本(225位干预用户和210位对照用户)。主要研究的功效:336名服务使用者将有能力在两个QPR分量表上检测到0.4的中等效应大小(alpha 0.05,功效= 0.8)。二次研究的功效:89名参与者将有权在QPR分量表和CSQ上检测到0.67的效应量。尽管服务使用者和临床医生不能盲目,但仍采用了多种方法来最大程度地减少偏差。讨论该CRT-RCT将评估社区精神卫生小组的康复干预措施。试用注册ISRCTN:ISRCTN02507940

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