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A randomised controlled trial of hearing and vision support in dementia: Protocol for a process evaluation in the SENSE-Cog trial

机译:痴呆症中的听力和愿景支持的随机对照试验:感应齿轮试验中的过程评估议定书

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BACKGROUND:Optimising hearing and vision function may be important in improving a range of outcomes for people living with dementia (PwD) and their companions. The SENSE-Cog cross-national randomised controlled trial (RCT) is evaluating the effectiveness of a sensory intervention (SI) to improve quality of life for PwD with concurrent hearing and/or vision impairment, in five European countries. To ascertain how or why the intervention will, or will not, achieve its outcomes, we have designed a process evaluation to explore potential discrepancies between expected and observed outcomes. This will also help us to understand how context may influence the outcomes. Here we describe the protocol for this process evaluation, which is embedded within the RCT.METHODS/DESIGN:We will use a mixed methods approach with a theoretical framework derived from the UK Medical Research Council's' guidance on process evaluations. It will include the following: (1) evaluating how key aspects of the intervention will be delivered, which will be important to scale the intervention in real world populations; (2) characterising the contextual issues, which may shape the delivery and the impact of the intervention in different countries; and (3) investigating possible causal mechanisms through analyses of potential moderators and mediators. To avoid bias, we will analyse the process data before the analysis of the main effectiveness outcomes.DISCUSSION:This evaluation will provide insight into how the complex SENSE-Cog SI will be tailored, enacted and received across the different European contexts, all of which have unique health and social care economies. The findings will provide insight into the causal mechanisms effecting change, and will determine whether we should implement the intervention, if effective, on a wider scale for PwD and concurrent sensory impairment.TRIAL REGISTRATION:ISRCTN, ISRCTN17056211. Registered on 19 February 2018.
机译:背景:优化听证和视觉功能对于改善患有痴呆症(PWD)及其同伴的人的一系列结果可能很重要。 Sense-Cog跨国随机对照试验(RCT)正在评估感官干预(SI)的有效性,以提高PWD的生活质量,并在五个欧洲国家的同时听证和/或视力障碍。为了确定如何或为什么,干预措施或不会实现其结果,我们设计了一个过程评估,以探讨预期和观察结果之间的潜在差异。这也将有助于我们了解背景如何影响结果。在这里,我们描述了该过程评估的协议,该协议嵌入了RCT.Method / Design:我们将使用混合方法方法,并通过英国医学研究委员会的“进程评估指导”的理论框架。它将包括以下内容:(1)评估干预的关键方面是如何交付的,这对于规模在现实世界人口中的干预方面将是重要的; (2)表征上下文问题,可以塑造交付和对不同国家干预的影响; (3)通过分析潜在的主持人和调解员来调查可能的因果机制。为了避免偏见,我们将在分析主要效果成果之前分析过程数据。讨论:这种评估将对复杂的Sense-Cog Si进行洞察,以在不同的欧洲背景下定制,颁布和接受所有这些有独特的健康和社会护理经济体。调查结果将深入了解改变变化的因果机制,并将确定我们是否应该在更广泛的PWD和并发感官损伤方面实施干预,如果有效.Tial注册:ISRCTN,ISRCTN17056211。 2018年2月19日注册。

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