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Statistical analysis and handling of missing data in cluster randomised trials: protocol for a systematic review

机译:整群随机试验中的统计分析和缺失数据处理:系统评价方案

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Introduction Cluster randomised trials (CRTs) randomise participants in groups, rather than as individuals, and are key tools used to assess interventions in health research where treatment contamination is likely or if individual randomisation is not feasible. Missing outcome data can reduce power in trials, including in CRTs, and is a potential source of bias. The current review focuses on evaluating methods used in statistical analysis and handling of missing data with respect to the primary outcome in CRTs. Methods and analysis We will search for CRTs published between August 2013 and July 2014 using PubMed, Web of Science and PsycINFO. We will identify relevant studies by screening titles and abstracts, and examining full-text articles based on our predefined study inclusion criteria. 86 studies will be randomly chosen to be included in our review. Two independent reviewers will collect data from each study using a standardised, prepiloted data extraction template. Our findings will be summarised and presented using descriptive statistics. Ethics and dissemination This methodological systematic review does not need ethical approval because there are no data used in our study that are linked to individual patient data. After completion of this systematic review, data will be immediately analysed, and findings will be disseminated through a peer-reviewed publication and conference presentation.
机译:简介群集随机试验(CRT)将参与者(而不是个人)随机分组,并且是评估可能会受到治疗污染或个体随机化的健康研究干预措施的关键工具。缺少结果数据可能会降低包括CRT在内的试验的功效,并且可能是造成偏见的原因。本次审查的重点是针对CRT的主要结果,评估用于统计分析和处理缺失数据的方法。方法和分析我们将使用PubMed,Web of Science和PsycINFO搜索2013年8月至2014年7月之间发布的CRT。我们将通过筛选标题和摘要,并根据我们预定义的研究纳入标准来检查全文,从而确定相关研究。我们将随机选择86项研究纳入我们的评价。两名独立的审阅者将使用标准化的预试数据提取模板从每个研究中收集数据。我们的发现将使用描述性统计数据进行汇总和介绍。伦理与传播本方法学的系统评价不需要伦理学的认可,因为在我们的研究中没有使用与个体患者数据相关的数据。在完成此系统评价后,将立即分析数据,并通过同行评审的出版物和会议演示文稿分发调查结果。

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