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Current practice in methodology and reporting of the sample size calculation in randomised trials of hip and knee osteoarthritis: a protocol for a systematic review

机译:髋关节和膝关节骨关节炎随机试验的方法学和报告样本量计算的当前实践:系统评价的方案

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Background A key aspect of the design of randomised controlled trials (RCTs) is determining the sample size. It is important that the trial sample size is appropriately calculated. The required sample size will differ by clinical area, for instance, due to the prevalence of the condition and the choice of primary outcome. Additionally, it will depend upon the choice of target difference assumed in the calculation. Focussing upon the hip and knee osteoarthritis population, this study aims to systematically review how the trial size was determined for trials of osteoarthritis, on what basis, and how well these aspects are reported. Methods Several electronic databases (Medline, Cochrane library, CINAHL, EMBASE, PsycINFO, PEDro and AMED) will be searched to identify articles on RCTs of hip and knee osteoarthritis published in 2016. Articles will be screened for eligibility and data extracted independently by two reviewers. Data will be extracted on study characteristics (design, population, intervention and control treatments), primary outcome, chosen sample size and justification, parameters used to calculate the sample size (including treatment effect in control arm, level of variability in primary outcome, loss to follow-up rates). Data will be summarised across the studies using appropriate summary statistics (e.g. n and %, median and interquartile range). The proportion of studies which report each key component of the sample size calculation will be presented. The reproducibility of the sample size calculation will be tested. Discussion The findings of this systematic review will summarise the current practice for sample size calculation in trials of hip and knee osteoarthritis. It will also provide evidence on the completeness of the reporting of the sample size calculation, reproducibility of the chosen sample size and the basis for the values used in the calculation. Trial registration As this review was not eligible to be registered on PROSPERO, the summary information was uploaded to Figshare to make it publicly accessible in order to avoid unnecessary duplication amongst other benefits ( https://doi.org/10.6084/m9.figshare.5009027.v1) ; Registered January 17, 2017.
机译:背景技术随机对照试验(RCT)设计的一个关键方面是确定样本量。重要的是要适当地计算试验样本的大小。例如,由于疾病的患病率和主要结局的选择,所需的样本量会因临床领域而异。另外,这将取决于计算中假设的目标差异的选择。本研究针对髋关节和膝关节骨关节炎人群,旨在系统地回顾如何确定骨关节炎试验的试验规模,在什么基础上以及这些方面的报道情况。方法将检索多个电子数据库(Medline,Cochrane库,CINAHL,EMBASE,PsycINFO,PEDro和AMED),以鉴定2016年发表的有关髋关节和膝关节骨关节炎的RCT的文章。将对这些文章进行筛选,并由两名审阅者独立提取数据。将提取以下数据:研究特征(设计,人群,干预和对照治疗),主要结局,所选样本量和合理性,用于计算样本量的参数(包括对照组的治疗效果,主要结局的变异水平,损失) (随访率)。将使用适当的摘要统计数据(例如n和%,中位数和四分位数范围)汇总研究中的数据。将介绍报告样本量计算的每个关键组成部分的研究比例。将测试样本量计算的可重复性。讨论该系统评价的结果将总结髋和膝骨关节炎试验中样本量计算的当前实践。它还将提供有关样本量计算报告的完整性,所选样本量的可重复性以及计算所用值的依据的证据。试用注册由于此评论不符合在PROSPERO上注册的条件,因此摘要信息已上载到Figshare以使其可公开访问,从而避免了其他好处之间的不必要重复(https://doi.org/10.6084/m9.figshare。 5009027.v1); 2017年1月17日注册。

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