Guidelines for the content of statistical analysis plans in clinical trials: protocol for an extension to cluster randomized trials.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Trials Pub Date : 2025-02-27 DOI:10.1186/s13063-025-08756-3
Karla Hemming, Jacqueline Y Thompson, Richard L Hooper, Obioha C Ukoumunne, Fan Li, Agnes Caille, Brennan C Kahan, Clemence Leyrat, Michael J Grayling, Nuredin I Mohammed, Jennifer A Thompson, Bruno Giraudeau, Elizabeth L Turner, Samuel I Watson, Beatriz Goulão, Jessica Kasza, Andrew B Forbes, Andrew J Copas, Monica Taljaard
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Abstract

Background: Guidance exists to inform the content of statistical analysis plans in clinical trials. Though not explicitly stated, this guidance is generally focused on clinical trials in which the randomization units are individual patients and not groups of patients. There are critical considerations for the analysis of cluster randomized trials, such as accounting for clustering, the risk of imbalances between the arms due to post-randomization recruitment, and the need to use small sample corrections when the number of clusters is small.

Methods: This paper outlines the protocol for the development of a set of reporting guidelines for the content of statistical analysis plans for cluster randomized trials (including variations such as the stepped wedge cluster randomized trial and other cluster cross-over designs) by extending the minimum reporting analysis requirements as previously defined for individually randomized trials to cluster randomized trials. The guideline will be developed using a consensus-based approach, modifying existing reporting items from the guideline for individually randomized trials and extending to include new items.

Discussion: The guideline will be developed so it can be used independently of the guideline for individually randomized designs. The consensus guidelines will be published in an open-access journal, including key guidance as well as exploration and elaboration.

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临床试验中统计分析计划内容指南:扩展到聚类随机试验的方案。
背景:指南的存在是为了告知临床试验中统计分析计划的内容。虽然没有明确说明,但该指南通常侧重于随机分组单位为单个患者而不是患者组的临床试验。对于聚类随机试验的分析,有一些关键的考虑因素,如聚类的计算、随机化后招募导致各组间不平衡的风险,以及在聚类数量较少时使用小样本校正的必要性。方法:本文通过将先前为单个随机试验定义的最低报告分析要求扩展到聚类随机试验,概述了为聚类随机试验(包括阶梯楔形聚类随机试验和其他聚类交叉设计等变体)的统计分析计划内容制定一套报告指南的协议。该指南将采用基于共识的方法制定,修改指南中针对个别随机试验的现有报告项目,并扩展到包括新项目。讨论:该指南将被开发,以便它可以独立于单独随机设计的指南使用。协商一致的指导方针将在一份开放获取的期刊上发表,其中包括关键指导以及探索和阐述。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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