SPIRIT 2025声明

JAMA Pub Date : 2025-04-28 DOI:10.1001/jama.2025.4486
An-Wen Chan, Isabelle Boutron, Sally Hopewell, David Moher, Kenneth F. Schulz, Gary S. Collins, Ruth Tunn, Rakesh Aggarwal, Michael Berkwits, Jesse A. Berlin, Nita Bhandari, Nancy J. Butcher, Marion K. Campbell, Runcie C. W. Chidebe, Diana R. Elbourne, Andrew J. Farmer, Dean A. Fergusson, Robert M. Golub, Steven N. Goodman, Tammy C. Hoffmann, John P. A. Ioannidis, Brennan C. Kahan, Rachel L. Knowles, Sarah E. Lamb, Steff Lewis, Elizabeth Loder, Martin Offringa, Philippe Ravaud, Dawn P. Richards, Frank W. Rockhold, David L. Schriger, Nandi L. Siegfried, Sophie Staniszewska, Rod S. Taylor, Lehana Thabane, David J. Torgerson, Sunita Vohra, Ian R. White, Asbjørn Hróbjartsson
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引用次数: 0

摘要

重要性随机试验方案是研究计划、实施、报告和外部评价的基础。然而,试验方案的完整性各不相同,而且往往不涉及设计和实施的关键要素。SPIRIT(标准方案项目:干预性试验建议)声明于2013年首次发布,作为提高试验方案完整性的指南。需要定期更新,纳入最新证据和最佳做法,以确保指南与用户保持相关性。在此,我们系统地更新了SPIRIT关于随机试验方案中最小项目的建议。我们完成了一项范围审查,并开发了一个项目特定的经验和理论证据数据库,以生成SPIRIT 2013检查表的潜在变化列表。现有的SPIRIT/CONSORT(综合试验报告标准)扩展(危害、结果、非药物治疗)和其他报告指南(干预描述和复制模板[TIDieR])的主要作者提供的建议丰富了该列表。潜在的修改是在一个3轮德尔菲调查之后的共识会议进行评级。总共有317人参与了德尔菲共识过程,30位专家参加了共识会议。该过程导致增加了2个新的议定书项目,修订了5个项目,删除/合并了5个项目,并整合了其他相关报告指南的关键项目。值得注意的变化包括新的开放科学部分,额外强调危害评估和干预措施和比较物的描述,以及关于患者和公众如何参与试验设计、实施和报告的新项目。更新后的SPIRIT 2025声明包括一份基于证据的清单,其中包含试验方案中需要解决的34个最低项目,以及说明试验参与者的入组、干预措施和评估时间表的图表。为方便实施,我们亦制定了“精神2025”清单的扩展版本,以及随附的解释和阐述文件。结论和相关性更新后的SPIRIT 2025声明的广泛认可和遵守有可能提高试验方案的透明度和完整性,从而使研究者、试验参与者、患者、资助者、研究伦理委员会、期刊、试验注册中心、政策制定者、监管机构和其他审稿人受益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SPIRIT 2025 Statement
ImportanceThe protocol of a randomized trial is the foundation for study planning, conduct, reporting, and external review. However, trial protocols vary in their completeness and often do not address key elements of design and conduct. The SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) statement was first published in 2013 as guidance to improve the completeness of trial protocols. Periodic updates incorporating the latest evidence and best practices are needed to ensure that the guidance remains relevant to users. Herein, we systematically update the SPIRIT recommendations for minimum items to address in the protocol of a randomized trial.ObservationsWe completed a scoping review and developed a project specific database of empirical and theoretical evidence to generate a list of potential changes to the SPIRIT 2013 checklist. The list was enriched with recommendations provided by lead authors of existing SPIRIT/CONSORT (Consolidated Standards of Reporting Trials) extensions (harms, outcomes, nonpharmacological treatment) and other reporting guidelines (Template for Intervention Description and Replication [TIDieR]). The potential modifications were rated in a 3-round Delphi survey followed by a consensus meeting. Overall, 317 individuals participated in the Delphi consensus process and 30 experts attended the consensus meeting. The process led to the addition of 2 new protocol items, revision to 5 items, deletion/merger of 5 items, and integration of key items from other relevant reporting guidelines. Notable changes include a new open-science section, additional emphasis on the assessment of harms and description of interventions and comparators, and a new item on how patients and the public will be involved in trial design, conduct, and reporting. The updated SPIRIT 2025 statement consists of an evidence based checklist of 34 minimum items to address in a trial protocol, along with a diagram illustrating the schedule of enrollment, interventions, and assessments for trial participants. To facilitate implementation, we also developed an expanded version of the SPIRIT 2025 checklist and an accompanying explanation and elaboration document.Conclusions and RelevanceWidespread endorsement and adherence to the updated SPIRIT 2025 statement have the potential to enhance the transparency and completeness of trial protocols for the benefit of investigators, trial participants, patients, funders, research ethics committees, journals, trial registries, policy makers, regulators, and other reviewers.
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