协议(科学)
医学
检查表
报告审判综合标准
临床试验
透明度(行为)
指南
替代医学
可靠性
医学教育
范围(计算机科学)
质量(理念)
研究设计
基础(证据)
医学物理学
家庭医学
病理
计算机科学
心理学
法学
计算机安全
程序设计语言
认知心理学
社会学
哲学
认识论
社会科学
政治学
作者
An‐Wen Chan,Jennifer Tetzlaff,Douglas G. Altman,Andreas Laupacis,Peter C Gøtzsche,Karmela Krleža-Jerić,Asbjørn Hróbjartsson,Howard Mann,Kay Dickersin,Jesse A. Berlin,Caroline J Doré,Wendy R. Parulekar,William Summerskill,Trish Groves,Kenneth F. Schulz,Harold C. Sox,Frank W. Rockhold,Drummond Rennie,David Moher
标识
DOI:10.7326/0003-4819-158-3-201302050-00583
摘要
The protocol of a clinical trial serves as the foundation for study planning, conduct, reporting, and appraisal. However, trial protocols and existing protocol guidelines vary greatly in content and quality. This article describes the systematic development and scope of SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) 2013, a guideline for the minimum content of a clinical trial protocol. The 33-item SPIRIT checklist applies to protocols for all clinical trials and focuses on content rather than format. The checklist recommends a full description of what is planned; it does not prescribe how to design or conduct a trial. By providing guidance for key content, the SPIRIT recommendations aim to facilitate the drafting of high-quality protocols. Adherence to SPIRIT would also enhance the transparency and completeness of trial protocols for the benefit of investigators, trial participants, patients, sponsors, funders, research ethics committees or institutional review boards, peer reviewers, journals, trial registries, policymakers, regulators, and other key stakeholders.
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