4.7 Article

SPIRIT 2013 Statement: Defining Standard Protocol Items for Clinical Trials

Journal

ANNALS OF INTERNAL MEDICINE
Volume 158, Issue 3, Pages 200-+

Publisher

AMER COLL PHYSICIANS
DOI: 10.7326/0003-4819-158-3-201302050-00583

Keywords

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Funding

  1. Canadian Institutes of Health Research [DET-106068, MET-117434]
  2. Canadian Cancer Society Research Institute
  3. Canadian Agency for Drugs and Technologies in Health
  4. MRC [MC_EX_G0800814] Funding Source: UKRI
  5. Medical Research Council [MC_EX_G0800814] Funding Source: researchfish

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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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