Study Design Guidelines
- 作者: Sereda A.P.1, Andrianova M.A.1
-
隶属关系:
- Federal Medical and Biological Agency
- 期: 卷 25, 编号 3 (2019)
- 页面: 165-184
- 栏目: FOR RESEARCHERS
- ##submission.dateSubmitted##: 18.10.2019
- ##submission.dateAccepted##: 18.10.2019
- ##submission.datePublished##: 18.10.2019
- URL: https://journal.rniito.org/jour/article/view/1310
- DOI: https://doi.org/10.21823/2311-2905-2019-25-3-165-184
- ID: 1310
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详细
Complying with certain requirements or, more precisely, following the guidelines for the design of a scientific publication helps to make it not only more comprehensible for reviewers and readers, but actually enhances the quality of work. For example, even if some aspects in design logic were fulfilled but not described, other researchers doing meta-analysis may wrongly but for a good reason downgrade such publication and exclude it from the analysis. Understanding of the guidelines for study design ensures not only the proper description of the results but the initial planning of work. The CA RE guidelines were established for reporting of clinical cases, STROBE — for reporting observational studies (cohort and case-control studies), CO NSORT — for reporting randomized studies (these guidelines are often used also for other comparative and case series studies), STARD — for reporting diagnostic studies, and PRISMA — for reporting of systematic reviews and meta-analyses. The present paper describes the key aspects of those guidelines and provides templates for graphic display of study design in form of flow charts. Evidently, we should not forget that each study is unique and there is always a place for a reasonable compromise between “requirements” and the real logic of the research in place.
作者简介
A. Sereda
Federal Medical and Biological Agency
编辑信件的主要联系方式.
Email: drsereda@gmail.com
Dr. Sci. (Med.), Deputy Head
Moscow
俄罗斯联邦M. Andrianova
Federal Medical and Biological Agency
Email: fake@neicon.ru
Cand. Sci. (Tech.), Consultant, Department of Health and Industrial Medicine
Moscow
俄罗斯联邦参考
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