Standards for design and measurement would make clinical research reproducible and usable

被引:16
作者
Dickersin, Kay [1 ]
Mayo-Wilson, Evan [1 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
关键词
clinical trials; systematic reviews; open science; data sharing; scientific standards; INTERNATIONAL-COMMITTEE; TRIAL REGISTRATION; SYSTEMATIC REVIEWS; REDUCING WASTE; STATEMENT; DATABASE; OUTCOMES; UPDATE;
D O I
10.1073/pnas.1708273114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We find standards useful in everyday life and in science, although we do not always follow them. Adopting new standards can be expensive, so there may be a strong incentive to maintain the status quo rather than adopt new standards. The scientific community has many standards encompassing both doing clinical research and reporting it, including standards for design and measurement. Although existing research standards have improved both research and its reporting, we need to unify existing standards and to fill the gaps between steps throughout the research process. Existing gaps include implementation of standards and links between standards for study registration (to know about all studies undertaken), study protocols (to identify the preplanned study design and methods), data collection (to assess outcomes that are important and comparable across studies), dissemination of findings (to know the results of previous studies), data sharing (to make best use of existing data), and evidence synthesis (to draw appropriate conclusions from the body of evidence). The scientific community must work together to harmonize existing standards, to ensure that standards are kept up to date, to check that standards are followed, and to develop standards where they are still needed. A unified system of standards will make our work more reproducible.
引用
收藏
页码:2590 / 2594
页数:5
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