Abstract
Clinical trial data-sharing is seen as an imperative for research integrity and is becoming increasingly encouraged or even required by funders, journals, and other stakeholders. However, early experiences with data-sharing have been disappointing because they are not always conducted properly. Health data is indeed sensitive and not always easy to share in a responsible way. We propose 10 rules for researchers wishing to share their data. These rules cover the majority of elements to be considered in order to start the commendable process of clinical trial data-sharing:
Rule 1: Abide by local legal and regulatory data protection requirements
Rule 2: Anticipate the possibility of clinical trial data-sharing before obtaining funding
Rule 3: Declare your intent to share data in the registration step
Rule 4: Involve research participants
Rule 5: Determine the method of data access
Rule 6: Remember there are several other elements to share
Rule 7: Do not proceed alone
Rule 8: Deploy optimal data management to ensure that the data shared is useful
Rule 9: Minimize risks
Rule 10: Strive for excellence.
Funder
Ministère de l'Enseignement Supérieur, de la Recherche et de l'Innovation
Publisher
Public Library of Science (PLoS)
Subject
Computational Theory and Mathematics,Cellular and Molecular Neuroscience,Genetics,Molecular Biology,Ecology,Modeling and Simulation,Ecology, Evolution, Behavior and Systematics
Reference37 articles.
1. OSTP Issues Guidance to Make Federally Funded Research Freely Available Without Delay | OSTP;In: The White House,2022
2. Sharing Clinical Trial Data: A Proposal from the International Committee of Medical Journal Editors;DB Taichman;PLoS Med,2016
3. Medical journal requirements for clinical trial data sharing: Ripe for improvement;F Naudet;PLoS Med,2021
4. International Comparative Legal Guides. In: International Comparative Legal Guides International Business Reports;GL Group;Global Legal Group,2022
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