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      Views of Ethical Best Practices in Sharing Individual-Level Data From Medical and Public Health Research : A Systematic Scoping Review

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          Abstract

          There is increasing support for sharing individual-level data generated by medical and public health research. This scoping review of empirical research and conceptual literature examined stakeholders’ perspectives of ethical best practices in data sharing, particularly in low- and middle-income settings. Sixty-nine empirical and conceptual articles were reviewed, of which, only five were empirical studies and eight were conceptual articles focusing on low- and middle-income settings. We conclude that support for sharing individual-level data is contingent on the development and implementation of international and local policies and processes to support ethical best practices. Further conceptual and empirical research is needed to ensure data sharing policies and processes in low- and middle-income settings are appropriately informed by stakeholders’ perspectives.

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          Most cited references59

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          Cochrane Update. 'Scoping the scope' of a cochrane review.

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            Prepublication data sharing.

            Rapid release of prepublication data has served the field of genomics well. Attendees at a workshop in Toronto recommend extending the practice to other biological data sets.
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              Preparing for responsible sharing of clinical trial data.

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                Author and article information

                Journal
                J Empir Res Hum Res Ethics
                J Empir Res Hum Res Ethics
                JRE
                spjre
                Journal of Empirical Research on Human Research Ethics
                SAGE Publications (Sage CA: Los Angeles, CA )
                1556-2646
                1556-2654
                July 2015
                July 2015
                : 10
                : 3 , Special issue: Ethics and sharing individual-level health research data from low and middle income settings
                : 225-238
                Affiliations
                [1 ]University of Oxford, UK
                Author notes
                [*]Susan Bull, Ethox Centre, Nuffield Department of Population Health, University of Oxford, Old Road Campus, Oxford OX3 7LF, UK. Email: susan.bull@ 123456ethox.ox.ac.uk
                Article
                10.1177_1556264615594767
                10.1177/1556264615594767
                4548478
                26297745
                5f08d8b1-f690-4248-af96-6c2b3a6474f9
                © The Author(s) 2015

                This article is distributed under the terms of the Creative Commons Attribution 3.0 License ( http://www.creativecommons.org/licenses/by/3.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                Categories
                Ethics and Best Practices in Data Sharing in Low and Middle Income Settings

                biomedical research ethics,data sharing,data release,data access,research data,research governance,low-income countries,middle-income countries,clinical research,health policy,privacy,systematic review

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