Ethical sharing of health data in online platforms – which values should be considered?

Detalhes bibliográficos
Autor(a) principal: Riso, B.
Data de Publicação: 2017
Outros Autores: Tupasela, A., Vears, D. F., Felzmann, H., Cockbain, J., Loi, M., Kongsholm, N. C. H., Zullo, S., Rakic, V.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10071/14284
Resumo: Intensified and extensive data production and data storage are characteristics of contemporary western societies. Health data sharing is increasing with the growth of Information and Communication Technology (ICT) platforms devoted to the collection of personal health and genomic data. However, the sensitive and personal nature of health data poses ethical challenges when data is disclosed and shared even if for scientific research purposes. With this in mind, the Science and Values Working Group of the COST Action CHIP ME ‘Citizen's Health through public-private Initiatives: Public health, Market and Ethical perspectives’ (IS 1303) identified six core values they considered to be essential for the ethical sharing of health data using ICT platforms. We believe that using this ethical framework will promote respectful scientific practices in order to maintain individuals’ trust in research. We use these values to analyse five ICT platforms and explore how emerging data sharing platforms are reconfiguring the data sharing experience from a range of perspectives. We discuss which types of values, rights and responsibilities they entail and enshrine within their philosophy or outlook on what it means to share personal health information. Through this discussion we address issues of the design and the development process of personal health data and patient-oriented infrastructures, as well as new forms of technologically-mediated empowerment.
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spelling Ethical sharing of health data in online platforms – which values should be considered?Data sharingEthical valuesHealth dataHealth researchInformation and communication technology platformsInteroperabilityIntensified and extensive data production and data storage are characteristics of contemporary western societies. Health data sharing is increasing with the growth of Information and Communication Technology (ICT) platforms devoted to the collection of personal health and genomic data. However, the sensitive and personal nature of health data poses ethical challenges when data is disclosed and shared even if for scientific research purposes. With this in mind, the Science and Values Working Group of the COST Action CHIP ME ‘Citizen's Health through public-private Initiatives: Public health, Market and Ethical perspectives’ (IS 1303) identified six core values they considered to be essential for the ethical sharing of health data using ICT platforms. We believe that using this ethical framework will promote respectful scientific practices in order to maintain individuals’ trust in research. We use these values to analyse five ICT platforms and explore how emerging data sharing platforms are reconfiguring the data sharing experience from a range of perspectives. We discuss which types of values, rights and responsibilities they entail and enshrine within their philosophy or outlook on what it means to share personal health information. Through this discussion we address issues of the design and the development process of personal health data and patient-oriented infrastructures, as well as new forms of technologically-mediated empowerment.SpringerOpen2017-08-29T10:12:18Z2017-01-01T00:00:00Z20172019-04-02T10:44:13Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10071/14284eng2195-781910.1186/s40504-017-0060-zRiso, B.Tupasela, A.Vears, D. F.Felzmann, H.Cockbain, J.Loi, M.Kongsholm, N. C. H.Zullo, S.Rakic, V.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-09T17:31:51Zoai:repositorio.iscte-iul.pt:10071/14284Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T22:14:20.159249Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Ethical sharing of health data in online platforms – which values should be considered?
title Ethical sharing of health data in online platforms – which values should be considered?
spellingShingle Ethical sharing of health data in online platforms – which values should be considered?
Riso, B.
Data sharing
Ethical values
Health data
Health research
Information and communication technology platforms
Interoperability
title_short Ethical sharing of health data in online platforms – which values should be considered?
title_full Ethical sharing of health data in online platforms – which values should be considered?
title_fullStr Ethical sharing of health data in online platforms – which values should be considered?
title_full_unstemmed Ethical sharing of health data in online platforms – which values should be considered?
title_sort Ethical sharing of health data in online platforms – which values should be considered?
author Riso, B.
author_facet Riso, B.
Tupasela, A.
Vears, D. F.
Felzmann, H.
Cockbain, J.
Loi, M.
Kongsholm, N. C. H.
Zullo, S.
Rakic, V.
author_role author
author2 Tupasela, A.
Vears, D. F.
Felzmann, H.
Cockbain, J.
Loi, M.
Kongsholm, N. C. H.
Zullo, S.
Rakic, V.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Riso, B.
Tupasela, A.
Vears, D. F.
Felzmann, H.
Cockbain, J.
Loi, M.
Kongsholm, N. C. H.
Zullo, S.
Rakic, V.
dc.subject.por.fl_str_mv Data sharing
Ethical values
Health data
Health research
Information and communication technology platforms
Interoperability
topic Data sharing
Ethical values
Health data
Health research
Information and communication technology platforms
Interoperability
description Intensified and extensive data production and data storage are characteristics of contemporary western societies. Health data sharing is increasing with the growth of Information and Communication Technology (ICT) platforms devoted to the collection of personal health and genomic data. However, the sensitive and personal nature of health data poses ethical challenges when data is disclosed and shared even if for scientific research purposes. With this in mind, the Science and Values Working Group of the COST Action CHIP ME ‘Citizen's Health through public-private Initiatives: Public health, Market and Ethical perspectives’ (IS 1303) identified six core values they considered to be essential for the ethical sharing of health data using ICT platforms. We believe that using this ethical framework will promote respectful scientific practices in order to maintain individuals’ trust in research. We use these values to analyse five ICT platforms and explore how emerging data sharing platforms are reconfiguring the data sharing experience from a range of perspectives. We discuss which types of values, rights and responsibilities they entail and enshrine within their philosophy or outlook on what it means to share personal health information. Through this discussion we address issues of the design and the development process of personal health data and patient-oriented infrastructures, as well as new forms of technologically-mediated empowerment.
publishDate 2017
dc.date.none.fl_str_mv 2017-08-29T10:12:18Z
2017-01-01T00:00:00Z
2017
2019-04-02T10:44:13Z
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10.1186/s40504-017-0060-z
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