Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.21/14993 |
Resumo: | The recent implementation of the General Data Protection Regulation (GDPR) establishes a set of formal requirements that reinforce personal data protection, namely, those concerning the collection, treatment, and dissemination of data on research participants. With the application of this new legal provision at the European level, new types of restrictions are emerging, whose nature and reach intensify the tension between demands for privacy and scientific freedom in research. In this article, we take as a reference ongoing research taking place in Portugal, in the field of Sociology of Health, concerning the consumption of medicines by professionals exposed to high-performance pressure. Our main objective is to identify and analyse the implications of regulatory challenges faced in the research process and how the researchers managed and overcame them. We present a critical narrative that sheds light on the nature of the choices taken while also assessing the practical implications for the operationalisation of the research. We conclude by noting that, despite the benefits that may flow from the application of GDPR, the new requirements regarding the protection of personal data may override the ethical principles of scientific research and strengthen regulatory restrictions on conducting research. In the research concerned, the significant practical implications were indirect access to participants, a more time-consuming process in terms of participant adherence, and a temporal discrepancy between the different stages of recruitment. |
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Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscapeData protectionRegulatory challengesResearch ethicsSociological health researchThe recent implementation of the General Data Protection Regulation (GDPR) establishes a set of formal requirements that reinforce personal data protection, namely, those concerning the collection, treatment, and dissemination of data on research participants. With the application of this new legal provision at the European level, new types of restrictions are emerging, whose nature and reach intensify the tension between demands for privacy and scientific freedom in research. In this article, we take as a reference ongoing research taking place in Portugal, in the field of Sociology of Health, concerning the consumption of medicines by professionals exposed to high-performance pressure. Our main objective is to identify and analyse the implications of regulatory challenges faced in the research process and how the researchers managed and overcame them. We present a critical narrative that sheds light on the nature of the choices taken while also assessing the practical implications for the operationalisation of the research. We conclude by noting that, despite the benefits that may flow from the application of GDPR, the new requirements regarding the protection of personal data may override the ethical principles of scientific research and strengthen regulatory restrictions on conducting research. In the research concerned, the significant practical implications were indirect access to participants, a more time-consuming process in terms of participant adherence, and a temporal discrepancy between the different stages of recruitment.SageRCIPLRaposo, Hélder AntónioMelo, SaraEgreja, Catarina2022-09-29T12:00:48Z2022-122022-12-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.21/14993engRaposo H, Melo S, Egreja C. Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape. Sociol Res Online. 2022;27(4):1060-76.10.1177/13607804221107676info: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:RCAAP2023-09-06T02:15:49Zoai:repositorio.ipl.pt:10400.21/14993Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:22:44.488758Repositório 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 |
Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape |
title |
Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape |
spellingShingle |
Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape Raposo, Hélder António Data protection Regulatory challenges Research ethics Sociological health research |
title_short |
Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape |
title_full |
Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape |
title_fullStr |
Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape |
title_full_unstemmed |
Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape |
title_sort |
Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape |
author |
Raposo, Hélder António |
author_facet |
Raposo, Hélder António Melo, Sara Egreja, Catarina |
author_role |
author |
author2 |
Melo, Sara Egreja, Catarina |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
RCIPL |
dc.contributor.author.fl_str_mv |
Raposo, Hélder António Melo, Sara Egreja, Catarina |
dc.subject.por.fl_str_mv |
Data protection Regulatory challenges Research ethics Sociological health research |
topic |
Data protection Regulatory challenges Research ethics Sociological health research |
description |
The recent implementation of the General Data Protection Regulation (GDPR) establishes a set of formal requirements that reinforce personal data protection, namely, those concerning the collection, treatment, and dissemination of data on research participants. With the application of this new legal provision at the European level, new types of restrictions are emerging, whose nature and reach intensify the tension between demands for privacy and scientific freedom in research. In this article, we take as a reference ongoing research taking place in Portugal, in the field of Sociology of Health, concerning the consumption of medicines by professionals exposed to high-performance pressure. Our main objective is to identify and analyse the implications of regulatory challenges faced in the research process and how the researchers managed and overcame them. We present a critical narrative that sheds light on the nature of the choices taken while also assessing the practical implications for the operationalisation of the research. We conclude by noting that, despite the benefits that may flow from the application of GDPR, the new requirements regarding the protection of personal data may override the ethical principles of scientific research and strengthen regulatory restrictions on conducting research. In the research concerned, the significant practical implications were indirect access to participants, a more time-consuming process in terms of participant adherence, and a temporal discrepancy between the different stages of recruitment. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-09-29T12:00:48Z 2022-12 2022-12-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.21/14993 |
url |
http://hdl.handle.net/10400.21/14993 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Raposo H, Melo S, Egreja C. Data protection in sociological health research: a critical narrative about the challenges of a new regulatory landscape. Sociol Res Online. 2022;27(4):1060-76. 10.1177/13607804221107676 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Sage |
publisher.none.fl_str_mv |
Sage |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1817553324912672768 |