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Data Protection in Sociological Health Research

A Critical Narrative about the Challenges of a New Regulatory Landscape

Dados Bibliográficos

ID2392278
AutoresHélder Raposo (0000-0002-3614-5661, Lisbon School of Health Technology – Polytechnic Institute of Lisbon, Portugal, autor correspondente), Sara Melo (0000-0001-5663-6997, Higher Institute of Social Work of Oporto, Portugal), Catarina Egreja (0000-0003-1396-1102, Centro de Investigação Interdisciplinar Egas Moniz (CiiEM), Instituto Universitário Egas Moniz (IUEM), Monte de Caparica, Portugal)
Ano2022
Volume27
Fascículo4
Páginas1060-1076
Data de publicação2022-12-01
Peer ReviewedSim
Open AccessSim
TipoARTICLE
PeriódicoSociological Research Online (JOURNAL)
Identificadores do periódicoISSN: 1360-7804 • E-ISSN: 1360-7804
EditoraSAGE Publications Inc (PUBLISHER)
DOI10.1177/13607804221107676
OpenAlexW4296182489
IdiomaEN
Citações recebidas3
Referências citadas40

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 an 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

Business · Data Protection Act 1998 · Engineering ethics · General Data Protection Regulation · Knowledge management · Narrative · Political science · Public relations · Sociology · Computer Science · Data Analysis and Archiving · Ethics in Clinical Research · Focus Groups and Qualitative Methods · Law

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Obras citantes distintas3
Citações por ano1,5
Intervalo de citações2024 - 2026 (3)
Velocidade de citaçãocurrent
Altamente citadoNão
Tipos de citaçãoNeutras: 3
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