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Do people have an ethical obligation to share their health information? Comparing narratives of altruism and health information sharing in a nationally representative sample

BACKGROUND: With the emergence of new health information technologies, health information can be shared across networks, with or without patients’ awareness and/or their consent. It is often argued that there can be an ethical obligation to participate in biomedical research, motivated by altruism,...

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Veröffentlicht in:PLoS One
Hauptverfasser: Raj, Minakshi, De Vries, Raymond, Nong, Paige, Kardia, Sharon L. R., Platt, Jodyn E.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Public Library of Science 2020
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Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7774955/
https://ncbi.nlm.nih.gov/pubmed/33382835
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0244767
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