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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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| Publicado no: | PLoS One |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2020
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| Assuntos: | |
| Acesso em linha: | 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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