Epidemiology and Informed Consent
Epidemiology and Informed Consent
Informed consent is a central concept and practice in the protection of both patients receiving clinical care and individuals participating in research. What began as a commitment to ethical principles has found its way into legal cases concerning the physician-patient relationship, federal policy, and international standards for ethical research on human subjects. Given the tension between informed consent and much of epidemiology, this chapter analyzes three core questions: (1) Does epidemiology require informed consent? If so, (2) why and under what conditions? Finally, (3) what special issues, if any, does epidemiology raise for the concept and practice of informed consent?.
Keywords: epidemiology, informed consent, epidemiological research, self-determination, ethical principles
Oxford Scholarship Online requires a subscription or purchase to access the full text of books within the service. Public users can however freely search the site and view the abstracts and keywords for each book and chapter.
Please, subscribe or login to access full text content.
If you think you should have access to this title, please contact your librarian.
To troubleshoot, please check our FAQs , and if you can't find the answer there, please contact us .