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Reflections on dynamic consent in biomedical research: the story so far
Harriet J A Teare1, Megan Prictor2, Jane Kaye3,2
1Centre for Health, Law and Emerging Technologies, Faculty of Law, University of Oxford, Oxford, UK. harriet.teare@law.ox.ac.uk.
Abstract:
Dynamic consent (DC) was originally developed in response to challenges to the informed consent process presented by participants agreeing to 'future research' in biobanking. In the past 12 years, it has been trialled in a number of different projects, and examined as a new approach for consent and to support patient engagement over time. There have been significant societal shifts during this time, namely in our reliance on digital tools and the use of social media, as well as a greater appreciation of the integral role of patients in biomedical research. This paper reflects on the development of DC to understand its importance in an age where digital health is becoming the norm and patients require greater oversight and control of how their data may be used in a range of settings. As well as looking back, it looks forwards to consider how DC could be further utilised to enhance the patient experience and address some of the inequalities caused by the digital divide in society.
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