Authors:
Simon Geller
1
;
Sebastian Müller
2
;
Simon Scheider
1
;
Christiane Woopen
3
;
2
and
Sven Meister
4
;
1
Affiliations:
1
Healthcare, Fraunhofer Institute of Software and Systems Engineering, Emil-Figge-Straße 91, 44227 Dortmund, Germany
;
2
ceres, University of Cologne, Albertus-Magnus-Platz, 50923 Cologne, Germany
;
3
Center for Life Ethics, University Bonn, Schaumburg-Lippe-Str. 7, 53113 Bonn, Germany
;
4
Department of Health/School of Medicine, Witten/Herdecke University, Alfred-Herrhausen-Straße 50, 58455 Witten, Germany
Keyword(s):
Consent Model, Electronic Health Records, Big Data, Autonomy, Moral Values, Medical Research, Privacy, Meta Consent.
Abstract:
Due to new technological innovations, the increase in lifestyle products, and the digitalisation of healthcare the volume of personal health data is constantly growing. However, in order to use, re-use, and link personalised health data and, thus, unlock their potential benefits in health research, the authors of the data need to voluntarily give their informed consent. That is a major challenge to health data research, because the classic informed consent process requires the immense administrative burden to ask for consent, every time personal health data is accessed. In this paper we argue that all alternative consent models that have been developed to tackle this problem, either do not reduce administrative burdens significantly or do not conform to the informed consent ideal. That is why we used the design thinking approach to develop an alternative consent model that we call the value-based consent model. This model has the potential to reduce administrative burdens while empow
ering research subjects to autonomously translate their values into consent decisions.
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