Published on in Vol 25 (2023)

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/46306, first published .
Testing and Practical Implementation of a User-Friendly Personalized and Long-Term Electronic Informed Consent Prototype in Clinical Research: Mixed Methods Study

Testing and Practical Implementation of a User-Friendly Personalized and Long-Term Electronic Informed Consent Prototype in Clinical Research: Mixed Methods Study

Testing and Practical Implementation of a User-Friendly Personalized and Long-Term Electronic Informed Consent Prototype in Clinical Research: Mixed Methods Study

Evelien De Sutter   1 , PhD ;   David Geerts   2 , PhD ;   Koen Yskout   3 , Prof Dr ;   Stef Verreydt   3 , MSc ;   Pascal Borry   4 , Prof Dr ;   Liese Barbier   1 , PhD ;   Isabelle Huys   1 , Prof Dr

1 Clinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, Catholic University (KU) Leuven, Leuven, Belgium

2 Catholic University (KU) Leuven Digital Society Institute, Catholic University (KU) Leuven, Leuven, Belgium

3 imec-DistriNet, Catholic University (KU) Leuven, Leuven, Belgium

4 Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, Catholic University (KU) Leuven, Leuven, Belgium

Corresponding Author:

  • David Geerts, PhD
  • Catholic University (KU) Leuven Digital Society Institute
  • Catholic University (KU) Leuven
  • Parkstraat 45
  • Box 3605
  • Leuven, 3000
  • Belgium
  • Phone: 32 16323195
  • Email: david.geerts@kuleuven.be