Gude, Wouter T.
Roos-Blom, Marie-José
van der Veer, Sabine N.
Dongelmans, Dave A.
de Jonge, Evert
Francis, Jill J.
Peek, Niels
de Keizer, Nicolette F.
Funding for this research was provided by:
Medical Research Council (MR/K006665/1)
Article History
Received: 1 December 2017
Accepted: 6 February 2018
First Online: 17 February 2018
Ethics approval and consent to participate
: The Institutional Review Board (IRB) of the Academic Medical Center (Amsterdam, the Netherlands) informed us that formal IRB approval and patient consent was not deemed necessary because of the focus of the intervention on improving organisational processes; individual patients will not be directly involved (IRB reference number: W16_271). Additionally, in the Netherlands, there is no need to obtain consent to use data from registries that do not contain patient-identifying information, as is the case in the NICE registry. The NICE foundation is officially registered according to the Dutch Personal Data Protection Act.
: Not applicable.
: The authors declare that they have no competing interests.
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