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Authors
de Best, Pauline A.
Broekhuizen, H.
Sikkema, R. S.
Koopmans, M. P. G.
Timen, A.
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Funding
Funding for this research was provided by:
Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWA.1160.1S.210)
Wageningen University and Research (WUR WASS 21-040)
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Article History
Received: 26 February 2024
Accepted: 20 January 2025
First Online: 24 January 2025
Change Date: 10 July 2025
Change Type: Update
Change Details: This article has been updated to amend the license information.
Declarations
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: All methods were carried out in accordance with relevant guidelines and regulations for human subjects research, European ethics requirements and best practices. The Centre for Clinical Expertise at the RIVM (Dutch National Institute for Public Health and the Environment) concluded that the protocol was not subject Dutch law for Medical Research Involving Human Subjects (WMO) or with the EU Clinical Trial Directive (2001/20/EC) and therefore concluded approval in advance by an ethical research committee or institutional review board was deemed unnecessary by current national and European legislation (Ref. LCI-662). Permission and informed consent for recording of the interviews, and analysis of the responses, with the aim of publishing a research manuscript, was obtained from each participant at the start of the interview.
: Not applicable.
: The authors declare no competing interests.
