Gerrits, Reinie G. https://orcid.org/0000-0001-8030-2882
Mulyanto, Joko
Wammes, Joost D.
van den Berg, Michael J.
Klazinga, Niek S.
Kringos, Dionne S.
Funding for this research was provided by:
ZonMw (445001003)
Article History
Received: 27 February 2020
Accepted: 4 August 2020
First Online: 3 September 2020
Ethics approval and consent to participate
: Ethical approval was deemed unnecessary by the study’s affiliated protocols (Medical Research Act with People [Wet medisch-wetenschappelijk onderzoek met mensen (WMO) [Dutch]], in BWBR0009408, W.a.S. Ministry of Health, Editor. 1998: Hague, Netherlands). A waiver for ethical approval was therefore obtained for this study from the Medical Ethics Review Committee at Amsterdam UMC. Survey participants provided written consent to participate at the start of the survey. Interview and focus group participants provided verbal consent at the start of all interviews and focus groups. Verbal consent was considered adequate as no human data was retained. To assure voluntary participation, informed consent was reiterated at the start of each focus group and recorded.
: Not applicable.
: The authors declare that they have no competing interests.