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Authors
van Houten, Miriam E.
Vloet, Lilian C. M.
Rikkert, Marcel G. M. Olde
van de Kerkhof-van Bon, Brigitte
de Rooij, Anneriek
Verhoeven, Marieke
Bil, Wilhelmina M. E.
Lucke, Jacinta A.
Schoon, Yvonne
Berben, Sivera A. A.
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Funding
Funding for this research was provided by:
the Dutch Ministry of Health, Welfare and Sport (PRJ 00697, PRJ 00697, PRJ 00697, PRJ 00697, PRJ 00697, PRJ 00697, PRJ 00697, PRJ 00697, PRJ 00697, PRJ 00697)
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Article History
Received: 29 January 2024
Accepted: 20 March 2024
First Online: 3 April 2024
Declarations
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: Potential respondents (healthcare professionals) received written information on the purpose of the study, data management, privacy aspects, and the required time investment according to the Medical Research with Human Subjects Law. After providing the study details, the professionals were asked to provide informed consent following the declaration of Helsinki. Due to the data collection during the Covid-19 period and potentially highly entrusted staff, we asked respondents for oral informed consent. Because no patients but only healthcare professionals were involved in the assessment of acceptability and appropriateness of the tool, and because the questionnaire did not pose any additional (mental) risk for these professionals, no formal approval of the ethics commission was deemed necessary according to the Medical Research with Human Subjects Law, and therefore approval was waived by the research group.
: Not applicable.
: The authors declare no competing interests.
