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Authors
Anrys, Pauline
Strauven, Goedele
Roussel, Sandrine
Vande Ginste, Marie
De Lepeleire, Jan
Foulon, Veerle
Spinewine, Anne https://orcid.org/0000-0002-3836-2846
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Funding
Funding for this research was provided by:
National Institute for Health and Disability Insurance (B221100002)
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Article History
Received: 10 June 2019
Accepted: 1 October 2019
First Online: 11 December 2019
Ethics approval and consent to participate
: The COME-ON trial was approved by the Ethics Committee of UZ Leuven on November 12, 2014 (reference number s57145, ML11035). Furthermore, this study was also approved by the Belgian Privacy Commission on October 21, 2014 (Beraadslaging nr. 14/095, reference: SCSZ/14/084/174). All included NHRs or residents’ representatives provided their written informed consent before the beginning of the study. The director, coordinating physician, chief nurse, and pharmacist also provided written informed consent before the beginning of the study. Completion of the training questionnaire implied consent to participate; written information was provided at the start of the online questionnaire about the purpose of the questionnaire, the voluntary nature of participation and assurances that no individual data would be disclosed. Healthcare professionals gave oral consent for participation and audio-recording before starting the focus groups.
: Not applicable
: The authors declare that they have no competing interests.
