Kooijmans, Eline C. M. http://orcid.org/0000-0002-4776-5364
Hoogendijk, Emiel O.
Pokladníková, Jitka
Smalbil, Louk
Szczerbińska, Katarzyna
Barańska, Ilona
Ziuziakowska, Adrianna
Fialová, Daniela
Onder, Graziano
Declercq, Anja
Finne-Soveri, Harriet
Hoogendoorn, Mark
van Hout, Hein P. J.
Joling, Karlijn J.
Funding for this research was provided by:
Horizon 2020 Framework Programme (965341)
Seventh Framework Programme (305912)
Article History
Received: 12 June 2023
Accepted: 13 September 2023
First Online: 4 October 2023
Declarations
:
: None declared.
: The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request and with permission from the IBenC consortium.
: Ethical approval was obtained before the start of the IBenC study from authorized medical ethical committees in each of the participating countries. Belgium (Flanders): Commissie Medische Ethiek van de Universitair Medische Ziekenhuizen Katholieke Universiteit Leuven, No. ML10265; Finland: Tutkimuseettinen työryhmä, No. THL/796/6.02.01/ 533/2014; Germany: Ethikkommission des Institut für Psychologie und Arbeitswissenschaft der Technische Universtität Berlin, No. GH_01_20131022; Iceland: Vísindasiðanefnd, No. 13–176-S1; Italy: Comitato Etico Università Cattolica del Sacro Cuore, No. 2365/14; The Netherlands: Medical Ethics Review Committee VU University Medical Center, No. 2013.333.
: Informed consent was obtained from all study participants, except from routine care sites in Italy, Finland and one site in the Netherlands. In line with local regulations, informed consent from routine care clients was not necessarily required as these assessments were performed for clinical purposes by organizations’ own staff. Directly identifiable information of these clients was removed before transfer to the research teams, resulting in pseudonymized data.