Hofstra, Emma http://orcid.org/0000-0003-4871-8997
Elfeddali, Iman
Metz, Margot
Bakker, Marjan
de Jong, Jacobus J.
van Nieuwenhuizen, Chijs
van der Feltz-Cornelis, Christina M.
Funding for this research was provided by:
ZonMw (537001002)
Article History
Received: 18 September 2019
Accepted: 24 October 2019
First Online: 19 November 2019
Ethics approval and consent to participate
: To protect vulnerable people with suicidal behavior, this study will be conducted according to the principles of the Declaration of Helsinki and in accordance with the Medical Research Involving Human Subjects Acts (WMO) and other guidelines, regulations, and acts. Our study protocol (version 3, 23 October 2017) and amendments (version 4, 10 September 2018; version 5, 21 March 2019) have been approved by the Medical Ethics Committee Brabant at 8 Nov 2017, 24 Oct 2018, and 25 March 2019 respectively (#NL6193502817/P1736). Eligible people registered in the monitoring system will be asked for written informed consent to participate. The information letter and informed consent form can be obtained via the authors and contains information about what participation in the study involves for participants, what is expected of participants if they participate, possible side effects and (dis)advantages and information regarding participation. After providing informed consent, participants will receive an email with a link to the questionnaires.
: Not applicable.
: The authors declare that they have no competing interests.