Beck, Denise Karin http://orcid.org/0000-0002-2083-1966
Tielen, Mirjam
Rechards, Marloes
Timman, Reinier
Boonstra, Charlotte
Versteegh, Josette
van de Wetering, Jacqueline
Zietse, Robert
van Gelder, Teun
Weimar, Willem
van Saase, Jan
van Busschbach, Jan
Massey, Emma Kay
Funding for this research was provided by:
Nierstichting (SWO16.11)
Article History
Received: 6 July 2020
Accepted: 3 August 2020
First Online: 28 August 2020
Ethics approval and consent to participate
: Study protocol approved by Medical Ethical Committee at the University Medical Center Rotterdam (MEC-2018-125). All participants receive written information on the study and time to consider participation. Since adolescents, adults and incapacitated patients are being included in the study, as well as important others, different participant information forms and informed consent forms are used per group. Written informed consent is obtained from both patients (≥16 years) and important others prior to participation. For patients between 12 and 15 years old, written informed consent will be obtained from both patients and the parents/guardians. From incapacitated participants, written informed consent is obtained from both patients and the legal representative.
: Not applicable.
: The authors declare that they have no competing interests.