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Authors
Mulder, Frederike E. C. M. https://orcid.org/0000-0001-9307-1198
Witlox, M. Adhiambo
Dirksen, Carmen D.
de Witte, Pieter Bas
de Vos-Jakobs, Suzanne
Ham, Arno M. ten
Witbreuk, Melinda M. E. H.
Sakkers, Ralph
Drongelen, Magritha M. H. P. Foreman-van
Robben, Simon G. F.
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van Bergen, Christiaan J. A.
Besselaar, Arnold T.
Boot, Marieke
Burger, Bart J.
van Douveren, Florens Q. M. P.
van Gelder, J. H.
Hartog, Yvon M.den
Oost, Iris Koenraadt-van
van Linge, Joost H.
Maathuis, Patrick G. M.
Moerman, Sophie
Pereboom, Renske M.
Staal, Heleen M.
van der Steen, M. C.
Tolk, Jaap J.
Vergroesen, Diederik A.
Zeegers, A. V. C. M.
Mathijssen, Nina M. C.
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Funding
Funding for this research was provided by:
ZonMw (852002129)
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Article History
Received: 30 November 2022
Accepted: 13 April 2023
First Online: 29 April 2023
Declarations
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: All procedures performed in studies involving human participants will be in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The TRAM-Trial was approved by the Medical Ethics Committee of Maastricht University Medical Center + (MUMC +) and Maastricht University, the Netherlands (METC 21–036). Written informed consent of the infant will be obtained from both parents/caregivers. Additionally, informed consent of one parent/caregiver will be obtained from the parent/caregiver who will fill in the questionnaires.
: Not applicable.
: The authors declare that they have no competing interests.
