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Authors
Bek, L. Martine http://orcid.org/0000-0001-8257-7070
Berentschot, Julia C.
Hellemons, Merel E.
Huijts, Susanne M.
Aerts, Joachim G. J. V.
van Bommel, Jasper
van Genderen, Michel E.
Gommers, Diederik A. M. P. J.
Ribbers, Gerard M.
Heijenbrok-Kal, Majanka H.
van den Berg-Emons, Rita J. G.
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Bek, L. Martine
Berentschot, Julia C.
Hellemons, Merel E.
Huijts, Susanne M.
Aerts, Joachim G. J. V.
Heijenbrok-Kal, Majanka H.
van den Berg-Emons, Rita J. G.
Ribbers, Gerard M.
van Bommel, Jasper
van Genderen, Michel E.
Gommers, Diederik A. M. P. J.
Ista, Erwin
van der Stoep, Robert
Osterthun, Rutger
Wijffels, Markus P. J. M.
Slaman, Jorrit
Visser, Marieke M.
Tazmi-Staal, Janette J.
Willems, Eva G.
Heller, Roxane
Gajadin, Shai A.
Blox, Wouter J. B.
Oswald, Laurien
Bindraban, Sieshem
Slingerland, Rob
van de Sande, Herbert J.
Kadir, Hawre
van Lanen, Marc
van Rossem, Ronald N.
van Loon-Kooij, Stephanie
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Funding
Funding for this research was provided by:
zonmw (10430022010026)
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Article History
Received: 12 July 2021
Accepted: 26 July 2021
First Online: 21 August 2021
Declarations
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: The study is performed in accordance with the Declaration of Helsinki. The Medical Ethics Committee of Erasmus MC approved the study (protocol number: MEC-2020-0487) on 23 June 2020. Approval was provided for all trial sites by this committee. Study information letters are provided to eligible patients and/or relatives by the treating physician at hospital discharge or as soon as possible thereafter by 1] treating physician at regular follow-up in hospital at 6 and 12 weeks; or 2] treating rehabilitation physician during inpatient medical rehabilitation; or 3] treating elderly care physician or research nurse in skilled nursing facility or sheltered care facility. In this information letter, the patient is asked to contact the researcher (via phone, email, or postal service) or participation is asked during regular follow-up in hospital or during inpatient medical rehabilitation or skilled nursing facility. All participants have a reflection time up to 1 week to ask questions about the study before they provide written informed consent to participate in the study, signed by the patient and researcher.
: Not applicable.
: The authors declare that they have no competing interests.
