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dc.date.accessioned2021-04-09T19:22:15Z
dc.date.available2021-04-09T19:22:15Z
dc.date.created2021-02-09T22:27:26Z
dc.date.issued2020
dc.identifier.citationTimmers, Marjolein van Dijck, Jeroen T. J. M. van Wijk, Roel P J Legrand, Valerie van Veen, Ernest Maas, Andrew I.R. Menon, David K Citerio, Giuseppe Stocchetti, Nino Kompanje, Erwin J.O. Andelic, Nada Andreassen, Lasse Anke, Audny Frisvold, Shirin Helseth, Eirik Røe, Cecilie Røise, Olav Skandsen, Toril Vik, Anne Åkerlund, Cecilia Amrein, Krisztina Antoni, Anna Audibert, Gerard Azouvi, Philippe Azzolini, Maria Luisa Bartels, Ronald Barzo, Pal Beauvais, Romuald Beer, Ronny Bellander, Bo-Michael Belli, Antonio Benali, Habib Berardino, Maurizio Beretta, Luigi Blaabjerg, Morten Bragge, Peter Brazinova, Alexandra Brinck, Vibeke Brooker, Joanne Brorsson, Camilla Buki, Andras Bullinger, Monika Cabeleira, Manuel Caccioppola, Alessio Calappi, Emiliana Calvi, Maria Rosa Cameron, Peter Lozano, Guillermo Carbayo Carbonara, Marco Cavallo, Simona . How do 66 European institutional review boards approve one protocol for an international prospective observational study on traumatic brain injury? Experiences from the CENTER-TBI study. BMC Medical Ethics. 2020, 21:36(1)
dc.identifier.urihttp://hdl.handle.net/10852/85116
dc.description.abstractBackground The European Union (EU) aims to optimize patient protection and efficiency of health-care research by harmonizing procedures across Member States. Nonetheless, further improvements are required to increase multicenter research efficiency. We investigated IRB procedures in a large prospective European multicenter study on traumatic brain injury (TBI), aiming to inform and stimulate initiatives to improve efficiency. Methods We reviewed relevant documents regarding IRB submission and IRB approval from European neurotrauma centers participating in the Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury (CENTER-TBI). Documents included detailed information on IRB procedures and the duration from IRB submission until approval(s). They were translated and analyzed to determine the level of harmonization of IRB procedures within Europe. Results From 18 countries, 66 centers provided the requested documents. The primary IRB review was conducted centrally (N = 11, 61%) or locally (N = 7, 39%) and primary IRB approval was obtained after one (N = 8, 44%), two (N = 6, 33%) or three (N = 4, 23%) review rounds with a median duration of respectively 50 and 98 days until primary IRB approval. Additional IRB approval was required in 55% of countries and could increase duration to 535 days. Total duration from submission until required IRB approval was obtained was 114 days (IQR 75–224) and appeared to be shorter after submission to local IRBs compared to central IRBs (50 vs. 138 days, p = 0.0074). Conclusion We found variation in IRB procedures between and within European countries. There were differences in submission and approval requirements, number of review rounds and total duration. Research collaborations could benefit from the implementation of more uniform legislation and regulation while acknowledging local cultural habits and moral values between countries.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleHow do 66 European institutional review boards approve one protocol for an international prospective observational study on traumatic brain injury? Experiences from the CENTER-TBI study
dc.typeJournal article
dc.creator.authorTimmers, Marjolein
dc.creator.authorvan Dijck, Jeroen T. J. M.
dc.creator.authorvan Wijk, Roel P J
dc.creator.authorLegrand, Valerie
dc.creator.authorvan Veen, Ernest
dc.creator.authorMaas, Andrew I.R.
dc.creator.authorMenon, David K
dc.creator.authorCiterio, Giuseppe
dc.creator.authorStocchetti, Nino
dc.creator.authorKompanje, Erwin J.O.
dc.creator.authorAndelic, Nada
dc.creator.authorAndreassen, Lasse
dc.creator.authorAnke, Audny
dc.creator.authorFrisvold, Shirin
dc.creator.authorHelseth, Eirik
dc.creator.authorRøe, Cecilie
dc.creator.authorRøise, Olav
dc.creator.authorSkandsen, Toril
dc.creator.authorVik, Anne
dc.creator.authorÅkerlund, Cecilia
dc.creator.authorAmrein, Krisztina
dc.creator.authorAntoni, Anna
dc.creator.authorAudibert, Gerard
dc.creator.authorAzouvi, Philippe
dc.creator.authorAzzolini, Maria Luisa
dc.creator.authorBartels, Ronald
dc.creator.authorBarzo, Pal
dc.creator.authorBeauvais, Romuald
dc.creator.authorBeer, Ronny
dc.creator.authorBellander, Bo-Michael
dc.creator.authorBelli, Antonio
dc.creator.authorBenali, Habib
dc.creator.authorBerardino, Maurizio
dc.creator.authorBeretta, Luigi
dc.creator.authorBlaabjerg, Morten
dc.creator.authorBragge, Peter
dc.creator.authorBrazinova, Alexandra
dc.creator.authorBrinck, Vibeke
dc.creator.authorBrooker, Joanne
dc.creator.authorBrorsson, Camilla
dc.creator.authorBuki, Andras
dc.creator.authorBullinger, Monika
dc.creator.authorCabeleira, Manuel
dc.creator.authorCaccioppola, Alessio
dc.creator.authorCalappi, Emiliana
dc.creator.authorCalvi, Maria Rosa
dc.creator.authorCameron, Peter
dc.creator.authorLozano, Guillermo Carbayo
dc.creator.authorCarbonara, Marco
dc.creator.authorCavallo, Simona
cristin.unitcode185,53,42,10
cristin.unitnameAvdeling for fysikalsk medisin og rehabilitering
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1888293
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=BMC Medical Ethics&rft.volume=21:36&rft.spage=&rft.date=2020
dc.identifier.jtitleBMC Medical Ethics
dc.identifier.volume21
dc.identifier.issue1
dc.identifier.pagecount14
dc.identifier.doihttps://doi.org/10.1186/s12910-020-00480-8
dc.identifier.urnURN:NBN:no-87758
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1472-6939
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/85116/1/How%2Bdo%2B66%2BEuropean%2Binstitutional.pdf
dc.type.versionPublishedVersion
cristin.articleid36
dc.relation.projectEU/602150
dc.relation.projectNFR/272789


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