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dc.contributor.authorMcCall, Stephen J
dc.contributor.authorImran, Mahrukh
dc.contributor.authorHemkens, Lars G
dc.contributor.authorMc Cord, Kimberly
dc.contributor.authorKwakkenbos, Linda
dc.contributor.authorSampson, Margaret
dc.contributor.authorJawad, Sena
dc.contributor.authorZwarenstein, Merrick
dc.contributor.authorRelton, Clare
dc.contributor.authorLangan, Sinéad M
dc.contributor.authorMoher, David
dc.contributor.authorFröbert, Ole
dc.contributor.authorThombs, Brett D
dc.contributor.authorGale, Chris
dc.contributor.authorJuszczak, Edmund
dc.contributor.authorCONSORT Extension for Trials Conducted Using Cohorts and Routinely Collected Data Group
dc.date.accessioned2022-08-24T09:52:00Z
dc.date.available2022-08-24T09:52:00Z
dc.date.issued2022
dc.identifier.citationMcCall , S J , Imran , M , Hemkens , L G , Mc Cord , K , Kwakkenbos , L , Sampson , M , Jawad , S , Zwarenstein , M , Relton , C , Langan , S M , Moher , D , Fröbert , O , Thombs , B D , Gale , C , Juszczak , E & CONSORT Extension for Trials Conducted Using Cohorts and Routinely Collected Data Group 2022 , ' Reporting transparency and completeness in trials : Paper 4 - reporting of randomised controlled trials conducted using routinely collected electronic records - room for improvement ' , Journal of Clinical Epidemiology , vol. 141 , pp. 198-209 . https://doi.org/10.1016/j.jclinepi.2021.09.011en
dc.identifier.issn0895-4356
dc.identifier.otherPURE: 209925723
dc.identifier.otherPURE UUID: d3ba44d7-17d9-463b-8050-429508f33d7c
dc.identifier.otherPubMed: 34525409
dc.identifier.otherORCID: /0000-0003-0078-7010/work/104792452
dc.identifier.otherScopus: 85117769886
dc.identifier.urihttps://hdl.handle.net/2164/19101
dc.descriptionAcknowledgements This part of the project was funded by the National Institute for Health Research (NIHR) CTU Support Funding scheme - Supporting efficient/innovative delivery of NIHR research (PI Juszczak, Co-PI Gale, supported salary of SM). The views expressed are those of the author(s) and not necessarily those of the NIHR or the Department of Health and Social Care. The development of CONSORT-ROUTINE and the present study were funded by grants from the Canadian Institutes of Health Research (PI Thombs, #PJT-156172; PIs Thombs and Kwakkenbos, #PCS-161863) and from the United Kingdom National Institute of Health Research (NIHR) Clinical Trials Unit Support Funding. Dr. Langan was supported by a Wellcome Senior Clinical Fellowship in Science (205039/Z/16/Z). Dr. Gale was supported by the United Kingdom Medical Research Council through a Clinician Scientist Fellowship. Dr. Thombs was supported by a Fonds de recherche du Québec - Santé researcher salary award and a Tier 1 Canada Research Chair. Dr. Moher was supported by a University Research Chair (uOttawa).en
dc.format.extent12
dc.language.isoeng
dc.relation.ispartofJournal of Clinical Epidemiologyen
dc.rightsThis is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)en
dc.subjectCONSORT-ROUTINEen
dc.subjectExtensionen
dc.subjectRoutinelyen
dc.subjectCollecteden
dc.subjectHealthen
dc.subjectDataen
dc.subjectR Medicineen
dc.subjectWellcome Trusten
dc.subject205039/Z/16/Zen
dc.subjectNational Institute for Health Research (NIHR)en
dc.subject.lccRen
dc.titleReporting transparency and completeness in trials : Paper 4 - reporting of randomised controlled trials conducted using routinely collected electronic records - room for improvementen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Other Applied Health Sciencesen
dc.description.statusPeer revieweden
dc.description.versionPublisher PDFen
dc.identifier.doihttps://doi.org/10.1016/j.jclinepi.2021.09.011


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