Sökning: onr:"swepub:oai:DiVA.org:oru-94433" > Reporting Transpare...
Fältnamn | Indikatorer | Metadata |
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000 | 07579naa a2200565 4500 | |
001 | oai:DiVA.org:oru-94433 | |
003 | SwePub | |
008 | 210917s2022 | |||||||||||000 ||eng| | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-944332 URI |
024 | 7 | a https://doi.org/10.1016/j.jclinepi.2021.09.0122 DOI |
040 | a (SwePub)oru | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Cord, Kimberly A. Mc.u Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel, University of Basel, Basel, Switzerland4 aut |
245 | 1 0 | a Reporting Transparency and Completeness in Trials :b Paper 2 - Reporting of randomised trials using registries was often inadequate and hindered the interpretation of results |
264 | 1 | b Pergamon Press,c 2022 |
338 | a print2 rdacarrier | |
500 | a Funding agencies:Canadian Institutes of Health Research (CIHR) PJT-156172 PCS-161863 United Kingdom National Institute of Health Research (NIHR) Clinical Trials Unit Support FundingWellcome Senior Clinical Fellowship in Science 205039/Z/16/Z University Research ChairUnited Kingdom Medical Research Council through a Clinician Scientist FellowshipCanada Research Chairs | |
520 | a OBJECTIVE: Registries are important data sources for randomised controlled trials (RCTs), but reporting of how they are used may be inadequate. The objective was to describe the current adequacy of reporting of RCTs using registries.STUDY DESIGN AND SETTING: We used a database of trials using registries from a scoping review supporting the development of the 2021 CONSORT extension for Trials Conducted Using Cohorts and Routinely Collected Data (CONSORT-ROUTINE). Reporting completeness of 13 CONSORT-ROUTINE items was assessed.RESULTS: We assessed reports of 47 RCTs that used a registry, published between 2011 and 2018. Of the 13 CONSORT-ROUTINE items, 6 were adequately reported in at least half of reports (2 in at least 80%). The 7 other items were related to routinely collected data source eligibility (32% adequate), data linkage (8% adequate), validation and completeness of data used for outcome assessment (8% adequate), validation and completeness of data used for participant recruitment (0% adequate), participant flow (9% adequate), registry funding (6% adequate) and interpretation of results in consideration of registry use (25% adequate).CONCLUSION: Reporting of trials using registries was often poor, particularly details on data linkage and quality. Better reporting is needed for appropriate interpretation of the results of these trials. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Hälsovetenskapx Hälso- och sjukvårdsorganisation, hälsopolitik och hälsoekonomi0 (SwePub)303012 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Health Sciencesx Health Care Service and Management, Health Policy and Services and Health Economy0 (SwePub)303012 hsv//eng |
653 | a CONSORT | |
653 | a CONSORT-ROUTINE | |
653 | a randomised controlled trials | |
653 | a registries | |
653 | a reporting guideline | |
653 | a routinely collected data | |
700 | 1 | a Imran, Mahrukhu Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Quebec, Canada4 aut |
700 | 1 | a Rice, Danielle B.u Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Quebec, Canada; Department of Psychology, McGill University, Montreal, Quebec, Canada4 aut |
700 | 1 | a McCall, Stephen J.u National Perinatal Epidemiology Unit Clinical Trials Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom; Center for Research on Population and Health, Faculty of Health Sciences, American University of Beirut, Ras Beirut, Lebanon4 aut |
700 | 1 | a Kwakkenbos, Lindau Behavioural Science Institute, Clinical Psychology, Radboud University, Nijmegen, the Netherlands4 aut |
700 | 1 | a Sampson, Margaretu Library Services, Children's Hospital of Eastern Ontario, Ottawa, Canada4 aut |
700 | 1 | a Fröbert, Ole,d 1964-u Örebro universitet,Institutionen för medicinska vetenskaper,Department of Cardiology4 aut0 (Swepub:oru)oft |
700 | 1 | a Gale, Chrisu Neonatal Medicine, School of Public Health, Faculty of Medicine, Imperial College London, London, UK4 aut |
700 | 1 | a Langan, Sinéad M.u Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK4 aut |
700 | 1 | a Moher, Davidu Centre for Journalology, Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada4 aut |
700 | 1 | a Relton, Clareu Centre for Clinical Trials and Methodology, Barts Institute of Population Health Science, Queen Mary University, London, UK4 aut |
700 | 1 | a Zwarenstein, Merricku Centre for Studies in Family Medicine, Department of Family Medicine, Schulich School of Medicine & Dentistry, Western University, London, Ontario, Canada; Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada4 aut |
700 | 1 | a Juszczak, Edmundu National Perinatal Epidemiology Unit Clinical Trials Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom; Nottingham Clinical Trials Unit, University of Nottingham, University Park, Nottingham, United Kingdom4 aut |
700 | 1 | a Thombs, Brett D.u Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Quebec, Canada; Department of Psychology, McGill University, Montreal, Quebec, Canada.; Department of Psychiatry, McGill University, Montreal, Quebec, Canada; Departments of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec, Canada; Department of Medicine, McGill University, Montreal, Quebec, Canada.; Department of Educational and Counselling Psychology, McGill University, Montreal, Quebec, Canada; Biomedical Ethics Unit, McGill University, Montreal, Quebec, Canada4 aut |
700 | 1 | a Hemkens, Lars G.u Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel, University of Basel, Basel, Switzerland; Meta-Research Innovation Center Berlin (METRIC-B), Berlin Institute of Health, Berlin, Germany; Meta-Research Innovation Center at Stanford (METRICS), Stanford University, Stanford, California, USA4 aut |
700 | 1 | a CONSORT Extension for Trials Conducted Using Cohorts and Routinely Collected Data Group, -u Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel, University of Basel, Basel, Switzerland; Meta-Research Innovation Center Berlin (METRIC-B), Berlin Institute of Health, Berlin, Germany; Meta-Research Innovation Center at Stanford (METRICS), Stanford University, Stanford, California, USA4 ctb |
710 | 2 | a Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel, University of Basel, Basel, Switzerlandb Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Quebec, Canada4 org |
773 | 0 | t Journal of Clinical Epidemiologyd : Pergamon Pressg 141, s. 175-186q 141<175-186x 0895-4356x 1878-5921 |
856 | 4 | u https://doi.org/10.1016/j.jclinepi.2021.09.012y Fulltext |
856 | 4 | u http://www.jclinepi.com/article/S0895435621002924/pdf |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-94433 |
856 | 4 8 | u https://doi.org/10.1016/j.jclinepi.2021.09.012 |
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