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dc.contributor.authorVincent, Britzer Paul
dc.contributor.authorRandhawa, Gurch
dc.contributor.authorCook, Erica Jane
dc.date.accessioned2020-08-12T09:24:04Z
dc.date.available2020-06-21T00:00:00Z
dc.date.available2020-08-12T09:24:04Z
dc.date.issued2020-06-21
dc.identifier.citationVincent BP, Randhawa G, Cook E (2020) 'Barriers towards organ donor registration and consent among people of Indian origin living globally: a systematic review and integrative synthesis - protocol', BMJ Open, 10 (6), pp.e035360.en_US
dc.identifier.issn2044-6055
dc.identifier.pmid32565460
dc.identifier.doi10.1136/bmjopen-2019-035360
dc.identifier.urihttp://hdl.handle.net/10547/624377
dc.description.abstractIntroduction The need for organs is comparatively higher among people of Indian origin due to the higher prevalence of end-stage organ failure. In spite of the higher need, they have a lower number of organ donors. Studies have been carried out among people of Indian origin living globally to understand the reasons for the low donation rate, but there has been no systematic review that has integrated all of these studies to synthesise the current literature. Therefore, the purpose of this review is to examine the barriers towards organ donor registration and consent among Indians living globally. Methods and analysis A systematic search will be conducted using the following relevant databases namely CINHAL, MEDLINE, PsycINFO, Scopus, Web of Science, PubMed Central, Global Health and Grey literature. Studies from 1994 that satisfy our inclusion criteria will be included. Two reviewers will conduct the screening, data extraction and quality assessment of the studies; in event of any disagreement between the two reviewers at any stage, the third reviewer will reconcile any disagreements and consensus will be made. Ethics and dissemination As this study includes only secondary data, ethical approval for secondary data usage has been sought. This study will use Preferred Reporting Items for Systematic Review and Meta-Analysis guidelines to report and the study outcomes will be disseminated through a relevant peer-review publication, related conferences and also to various non-governmental organisations globally which are working with this particular community; following which further research can be developed based on this evidence and also helps in building a culturally competent strategy. PROSPERO registration number CRD42019155274.en_US
dc.language.isoenen_US
dc.publisherBMJ Publishing Groupen_US
dc.relation.urlhttps://bmjopen.bmj.com/content/10/6/e035360en_US
dc.rightsGreen - can archive pre-print and post-print or publisher's version/PDF
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectprotocols and guidelinesen_US
dc.subjectmedical ethicsen_US
dc.subjectSubject Categories::C841 Health Psychologyen_US
dc.titleBarriers towards organ donor registration and consent among people of Indian origin living globally: a systematic review and integrative synthesis - protocolen_US
dc.typeArticleen_US
dc.identifier.eissn2044-6055
dc.contributor.departmentUniversity of Bedfordshireen_US
dc.identifier.journalBMJ Openen_US
dc.date.updated2020-08-12T09:21:07Z
dc.description.noteopen access


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