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dc.contributor.authorHarris, Janeten_US
dc.contributor.authorGraue, Mariten_US
dc.contributor.authorDunning, Trishaen_US
dc.contributor.authorHaltbakk, Johannesen_US
dc.contributor.authorAustrheim, Gunhilden_US
dc.contributor.authorSkille, Ninaen_US
dc.contributor.authorRokne, Beriten_US
dc.contributor.authorKirkevold, Mariten_US
dc.date.accessioned2016-08-24T07:56:15Z
dc.date.available2016-08-24T07:56:15Z
dc.date.issued2015-11-04
dc.PublishedSystematic Reviews 2015, 4:146eng
dc.identifier.issn2046-4053
dc.identifier.urihttps://hdl.handle.net/1956/12672
dc.description.abstractBackground: Patient and public involvement in diabetes research is now actively encouraged in different countries because it is believed that involving people with experience of the condition will improve the quality and relevance of the research. However, reviews of patient involvement have noted that inadequate resources, patients’ and communities’ lack of research knowledge, and researchers’ lack of skills to involve patients and communities in research may present significant contextual barriers. Little is known about the extent of patient/community involvement in designing or delivering interventions for people with diabetes. A realist review of involvement will contribute to assessing when, how and why involvement works, or does not work, to produce better diabetes interventions. Methods/design: This protocol outlines the process for conducting a realist review to map how patients and the public have been involved in diabetes research to date. The review questions ask the following: How have people with diabetes and the wider community been involved in diabetes research? What are the characteristics of the process that appear to explain the relative success or failure of involvement? How has involvement (or lack of involvement) in diabetes research influenced the development and conduct of diabetes research? The degree of support in the surrounding context will be assessed alongside the ways in which people interact in different settings to identify patterns of interaction between context, mechanisms and outcomes in different research projects. The level and extent of the involvement will be described for each stage of the research project. The descriptions will be critically reviewed by the people with diabetes on our review team. In addition, researchers and patients in diabetes research will be asked to comment. Information from researcher-patient experiences and documents will be compared to theories of involvement across a range of disciplines to create a mid-range theory describing how involvement (or lack of involvement) in diabetes research influences the development and conduct of diabetes research.en_US
dc.language.isoengeng
dc.publisherBioMed Centraleng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/eng
dc.subjectDiabetes mellituseng
dc.subjectHealth services researcheng
dc.subjectConsumer participationeng
dc.subjectPatient participationeng
dc.subjectCommunity-based participatory researcheng
dc.subjectRealist revieweng
dc.titleInvolving people with diabetes and the wider community in diabetes research: a realist review protocolen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2016-02-26T11:28:38Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright Harris et al.
dc.identifier.doihttps://doi.org/10.1186/s13643-015-0127-y
dc.identifier.cristin1314891


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