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dc.contributor.authorByrne, Molly
dc.contributor.authorO’Connell, Anthony
dc.contributor.authorEgan, Aoife M.
dc.contributor.authorDinneen, Sean F.
dc.contributor.authorHynes, Lisa
dc.contributor.authorO’Hara, Mary Clare
dc.contributor.authorHolt, Richard I. G.
dc.contributor.authorWillaing, Ingrid
dc.contributor.authorVallis, Michael
dc.contributor.authorHendrieckx, Christel
dc.contributor.authorCoyne, Imelda
dc.date.accessioned2018-09-20T16:02:17Z
dc.date.available2018-09-20T16:02:17Z
dc.date.issued2017-12-01
dc.identifier.citationByrne, Molly; O’Connell, Anthony; Egan, Aoife M. Dinneen, Sean F.; Hynes, Lisa; O’Hara, Mary Clare; Holt, Richard I. G.; Willaing, Ingrid; Vallis, Michael; Hendrieckx, Christel; Coyne, Imelda (2017). A core outcomes set for clinical trials of interventions for young adults with type 1 diabetes: an international, multi-perspective delphi consensus study. Trials 18 ,
dc.identifier.issn1745-6215
dc.identifier.urihttp://hdl.handle.net/10379/10634
dc.description.abstractBackground: Achieving consensus from a range of relevant stakeholders about an agreed set of core outcomes to be measured and reported as a minimum in clinical trials has the potential to enhance evidence synthesis and make findings more relevant and applicable. Intervention research to improve outcomes for young adults with type 1 diabetes (T1DM) is hampered by inconsistent use of outcome measures. This population frequently struggles to manage their condition and reports suboptimal clinical outcomes. Our aim was to conduct an international, e-Delphi consensus study to identify a core outcome set (COS) that key stakeholders (young adults with T1DM, diabetes health professionals, diabetes researchers and diabetes policy makers) consider as essential outcomes for future intervention research. Methods: Using a list of 87 outcomes generated from a published systematic review, we administered two online surveys to a sample of international key stakeholders. Participants in the first survey (survey 1; n = 132) and the second survey (survey 2; n = 81) rated the importance of the outcomes. Survey 2 participants received information on total mean rating for each outcome and a reminder of their personal outcome ratings from Survey 1. Survey 2 results were discussed at a consensus meeting and participants (n = 12: three young adults with T1DM, four diabetes health professionals, four diabetes researchers and one diabetes policy maker) voted on outcomes. Final core outcomes were included provided that 70% of consensus group participants voted for their inclusion. Results: Eight core outcomes were agreed for inclusion in the final COS: measures of diabetes-related stress; diabetes-related quality of life; number of severe hypoglycaemic events; self-management behaviour; number of instances of diabetic ketoacidosis (DKA); objectively measured glycated haemoglobin (HbA1C); level of clinic engagement; and perceived level of control over diabetes. Conclusions: This study is the first to identify a COS for inclusion in future intervention trials to improve outcomes for young adults with T1DM. Use of this COS will improve the quality of future research and increase opportunities for evidence synthesis. Future research is necessary to identify the most robust outcome measure instruments.
dc.publisherSpringer Nature
dc.relation.ispartofTrials
dc.subjectclinical diabetes
dc.subjecthealthcare delivery
dc.subjecttype 1 diabetes
dc.subjectyoung adults
dc.subjectinterventions
dc.subjectcore outcome set
dc.subjectself-management
dc.subjectrandomised controlled trials
dc.subjectpeople
dc.subjectcare
dc.titleA core outcomes set for clinical trials of interventions for young adults with type 1 diabetes: an international, multi-perspective delphi consensus study
dc.typeArticle
dc.identifier.doi10.1186/s13063-017-2364-y
dc.local.publishedsourcehttps://trialsjournal.biomedcentral.com/track/pdf/10.1186/s13063-017-2364-y?site=trialsjournal.biomedcentral.com
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