Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34015
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dc.contributor.authorKong, Yee Wen-
dc.contributor.authorYuan, Cheng Yi-
dc.contributor.authorKiburg, Katerina-
dc.contributor.authorBrown, Katrin-
dc.contributor.authorTrawley, Steven-
dc.contributor.authorPartovi, Andi-
dc.contributor.authorRoem, Kerryn-
dc.contributor.authorHarrison, Natalie-
dc.contributor.authorFourlanos, Spiros-
dc.contributor.authorEkinci, Elif I-
dc.contributor.authorO'Neal, David N-
dc.date2023-
dc.date.accessioned2023-10-18T03:29:39Z-
dc.date.available2023-10-18T03:29:39Z-
dc.date.issued2023-10-09-
dc.identifier.citationPilot and Feasibility Studies 2023-10-09; 9(1)en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34015-
dc.description.abstractInsulin pump therapy (IPT) improves glucose control in people with type 1 diabetes (T1D) compared with multiple daily injections (MDI). However, their size, the tethered insulin infusion set, intrusiveness when operating the device and the need to disconnect during showering limit their acceptance to many who may benefit. The Omnipod DASH® Insulin Management System is a small waterproof tubeless device which is wirelessly controlled by a handheld device which may be an acceptable alternative. However, there are no randomised controlled trials focusing on the impact on user perceptions of tubeless insulin pump therapy. This pilot study aims to assess study feasibility and acceptability of patch pump therapy compared with usual care in adults with T1D in Australia to inform power calculations and progression to a large-scale multi-site randomised controlled study. A pilot multi-site parallel randomised controlled study will be conducted in sixty-four adults with T1D who are managed on MDI or IPT and self-monitoring with finger-stick blood glucose from four specialist diabetes centres in Victoria, Australia. Following carbohydrate counting education, participants will be randomised to use Omnipod DASH® System (Omnipod group) or continue usual care (usual care group) for 12 weeks, followed by a 12-week extension phase where all participants will use Omnipod DASH® System. The primary outcome measure is feasibility determined by study completion rates with a threshold of 0.80. Acceptability of the intervention (Omnipod DASH® System) will be assessed by the difference in Diabetes Technology Questionnaire 'current' (DTQ-current) score at 12 weeks post-randomisation compared to baseline. Secondary outcomes will include other measures of user acceptance, process outcomes, resource outcomes, participant-centred outcomes, healthcare professional perceptions and glycaemic outcomes. This pilot study will provide insights regarding the feasibility of the study design and the first data regarding user acceptance of insulin patch pump technology in Australian T1D adults. We anticipate that this study will provide information informing the design of a larger study evaluating the impact of patch pumps on subjective outcomes that are of significance to the person living with T1D. Australian New Zealand Clinical Trials Registry ( https://anzctr.org.au/ ) ACTRN12621001195842 (8th September 2021). Please refer to Additional file 1: Appendix 1 for full details.en_US
dc.language.isoeng-
dc.subjectInsulin pump therapyen_US
dc.subjectPatch pumpen_US
dc.subjectTreatment satisfactionen_US
dc.subjectType 1 diabetesen_US
dc.titleA pilot randomised controlled parallel arm trial evaluating treatment satisfaction with the Omnipod DASH® Insulin Management System compared with usual care in adults with type 1 diabetes in Australia: rationale, study design and methodologies.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitlePilot and Feasibility Studiesen_US
dc.identifier.affiliationDiabetes Technology Research Group, The University of Melbourne, Melbourne, VIC, Australia.;Department of Endocrinology and Diabetes, St Vincent's Hospital Melbourne, Melbourne, VIC, Australia.;Department of Medicine, The University of Melbourne, 4th Floor, Clinical Sciences Building, 29 Regent Street, Fitzroy, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Endocrinology and Diabetes, St Vincent's Hospital Melbourne, Melbourne, VIC, Australia.;Department of Medicine, The University of Melbourne, 4th Floor, Clinical Sciences Building, 29 Regent Street, Fitzroy, VIC, Australia.en_US
dc.identifier.affiliationCairnmillar Institute, Camberwell, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, The University of Melbourne, 4th Floor, Clinical Sciences Building, 29 Regent Street, Fitzroy, VIC, Australia.en_US
dc.identifier.affiliationKeylead Health, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationDiabetes Technology Research Group, The University of Melbourne, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationGeelong Endocrinology and Diabetes, Geelong, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Diabetes and Endocrinology, The Royal Melbourne Hospital, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, The University of Melbourne, 4th Floor, Clinical Sciences Building, 29 Regent Street, Fitzroy, VIC, Australia.;Department of Endocrinology, Austin Health, Melbourne, VIC, Australia.;The Australian Centre for Accelerating Diabetes Innovations (ACADI), The University of Melbourne, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationEndocrinologyen_US
dc.identifier.doi10.1186/s40814-023-01400-4en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-0870-4032en_US
dc.identifier.pubmedid37814352-
dc.description.volume9-
dc.description.issue1-
dc.description.startpage171-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptEndocrinology-
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