A novel design process for selection of attributes for inclusion in discrete choice experiments: case study exploring variation in clinical decision-making about thrombolysis in the treatment of acute ischaemic stroke

dc.contributor.authorDe Brun, Aoife
dc.contributor.authorFlynn, Darren
dc.contributor.authorTernent, Laura
dc.contributor.authorPrice, Christopher I
dc.contributor.authorRodgers, Helen
dc.contributor.authorFord, Gary A
dc.contributor.authorRudd, Matthew
dc.contributor.authorLancsar, Emily
dc.contributor.authorSimpson, Stephen
dc.contributor.authorTeah, John
dc.contributor.authorThomson, Richard
dc.date.accessioned2021-10-15T02:42:34Z
dc.date.available2021-10-15T02:42:34Z
dc.date.issued2018
dc.date.updated2020-11-23T11:30:32Z
dc.description.abstractA discrete choice experiment (DCE) is a method used to elicit participants’ preferences and the relative importance of different attributes and levels within a decision-making process. DCEs have become popular in healthcare; however, approaches to identify the attributes/levels influencing a decision of interest and to selection methods for their inclusion in a DCE are under-reported. Our objectives were: to explore the development process used to select/present attributes/levels from the identified range that may be influential; to describe a systematic and rigorous development process for design of a DCE in the context of thrombolytic therapy for acute stroke; and, to discuss the advantages of our five-stage approach to enhance current guidance for developing DCEs. A five-stage DCE development process was undertaken. Methods employed included literature review, qualitative analysis of interview and ethnographic data, expert panel discussions, a quantitative structured prioritisation (ranking) exercise and pilot testing of the DCE using a ‘think aloud’ approach. The five-stage process reported helped to reduce the list of 22 initial patient-related factors to a final set of nine variable factors and six fixed factors for inclusion in a testable DCE using a vignette model of presentation. In order for the data and conclusions generated by DCEs to be deemed valid, it is crucial that the methods of design and development are documented and reported. This paper has detailed a rigorous and systematic approach to DCE development which may be useful to researchers seeking to establish methods for reducing and prioritising attributes for inclusion in future DCEs.en_AU
dc.description.sponsorshipFinancial support for this study was provided entirely by a grant from the National Institute for Health Research (NIHR) Health Services and Delivery Research Programme (project number: 12/5001/45).en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1472-6963en_AU
dc.identifier.urihttp://hdl.handle.net/1885/250872
dc.language.isoen_AUen_AU
dc.provenanceThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.en_AU
dc.publisherBioMed Centralen_AU
dc.rights© The Author(s). 2018en_AU
dc.rights.licenseCreative Commons License (Attribution 4.0 International)en_AU
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_AU
dc.sourceBMC Health Services Researchen_AU
dc.source.urihttp://dx.doi.org/10.1186/s12913-018-3305-5en_AU
dc.subjectDiscrete choice experimenten_AU
dc.subjectIntravenous thrombolysisen_AU
dc.subjectClinical decision-makingen_AU
dc.subjectAcute ischaemic strokeen_AU
dc.subjectDesign processen_AU
dc.subjectMethodologyen_AU
dc.subjectPatient vignettesen_AU
dc.titleA novel design process for selection of attributes for inclusion in discrete choice experiments: case study exploring variation in clinical decision-making about thrombolysis in the treatment of acute ischaemic strokeen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue1en_AU
local.bibliographicCitation.lastpage14en_AU
local.bibliographicCitation.startpage1en_AU
local.contributor.affiliationDe Brun, Aoife, Newcastle Universityen_AU
local.contributor.affiliationFlynn, Darren, Newcastle Universityen_AU
local.contributor.affiliationTernent, Laura, Newcastle Universityen_AU
local.contributor.affiliationPrice, Christopher I, NIHR Newcastle Biomedical Research Centreen_AU
local.contributor.affiliationRodgers, Helen, Newcastle Universityen_AU
local.contributor.affiliationFord, Gary A, Newcastle Universityen_AU
local.contributor.affiliationRudd, Matthew, Newcastle Universityen_AU
local.contributor.affiliationLancsar, Emily, College of Health and Medicine, ANUen_AU
local.contributor.affiliationSimpson, Stephen, The Stroke Associationen_AU
local.contributor.affiliationTeah, John, The Stroke Associationen_AU
local.contributor.affiliationThomson, Richard, Newcastle Universityen_AU
local.contributor.authoruidLancsar, Emily, u3594049en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor111708 - Health and Community Servicesen_AU
local.identifier.absfor110202 - Haematologyen_AU
local.identifier.absfor110321 - Rehabilitation and Therapy (excl. Physiotherapy)en_AU
local.identifier.ariespublicationu6378665xPUB7en_AU
local.identifier.citationvolume18en_AU
local.identifier.scopusID2-s2.0-85048884511
local.publisher.urlhttp://www.biomedcentral.com/en_AU
local.type.statusPublished Versionen_AU

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