Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/26132
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dc.contributor.authorLipman, Paula Darbyen_UK
dc.contributor.authorLoudon, Kirstyen_UK
dc.contributor.authorDluzak, Leonoraen_UK
dc.contributor.authorMoloney, Rachaelen_UK
dc.contributor.authorMessner, Donnaen_UK
dc.contributor.authorStoney, Catherine Men_UK
dc.date.accessioned2017-12-06T00:26:05Z-
dc.date.available2017-12-06T00:26:05Z-
dc.date.issued2017-11-10en_UK
dc.identifier.other532en_UK
dc.identifier.urihttp://hdl.handle.net/1893/26132-
dc.description.abstractBackground  There continues to be debate about what constitutes a pragmatic trial and how it is distinguished from more traditional explanatory trials. The NIH Pragmatic Trials Collaborative Project, which includes five trials and a coordinating unit, has adopted the Pragmatic-Explanatory Continuum Indicator Summary (PRECIS-2) instrument. The purpose of the study was to collect PRECIS-2 ratings at two points in time to assess whether the tool was sensitive to change in trial design, and to explore with investigators the rationale for rating shifts.  Methods  A mixed-methods design included sequential collection and analysis of quantitative data (PRECIS-2 ratings) and qualitative data. Ratings were collected at two annual, in-person project meetings, and subsequent interviews conducted with investigators were recorded, transcribed, and coded using NVivo 11 Pro for Windows. Rating shifts were coded as either (1) actual change (reflects a change in procedure or protocol), (2) primarily a rating shift reflecting rater variability, or (3) themes that reflect important concepts about the tool and/or pragmatic trial design.  Results  Based on PRECIS-2 ratings, each trial was highly pragmatic at the planning phase and remained so 1year later in the early phases of trial implementation. Over half of the 45 paired ratings for the nine PRECIS-2 domains indicated a rating change from Time 1 to Time 2 (N = 24, 53%). Of the 24 rating changes, only three represented a true change in the design of the trial. Analysis of rationales for rating shifts identified critical themes associated with the tool or pragmatic trial design more generally. Each trial contributed one or more relevant comments, with Eligibility, Flexibility of Adherence, and Follow-up each accounting for more than one.  Conclusions  PRECIS-2 has proved useful for “framing the conversation” about trial design among members of the Pragmatic Trials Collaborative Project. Our findings suggest that design elements assessed by the PRECIS-2 tool may represent mostly stable decisions. Overall, there has been a positive response to using PRECIS-2 to guide conversations around trial design, and the project’s focus on the use of the tool by this group of early adopters has provided valuable feedback to inform future trainings on the tool.en_UK
dc.language.isoenen_UK
dc.publisherBioMed Centralen_UK
dc.relationLipman PD, Loudon K, Dluzak L, Moloney R, Messner D & Stoney CM (2017) Framing the conversation: use of PRECIS-2 ratings to advance understanding of pragmatic trial design domains. Trials, 18 (1), Art. No.: 532. https://doi.org/10.1186/s13063-017-2267-yen_UK
dc.rights© The Author(s). 2017 This 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectPragmatic trialsen_UK
dc.subjectTrial designen_UK
dc.subjectEffectiveness trialsen_UK
dc.subjectMixed methodsen_UK
dc.subjectPRECIS-2 toolen_UK
dc.titleFraming the conversation: use of PRECIS-2 ratings to advance understanding of pragmatic trial design domainsen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1186/s13063-017-2267-yen_UK
dc.identifier.pmid29126437en_UK
dc.citation.jtitleTrialsen_UK
dc.citation.issn1745-6215en_UK
dc.citation.volume18en_UK
dc.citation.issue1en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.citation.date10/11/2017en_UK
dc.contributor.affiliationWestaten_UK
dc.contributor.affiliationHealth Sciences Stirlingen_UK
dc.contributor.affiliationWestaten_UK
dc.contributor.affiliationCenter for Medical Technology Policyen_UK
dc.contributor.affiliationNational Heart, Lung, and Blood Instituteen_UK
dc.contributor.affiliationNational Institutes of Health (US)en_UK
dc.identifier.isiWOS:000414909000003en_UK
dc.identifier.scopusid2-s2.0-85033362507en_UK
dc.identifier.wtid512061en_UK
dc.contributor.orcid0000-0002-4449-6226en_UK
dc.date.accepted2017-10-20en_UK
dcterms.dateAccepted2017-10-20en_UK
dc.date.filedepositdate2017-11-14en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorLipman, Paula Darby|en_UK
local.rioxx.authorLoudon, Kirsty|0000-0002-4449-6226en_UK
local.rioxx.authorDluzak, Leonora|en_UK
local.rioxx.authorMoloney, Rachael|en_UK
local.rioxx.authorMessner, Donna|en_UK
local.rioxx.authorStoney, Catherine M|en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2017-11-14en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2017-11-14|en_UK
local.rioxx.filenames13063-017-2267-y.pdfen_UK
local.rioxx.filecount1en_UK
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