Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/18568
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dc.contributor.authorBugge, Carolen_UK
dc.contributor.authorWilliams, Brianen_UK
dc.contributor.authorHagen, Suzanneen_UK
dc.contributor.authorLogan, Janeten_UK
dc.contributor.authorGlazener, Cathrynen_UK
dc.contributor.authorPringle, Stewarten_UK
dc.contributor.authorSinclair, Lesleyen_UK
dc.date.accessioned2018-04-26T03:38:00Z-
dc.date.available2018-04-26T03:38:00Z-
dc.date.issued2013-10en_UK
dc.identifier.other353en_UK
dc.identifier.urihttp://hdl.handle.net/1893/18568-
dc.description.abstractBackground: Current Medical Research Council (MRC) guidance on complex interventions advocates pilot trials and feasibility studies as part of a phased approach to the development, testing, and evaluation of healthcare interventions. In this paper we discuss the results of a recent feasibility study and pilot trial for a randomized controlled trial (RCT) of pelvic floor muscle training for prolapse (ClinicalTrials.gov: NCT01136889). The ways in which researchers decide to respond to the results of feasibility work may have significant repercussions for both the nature and degree of tension between internal and external validity in a definitive trial. Methods: We used methodological issues to classify and analyze the problems that arose in the feasibility study. Four centers participated with the aim of randomizing 50 women. Women were eligible if they had prolapse of any type, of stage I to IV, and had a pessary successfully fitted. Postal questionnaires were administered at baseline, 6 months, and 7 months post-randomization. After identifying problems arising within the pilot study we then sought to locate potential solutions that might minimize the trade-off between a subsequent explanatory versus pragmatic trial. Results: The feasibility study pointed to significant potential problems in relation to participant recruitment, features of the intervention, acceptability of the intervention to participants, and outcome measurement. Finding minimal evidence to support our decision-making regarding the transition from feasibility work to a trial, we developed a systematic process (A process for Decision-making after Pilot and feasibility Trials (ADePT)) which we subsequently used as a guide. The process sought to: 1) encourage the systematic identification and appraisal of problems and potential solutions; 2) improve the transparency of decision-making processes; and 3) reveal the tensions that exist between pragmatic and explanatory choices. Conclusions: We have developed a process that may aid researchers in their attempt to identify the most appropriate solutions to problems identified within future pilot and feasibility RCTs. The process includes three key steps: a decision about the type of problem, the identification of all solutions (whether addressed within the intervention, trial design or clinical context), and a systematic appraisal of these solutions.en_UK
dc.language.isoenen_UK
dc.publisherBioMed Central Ltden_UK
dc.relationBugge C, Williams B, Hagen S, Logan J, Glazener C, Pringle S & Sinclair L (2013) A process for Decision-making after Pilot and feasibility Trials (ADePT): Development following a feasibility study of a complex intervention for pelvic organ prolapse. Trials, 14 (1), Art. No.: 353. https://doi.org/10.1186/1745-6215-14-353en_UK
dc.rights© 2013 Bugge et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/2.0/en_UK
dc.subjectComplex interventionen_UK
dc.subjectPilot trialen_UK
dc.subjectFeasibility studyen_UK
dc.subjectMethodologyen_UK
dc.subjectPelvic organ prolapseen_UK
dc.titleA process for Decision-making after Pilot and feasibility Trials (ADePT): Development following a feasibility study of a complex intervention for pelvic organ prolapseen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1186/1745-6215-14-353en_UK
dc.identifier.pmid24160371en_UK
dc.citation.jtitleTrialsen_UK
dc.citation.issn1745-6215en_UK
dc.citation.volume14en_UK
dc.citation.issue1en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.author.emailcarol.bugge@stir.ac.uken_UK
dc.contributor.affiliationHealth Sciences Research - Stirling - LEGACYen_UK
dc.contributor.affiliationNMAHPen_UK
dc.contributor.affiliationGlasgow Caledonian Universityen_UK
dc.contributor.affiliationGlasgow Caledonian Universityen_UK
dc.contributor.affiliationUniversity of Aberdeenen_UK
dc.contributor.affiliationSouthern General Hospitalen_UK
dc.contributor.affiliationInstitute for Social Marketingen_UK
dc.identifier.isiWOS:000328748100002en_UK
dc.identifier.scopusid2-s2.0-84886156597en_UK
dc.identifier.wtid886597en_UK
dc.contributor.orcid0000-0002-4071-0803en_UK
dc.contributor.orcid0000-0003-0000-4354en_UK
dc.contributor.orcid0000-0002-2210-8181en_UK
dcterms.dateAccepted2013-10-31en_UK
dc.date.filedepositdate2014-02-07en_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorBugge, Carol|0000-0002-4071-0803en_UK
local.rioxx.authorWilliams, Brian|0000-0003-0000-4354en_UK
local.rioxx.authorHagen, Suzanne|en_UK
local.rioxx.authorLogan, Janet|en_UK
local.rioxx.authorGlazener, Cathryn|en_UK
local.rioxx.authorPringle, Stewart|en_UK
local.rioxx.authorSinclair, Lesley|0000-0002-2210-8181en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2014-02-07en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/2.0/|2014-02-07|en_UK
local.rioxx.filenameBugge et al. Trials 2013.pdfen_UK
local.rioxx.filecount1en_UK
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