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dc.contributor.authorParry, Monica
dc.contributor.authorCeroni, Tina
dc.contributor.authorWells, David
dc.contributor.authorRichards, Dawn P.
dc.contributor.authorApril, Katrine Toupin
dc.contributor.authorAnsari, Hafsa
dc.contributor.authorBjørnnes, Ann Kristin
dc.contributor.authorBurnside, H
dc.contributor.authorCavallo, Sabrina
dc.contributor.authorDay, Andrew
dc.contributor.authorA, Ellis
dc.contributor.authorFeldman, Debbie
dc.contributor.authorGilron, Ian
dc.contributor.authorNajam, Adhiyat
dc.contributor.authorZulfiqar, Zoya
dc.contributor.authorMarlin, Susan
dc.coverage.spatialCanadaen_US
dc.date.accessioned2022-08-08T07:49:05Z
dc.date.available2022-08-08T07:49:05Z
dc.date.created2022-02-25T16:01:53Z
dc.date.issued2022-02-21
dc.identifier.issn2044-6055
dc.identifier.urihttps://hdl.handle.net/11250/3010520
dc.description.abstractIntroduction: Building capacity to improve sex/gender knowledge and strengthen patient engagement in clinical trials requires training and support. The overall goal of this 2-year project is to refine, translate and evaluate two web-based open-access patient and investigator decision aids aimed to improve patient engagement partnerships in clinical trials. Methods and analysis: Two decision aids were designed in Phase 1 of this programme of research and this protocol describes a subsequent sequential phased approach to refine/translate (Phase 2A) and conduct alpha/usability (Phase 2B) and beta/field (Phase 3) testing. Decision aid development is guided by the International Patient Decision Aid Standards, User-Centred Design, Ottawa Decision-Support Framework and the Ottawa Model of Research Use. We have integrated patient-oriented research methods by engaging patient partners across all phases of our programme of research. Decision aids will first be refined and then translated to French (Phase 2A). Eight iterative cycles of semistructured interviews with 40 participants (20 patient partners and 20 investigators) will be conducted to determine usability (Phase 2B). A pragmatic pre/post pilot study design will then be implemented for field/beta testing using another purposive sample of 80 English-speaking and French-speaking participants (40 patients and 40 investigators). The samples are purposive to ensure an equal representation of English-speaking and French-speaking participants and an equal representation of men and women. Since sex and/or gender differences in utilisation and effectiveness of decision aids have not been previously reported, Phase 3 outcomes will be reported for the total sample and separately for men and women.en_US
dc.description.sponsorshipThis work was supported by the Canadian Institute of Health Research Project Grant Fall 2019 and Spring 2020 (CIHR; 436272).en_US
dc.language.isoengen_US
dc.publisherBMJ Publishing Groupen_US
dc.relation.ispartofseriesBMJ Open;Volume 12, Issue 2
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.subjectPatient engagement partnershipsen_US
dc.subjectPatient aidsen_US
dc.subjectGender knowledgeen_US
dc.subjectClinical trialsen_US
dc.titlePatient engagement partnerships in clinical trials (PEP-CT): protocol for the systematic development and testing of patient partner and investigator decision aidsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© Author(s) (or their employer(s)) 2022en_US
dc.source.articlenumbere060267en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doihttp://dx.doi.org/10.1136/bmjopen-2021-060267
dc.identifier.cristin2005608
dc.source.journalBMJ Openen_US
dc.source.volume12en_US
dc.source.issue2en_US
dc.source.pagenumber1-7en_US
dc.relation.projectCanadian Institute of Health Research: 436272en_US


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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