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dc.contributor.authorBullen, James
dc.contributor.authorNickel, Brooke
dc.contributor.authorMcCaffery, Kirsten
dc.contributor.authorWilt, Timothy J.
dc.contributor.authorSmith, Jenna
dc.contributor.authorBoroumand, Farzaneh
dc.contributor.authorParker, Lisa
dc.contributor.authorMillar, Jeremy
dc.contributor.authorBrodersen, John
dc.contributor.authorDahm, Philipp
dc.contributor.authorDelahunt, Brett
dc.contributor.authorVarma, Murali
dc.contributor.authorGlasziou, Paul
dc.contributor.authorWarden, Andrew
dc.contributor.authorDiller, Lawrence
dc.contributor.authorBillington, Larry
dc.contributor.authorvan Rensburg, Christo
dc.contributor.authorBell, Katy
dc.date.accessioned2024-11-18T13:06:20Z
dc.date.available2024-11-18T13:06:20Z
dc.date.issued2024-08-09
dc.description.abstractIntroduction - Many types of prostate cancer present minimal risk to a man’s lifespan or well-being, but existing terminology makes it difficult for men to distinguish these from high-risk prostate cancers. This study aims to explore whether using an alternative label for low-risk prostate cancer influences management choice and anxiety levels among Australian men and their partners.<p> <p>Methods and analysis - We will run two separate studies for Australian men and Australian women with a male partner. Both studies are between-subjects factorial (3×2) randomised online hypothetical experiments. Following consent, eligible participants will be randomised 1:1:1 to three labels: ‘low-risk prostate cancer, Gleason Group 1’, ‘low-risk prostate neoplasm’ or ‘low-risk prostate lesion’. Participants will then undergo a second randomisation step with 1:1 allocation to the provision of detailed information on the benefits and harms of different management choices versus the provision of less detailed information about management choices. The required sample sizes are 1290 men and 1410 women. The primary outcome is the participant choice of their preferred management strategy: no immediate treatment (prostate-specific antigen (PSA)-based monitoring or active surveillance using PSA, MRI, biopsy with delayed treatment for disease progression) versus immediate treatment (prostatectomy or radiation therapy). Secondary outcomes include preferred management choice (from the four options listed above), diagnosis anxiety, management choice anxiety and management choice at a later time point (for participants who initially choose a monitoring strategy).<p> <p>Ethics and dissemination Ethics approval has been received from The University of Sydney Human Research Ethics Committee (2023/572). The results of the study will be published in a peer-reviewed medical journal and a plain language summary of the findings will be shared on the Wiser Healthcare publications page http://www.wiserhealthcare.org.au/category/publications/<p> <p>Trial registration numbers Australian New Zealand Clinical Trials Registry (ID 386701 and 386889).en_US
dc.identifier.citationBullen, Nickel, McCaffery, Wilt, Smith, Boroumand, Parker, Millar, Brodersen, Dahm, Delahunt, Varma, Glasziou, Warden, Diller, Billington, van Rensburg, Bell. Impact of the diagnostic label for a low-risk prostate lesion: protocol for two online factorial randomised experiments. BMJ Open. 2024;14(8):e085947
dc.identifier.cristinIDFRIDAID 2308819
dc.identifier.doi10.1136/bmjopen-2024-085947
dc.identifier.issn2044-6055
dc.identifier.urihttps://hdl.handle.net/10037/35745
dc.language.isoengen_US
dc.publisherBMJ Publishing Groupen_US
dc.relation.journalBMJ Open
dc.rights.holderCopyright 2024 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleImpact of the diagnostic label for a low-risk prostate lesion: protocol for two online factorial randomised experimentsen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution 4.0 International (CC BY 4.0)