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dc.contributor.authorMills, Katieen
dc.contributor.authorEmery, Jonen
dc.contributor.authorDennison, Beckyen
dc.contributor.authorRadford, Michaelen
dc.contributor.authorPannebakker, Merelen
dc.contributor.authorHall, Peren
dc.contributor.authorBurrows, Nigelen
dc.contributor.authorWilliams, Kateen
dc.contributor.authorSaunders, Catherineen
dc.contributor.authorMurchie, Peteren
dc.contributor.authorWalter, Fionaen
dc.date.accessioned2018-01-30T17:47:16Z
dc.date.available2018-01-30T17:47:16Z
dc.date.issued2017-11-28en
dc.identifier.issn2044-6055
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/271367
dc.description.abstractIntroduction Melanoma is the fifth commonest cancer in the UK. Incidence rates have quadrupled over the last 30 years and continue to rise, especially among younger people. As routine screening of the general population is not currently recommended in the UK, a focus on secondary prevention through early detection and prompt treatment in individuals at increased risk of melanoma could make an important contribution to improve melanoma outcomes. This paper describes the protocol for a phase II, multisite, randomised controlled trial, in the primary care setting, for patients at increased risk of melanoma. A skin self-monitoring smartphone ‘App’ was used to improve symptom appraisal and encourage help-seeking in primary care, thereby promoting early presentation with skin changes suspicious of melanoma. Methods and analysis We aim to recruit 200 participants from general practice waiting rooms in the East of England. Eligible patients are those identified at higher melanoma risk (using a real-time risk assessment tool), without a personal history of melanoma, aged 18 to 75 years. Participants will be invited to a primary care nurse consultation, and randomised to the Intervention group (standard written advice on skin cancer detection and sun protection, loading of a skin self-monitoring ‘App’ onto the participant’s smartphone, and instructions on use including self-monitoring reminders) or Control group (standard written advice alone). The primary outcomes are consultation rates for changes to a pigmented skin lesion, and the patient interval (time from first noticing a skin change to consultation). Secondary outcomes include patient sun-protection behaviours, psychosocial outcomes, and measures of trial feasibility and acceptability. Ethics and dissemination NHS ethical approval has been obtained from Cambridgeshire and Hertfordshire research ethics committee (REC reference 16/EE/0248). The findings from the MelaTools SSM Trial will be disseminated widely through peer-reviewed publications and scientific conferences. Trial registration number: ISCTRN registry, ISCTRN16061621
dc.description.sponsorshipThis work was supported by FMW’s Clinician Scientist award (RG 68235) from the National Institute for Health Research (NIHR). ... The paper also presents independent research funded/supported by the National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research & Care (CLAHRC) East of England, at Cambridgeshire and Peterborough NHS Foundation Trust.
dc.format.mediumElectronicen
dc.languageengen
dc.publisherBMJ Publishing Group
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectHumansen
dc.subjectMelanomaen
dc.subjectSelf Careen
dc.subjectLogistic Modelsen
dc.subjectResearch Designen
dc.subjectQuality of Lifeen
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectAgeden
dc.subjectMiddle Ageden
dc.subjectReferral and Consultationen
dc.subjectPrimary Health Careen
dc.subjectEnglanden
dc.subjectFemaleen
dc.subjectMaleen
dc.subjectYoung Adulten
dc.subjectMobile Applicationsen
dc.subjectSmartphoneen
dc.titleProtocol for the melatools skin self-monitoring trial: a phase II randomised controlled trial of an intervention for primary care patients at higher risk of melanoma.en
dc.typeArticle
prism.issueIdentifier11en
prism.publicationDate2017en
prism.publicationNameBMJ openen
prism.startingPagee017934
prism.volume7en
dc.identifier.doi10.17863/CAM.18351
dc.identifier.doi10.17863/CAM.18351
dc.identifier.doi10.17863/CAM.18351
dcterms.dateAccepted2017-10-31en
rioxxterms.versionofrecord10.1136/bmjopen-2017-017934en
rioxxterms.versionVoR*
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserveden
rioxxterms.licenseref.startdate2017-11-28en
dc.contributor.orcidMills, Katie [0000-0002-6563-2944]
dc.contributor.orcidEmery, Jon [0000-0002-5274-6336]
dc.contributor.orcidLantaff, Rebecca [0000-0002-0847-0723]
dc.contributor.orcidWilliams, Kate [0000-0002-6188-9363]
dc.contributor.orcidSaunders, Catherine [0000-0002-3127-3218]
dc.contributor.orcidMurchie, Peter [0000-0001-9968-5991]
dc.contributor.orcidWalter, Fiona [0000-0002-7191-6476]
dc.identifier.eissn2044-6055
rioxxterms.typeJournal Article/Reviewen
pubs.funder-project-idNational Institute for Health Research (NIHR-CS-012-030)


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International