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dc.contributor.authorMcHale, Calum Thomas
dc.contributor.authorCruickshank, Susanne
dc.contributor.authorBrown, Tamara
dc.contributor.authorTorrens, Claire
dc.contributor.authorArmes, Jo
dc.contributor.authorFenlon, Deborah
dc.contributor.authorBanks, Elspeth
dc.contributor.authorKelsey, Tom
dc.contributor.authorHumphris, Gerald Michael
dc.date.accessioned2024-01-08T12:30:07Z
dc.date.available2024-01-08T12:30:07Z
dc.date.issued2024-01-08
dc.identifier298080088
dc.identifier9927a2b5-4979-404c-a6ad-9806210512b6
dc.identifier85181940426
dc.identifier.citationMcHale , C T , Cruickshank , S , Brown , T , Torrens , C , Armes , J , Fenlon , D , Banks , E , Kelsey , T & Humphris , G M 2024 , ' Mini-AFTERc: a controlled pilot trial of a nurse-led psychological intervention for fear of breast cancer recurrence ' , Pilot and Feasibility Studies , vol. 10 , 3 . https://doi.org/10.1186/s40814-023-01431-xen
dc.identifier.issn2055-5784
dc.identifier.otherORCID: /0000-0002-4601-8834/work/150659716
dc.identifier.otherORCID: /0000-0002-8091-1458/work/150661431
dc.identifier.urihttps://hdl.handle.net/10023/28967
dc.descriptionFunding: The study was funded by the Chief Scientist Ofce (CSO), which is part of the Scottish Government Health Directorates (reference: HIPS/17/57).en
dc.description.abstractObjectives   To determine the feasibility and acceptability of implementing the Mini-AFTERc intervention. Design   Non-randomised cluster-controlled pilot trial. Setting  Four NHS out-patient breast cancer centres in Scotland. Participants  Ninety-two women who had successfully completed primary treatment for breast cancer were screened for moderate levels of fear of cancer recurrence (FCR). Forty-five were eligible (17 intervention and 28 control) and 34 completed 3-month follow-up (15 intervention and 21 control). Intervention   Mini-AFTERc, a single brief (30 min) structured telephone discussion with a specialist breast cancer nurse (SBCN) trained to target the antecedents of FCR. Outcomes   Feasibility and acceptability of Mini-AFTERc and the study design were assessed via recruitment, consent, retention rates, patient outcomes (measured at baseline, 2, 4, and 12 weeks), and post-study interviews with participants and SBCNs, which were guided by Normalisation Process Theory. Results   Mini-AFTERc was acceptable to patients and SBCNs. SBCNs believe the implementation of Mini-AFTERc to be feasible and an extension of discussions that already happen routinely. SBCNs believe delivery, however, at the scale required would be challenging given current competing demands for their time. Recruitment was impacted by variability in the follow-up practices of cancer centres and COVID-19 lockdown. Consent and follow-up procedures worked well, and retention rates were high. Conclusions   The study provided invaluable information about the potential challenges and solutions for testing the Mini-AFTERc intervention more widely where limiting high FCR levels is an important goal following recovery from primary breast cancer treatment.
dc.format.extent16
dc.format.extent1426306
dc.language.isoeng
dc.relation.ispartofPilot and Feasibility Studiesen
dc.subjectE-NDASen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.titleMini-AFTERc: a controlled pilot trial of a nurse-led psychological intervention for fear of breast cancer recurrenceen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Sir James Mackenzie Institute for Early Diagnosisen
dc.contributor.institutionUniversity of St Andrews. Centre for Interdisciplinary Research in Computational Algebraen
dc.contributor.institutionUniversity of St Andrews. School of Computer Scienceen
dc.identifier.doi10.1186/s40814-023-01431-x
dc.description.statusPeer revieweden


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