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dc.contributor.authorFry, A.
dc.contributor.authorCull, A.
dc.contributor.authorAppleton, Sally
dc.contributor.authorRush, Robert
dc.contributor.authorHolloway, Susan
dc.contributor.authorGorman, Dermot
dc.contributor.authorCetnarskyj, Roseanne
dc.contributor.authorThomas, R.
dc.contributor.authorCampbell, J.
dc.contributor.authorAnderson, E.
dc.contributor.authorSteel, M.
dc.contributor.authorPorteous, Mary
dc.contributor.authorCampbell, Harry
dc.date.accessioned2018-07-20T08:57:10Z
dc.date.available2018-07-20T08:57:10Z
dc.date.issued2003-08-12
dc.identifier.citationFry, A., Cull, A., Appleton, S., Rush, R., Holloway, S., Gorman, D., Cetnarskyj, R., Thomas, R., Campbell, J., Anderson, E., Steel, M., Porteous, M. & Campbell, H. (2003) A randomised controlled trial of breast cancer genetics services in South East Scotland: psychological impact, British Journal of Cancer, vol. 89, , pp. 653-659,
dc.identifier.issn70920
dc.identifier.urihttps://eresearch.qmu.ac.uk/handle/20.500.12289/459
dc.identifier.urihttp://dx.doi.org/10.1038/sj.bjc.6601170
dc.description.abstractThis study compared the psychological impact of two models of breast cancer genetics services in South East Scotland. One hundred and seventy general practices were randomised to refer patients to the existing standard regional service or the novel community based service. Participants completed postal questionnaires at baseline (n¼373), 4 weeks (n¼276) and 6 months (n¼263) to assess perceived risk of breast cancer, subjective and objective understanding of genetics and screening issues, general psychological distress, cancer worry and health behaviours. For participants in both arms of the trial, there were improvements in subjective and objective understanding up to 4 weeks which were generally sustained up to 6 months. However, improvements in subjective understanding for the women at low risk of breast cancer (i.e. not at significantly increased risk) in the standard service arm did not reach statistical significance. Cancer worry was significantly reduced at 6 months for participants in both arms of the trial. The two models of cancer genetics services tested were generally comparable in terms of the participants’ psychological outcomes. Therefore, decisions regarding the implementation of the novel community-based service should be based on the resources required and client satisfaction with the service
dc.format.extent653-659
dc.relation.ispartofBritish Journal of Cancer
dc.titleA randomised controlled trial of breast cancer genetics services in South East Scotland: psychological impact
dc.typearticle
dcterms.accessRightsrestricted
dc.description.facultyNO DIVISION
dc.description.volume89
dc.identifier.doidoi:10.1038/sj.bjc.6601170
dc.description.ispublishedpub
dc.description.eprintid459
rioxxterms.typearticle
rioxxterms.publicationdate12/08/2003
qmu.authorRush, Robert
dc.description.statuspub
dc.description.number4


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