Please use this identifier to cite or link to this item: http://hdl.handle.net/11054/1765
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dc.contributorParikh, D.en_US
dc.contributorDiaz, A.en_US
dc.contributorBernardes, C.en_US
dc.contributorDe leso, P.en_US
dc.contributorThachil, Thanujaen_US
dc.contributorKar, G.en_US
dc.contributorStevens, M.en_US
dc.contributorGarvey, G.en_US
dc.date.accessioned2021-10-04T00:10:49Z-
dc.date.available2021-10-04T00:10:49Z-
dc.date.issued2021-
dc.identifier.govdoc01719en_US
dc.identifier.urihttp://hdl.handle.net/11054/1765-
dc.description.abstractAbstract Introduction Cancer patients in Australia’s Northern Territory (NT) face unique challenges to accessing cancer-related community and allied health services (referred here as ‘health services’). This is in part due to the NT’s unique geographic, socioeconomic and demographic profile. This paper describes the use of health services by cancer patients in the NT. Methods Adult cancer patients attending appointments at a cancer centre in Darwin, NT and who were diagnosed within the past five years were invited to participate in face-to-face interviews about their use of allied and community health services. A descriptive analysis of health services utilization was conducted. Results Of the 76 participants interviewed, 63% identified as non-Indigenous, 53% female and 45% lived in very remote areas. Mean age at interview was 58.7 years (SD 13.2). Overall, 82% of participants utilized at least one health service since their cancer diagnosis. All Indigenous participants used at least one service, while 28% of non-Indigenous participants did not use any health service. The services most frequently used by participants were community services (42%) and information sources (40%). Conclusion The findings from this study suggest there is variation in the type of community and allied health services used by NT cancer patients across clinical and demographic groups (including Indigenous status). Further qualitative enquiry is needed to better understand this variation, which may reflect differences in service preference, accessibility, health literacy of patients or patient engagement. Such knowledge may inform service delivery improvements to better support cancer patients through their cancer care pathway.en_US
dc.description.provenanceSubmitted by Gemma Siemensma (gemmas@bhs.org.au) on 2021-08-06T04:07:15Z No. of bitstreams: 0en
dc.description.provenanceApproved for entry into archive by Gemma Siemensma (gemmas@bhs.org.au) on 2021-10-04T00:10:48Z (GMT) No. of bitstreams: 0en
dc.description.provenanceMade available in DSpace on 2021-10-04T00:10:49Z (GMT). No. of bitstreams: 0 Previous issue date: 2021en
dc.titleThe utilization of allied and community health services by cancer patients living in regional and remote geographical areas in Australia.en_US
dc.typeJournal Articleen_US
dc.type.specifiedArticleen_US
dc.bibliographicCitation.titleSupportive Care in Canceren_US
dc.bibliographicCitation.volume29en_US
dc.bibliographicCitation.issue6en_US
dc.bibliographicCitation.stpage3209en_US
dc.bibliographicCitation.endpage3217en_US
dc.subject.healththesaurusHEALTH SERVICE USEen_US
dc.subject.healththesaurusCANCERen_US
dc.subject.healththesaurusREMOTEen_US
dc.subject.healththesaurusINDIGENOUSen_US
dc.subject.healththesaurusAUSTRALIAen_US
dc.identifier.doihttps://doi.org/10.1007/s00520-020-05839-6en_US
Appears in Collections:Research Output

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