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dc.contributor.authorHudson, P
dc.contributor.authorTrauer, T
dc.contributor.authorKelly, B
dc.contributor.authorO'Connor, Moira
dc.contributor.authorThomas, K
dc.contributor.authorSummers, M
dc.contributor.authorZordan, R
dc.contributor.authorWhite, V
dc.date.accessioned2017-01-30T11:48:23Z
dc.date.available2017-01-30T11:48:23Z
dc.date.created2013-09-24T20:01:10Z
dc.date.issued2013
dc.identifier.citationHudson, Peter and Trauer, Tom and Kelly, Brian and O'Connor, Moira and Thomas, Kristina and Summers, Michael and Zordan, Rachel and White, Vicki. 2013. Reducing the psychological distress of family caregivers of home-based palliative care patients: Short-term effects from a randomised controlled trial. Psycho-Oncology. 22 (9): pp. 1987-1993.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/15171
dc.identifier.doi10.1002/pon.3242
dc.description.abstract

Background: Palliative care is expected to incorporate comprehensive support for family caregivers given that many caregivers suffer psychological morbidity. However, systematically implemented evidence-based psychological support initiatives are lacking. Aim: The objective of this study was to prepare caregivers for the role of supporting a patient with advanced cancer receiving home-based palliative care by offering a one-to-one psycho-educational intervention. We hypothesised that primary family caregivers who participated in the intervention would report decreased psychological distress (primary outcome), fewer unmet needs and increased levels of perceived preparedness, competence and positive emotions. Methods: A three-arm randomised controlled trial was conducted comparing two versions of the intervention (one face-to-face visit versus two visits) plus standard care to a control group (standard care) across four sites in Australia.Results: A total of 298 participants were recruited; 148 were in the Control condition, 57 in Intervention 1 (one visit) and 93 in Intervention 2 (two visits). Relative to participants in the control group; the psychological well-being of participants in the intervention condition was improved by a small amount but non-significantly. No significant reduction in unmet needs or improvements in positive aspects of caregiving amongst the intervention group were identified. However, the intervention demonstrated significant improvements in participants' levels of preparedness and competence for Intervention 2. Conclusion/implications: This research adds to accumulating body of evidence demonstrating that relatively short psycho-educational interventions can enable family caregivers to feel more prepared and competent in the role of supporting a dying relative. Further investigation is required to determine the longer term outcomes of such interventions.

dc.publisherWiley InterScience
dc.titleReducing the psychological distress of family caregivers of home-based palliative care patients: Short-term effects from a randomised controlled trial.
dc.typeJournal Article
dcterms.source.volume22
dcterms.source.number9
dcterms.source.startPage1987
dcterms.source.endPage1993
dcterms.source.issn1057-9249
dcterms.source.titlePsycho-Oncology
curtin.department
curtin.accessStatusFulltext not available


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