Predicting family caregiver psychosocial functioning in palliative care
dc.contributor.author | Hudson, P. | |
dc.contributor.author | Hayman-White, K. | |
dc.contributor.author | Aranda, S. | |
dc.contributor.author | Kristjanson, Linda | |
dc.date.accessioned | 2017-01-30T14:47:12Z | |
dc.date.available | 2017-01-30T14:47:12Z | |
dc.date.created | 2008-11-12T23:32:27Z | |
dc.date.issued | 2006 | |
dc.identifier.citation | Hudson, Peter L and Hayman-White, Karla and Aranda, Sanchia and Kristjanson, Linda J. 2006. Predicting family caregiver psychosocial functioning in palliative care. Journal of Palliative Care 22 (3): 133-140. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/40959 | |
dc.description.abstract |
Health professionals are expected to support family caregivers of patients requiring palliative care. However, there is a dearth of empirical evidence to help clinicians identify caregivers who might be at risk of poor psychosocial functioning.This secondary analysis of baseline data from a larger study sought to determine if it was possible to predict the pyschosocial functioning of family caregivers who were supporting a relative with advanced incurable cancer.Data from 35 primary family caregivers obtained at the start of home-based palliative care services and five weeks later was used in the analysis. Instruments to measure careigver preparedness, competence, mastery, social support, anxiety, and self-efficacy were used.Cluster and logistic analyses revealed that self-reported 'anxiety' and competence' subscale total scores at time of commencement of home-based palliative care services were associated with caregivers at risk of lower levels of psychosocial functioning five weeks later.This study suggests that it may be possible to identify family caregivers who are at risk for poorer psychosocial functioning. However, replication in a larger sample is required before this screening approach can be recommended for clinical use. | |
dc.publisher | Centre for Bioethics, Clinical Research Institute of Montreal | |
dc.subject | support | |
dc.subject | anxiety | |
dc.subject | psychosocial functioning | |
dc.subject | social support | |
dc.subject | palliative care | |
dc.subject | Caregiver | |
dc.title | Predicting family caregiver psychosocial functioning in palliative care | |
dc.type | Journal Article | |
dcterms.source.volume | 22 | |
dcterms.source.number | 3 | |
dcterms.source.startPage | 133 | |
dcterms.source.endPage | 140 | |
dcterms.source.title | Journal of Palliative Care | |
curtin.identifier | EPR-1615 | |
curtin.accessStatus | Open access | |
curtin.faculty | Division of Health Sciences |