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Design and introduction of a quality of life assessment and practice support system: perspectives from palliative care settings
Download2018-01-01
Sawatzky, Richard, Laforest, Esther, Schick-Makaroff, Kara, Stajduhar, Kelli, Reimer-Kirkham, Sheryl, Krawczyk, Marian, Öhlén, Joakim, McLeod, Barbara, Hilliard, Neil, Tayler, Carolyn, Cohen, S. Robin
Background: Quality of life (QOL) assessment instruments, including patient-reported outcome measures (PROMs) and patient-reported experience measures (PREMs), are increasingly promoted as a means of enabling clinicians to enhance person-centered care. However, integration of these instruments...
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2014
Keating, N., Wilson, D.M., Williams, B.E.C.
This report documents the findings of a mixed-methods study focused on the advanced directives of 182 residents of three LTC facilities in southern Ontario, Canada. Although almost all had a completed advance directive within 3 months of death, most did not have a palliative designation or...
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The preferred place of last days: Results of a representative population-based public survey.
Download2013
Houttekier, D., Deliens, L., Cohen, J., Hewitt, J. A., Wilson, D. M.
Background: The place of death is of considerable interest now, yet few studies have determined public preferences for place of end-of-life (EOL) care or final days of life. Objective: A survey was designed to answer three questions: (1) What are public preferences for the place of last days?...
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Evaluation of the living with hope program for rural women caregivers of persons with advanced cancer.
Download2013
Hampton, M., Cooper, D., Holstlander, L., Ghosh, S., Williams, A., Duggleby, W., McLean, R. T., Hallstrom, L.
Background Hope has been identified as a key psychosocial resource among family caregivers to manage and deal with the caregiver experience. The Living with Hope Program is a self-administered intervention that consists of watching an international award winning Living with Hope film and...
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2012
Duggleby, W., Williams, A., McIntosh, M.J., Eby, J., Leipert, B.
Most informal caregivers in Canada are women (Cranwick, 1997; Fast, Eales & Keating, 2001; Kaden & MacDonald, 1990; MacLean, Cairn, & Sellick, 1998). Women caring for dying persons at the end-of-life have been identified in the literature as those most likely to experience negative physical and...
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2012
Mayo, K., Fisher, J. W., Wilson, D. M., MacLeod, R. D., Newman, N., Thompson, R.
AIM: This project investigated New Zealanders' views about palliative care and local hospice services. METHOD: A representative population-based sample of 1011 New Zealanders completed an online survey. RESULTS: The age, gender, and geographic region of the 1011 participants were broadly...
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Participatory knowledge exchange to support palliative care in Chile: Lessons learned through global health research.
Download2011
deMoissac, D., Cameron, B. L., Santos Salas, A.
The authors designed a participatory qualitative research study to develop a collaborative partnership between palliative care practitioners in Canada and in Chile. The research goal was to support the provision of palliative care in vulnerable settings through a participatory knowledge exchange...