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- 3Qualitative research
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Understanding the Provision of Palliative Care in the Context of Primary Health Care: Qualitative research findings from a pilot study in a community setting in Chile.
Download2009
Santos Salas, A., Cameron, B. L.
This pilot study looked at the provision of palliative care in the context of primary health care in a developing setting in Chile. RESEARCH OBJECTIVES: The study aimed to delineate the experience of palliative care from the perspective of patients and health care professionals; to examine...
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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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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...
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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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Family members providing home-based palliative care to older adults: The enactment of multiple roles
Download2008
Clemmer, S., Ward-Griffin, C., Forbes, D.
Canadians are experiencing increased life expectancy and chronic illness requiring end-of-life care. There is limited research on the multiple roles for family members providing home-based palliative care. Based on a larger ethnographic study of client-family-provider relationships in home-based...
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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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Developing a living with hope program for caregivers of family members with advanced cancer.
Download2007
Duggleby, Wendy, Holtslander, Lorraine, Williams, Allison, Degner, Lesley, Cammer, Allison, Wright, Karen
A theory-based intervention, the Living with Hope Program (LWHP), was designed to foster hope in caregivers of family members with advanced cancer. The LWHP was developed from qualitative data and using Harding and Higginson's recommendations for family caregiver interventions as a guide. The...
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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...