Search
Skip to Search Results- 13Palliative care
- 3Qualitative research
- 2Caregivers
- 2Developing countries
- 2Family caregivers
- 2Knowledge exchange
-
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...
-
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...
-
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...
-
Creating Neighbourhood Groupings Based on Built Environment Features to Facilitate Health Promotion Activities
Download2012
VanSpronsen, Eric, Plotnikoff, Ronald C., Vallianatos, Helen, Schopflocher, Donald, Raine, Kim D., Spence, John C., Nykiforuk, Candace I.J.
OBJECTIVES: Detailed assessments of the built environment often resist data reduction and summarization. This project sought to develop a method of reducing built environment data to an extent that they can be effectively communicated to researchers and community stakeholders. We aim to help in...
-
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...
-
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...
-
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...
-
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?...