This decommissioned ERA site remains active temporarily to support our final migration steps to https://ualberta.scholaris.ca, ERA's new home. All new collections and items, including Spring 2025 theses, are at that site. For assistance, please contact erahelp@ualberta.ca.
Search
Skip to Search Results-
2012
St-Amant, O., DeForge, R.T., Ward-Griffin, C., McWilliam, C., Klosek, M., Forbes, D., Hall, J., Oudshoorn, A.
The hours of unpaid elder care by family members are projected to triple by 2038. Because living with dementia can inhibit decision-making abilities, family members are often besought to assist in this process. In this ethnographic study, relationships within home-based dementia care were...
-
2005
Kirk, A., Stewart, N., Biem, J., Morgan, D. G., D’Arcy, C., Crossley, M., Forbes, D.
The Canadian Institutes of Health Research (CIHR) New Emerging Team (NET) program was designed to provide 5 years of support for the creation of new teams or the development of existing teams of investigators conducting collaborative multidisciplinary research in identified areas of focus. A NET...
-
Knowledge exchange throughout the dementia care journey by Canadian rural community-based health care practitioners, persons with dementia, and their care partners: An interpretive descriptive study.
Download2012
Forbes, D. A., Thiessen, E., Blake, C. M., Morgan, D. G., Markle-Reid, M., Gibson, M., Finkelstein, S.
INTRODUCTION: Accessing, assessing, exchanging, and applying dementia care information can be challenging in rural communities for healthcare practitioners (HCPs), persons with dementia (PWD), and their care partners. The overall purpose of this research was to enable HCPs, care partners, and PWD...
-
The lived experience of family caregivers who provided end-of-life care to persons with advanced dementia.
Download2013
Peacock, S., Duggleby, W., Koop, P.
Objective: Dementia is a terminal illness, and family caregivers play a vital role in providing end-of-life care to their relative. The present study begins to address the paucity of research regarding end-of-life caregiving experience with dementia. Method: This study utilized Munhall's...
-
Gender differences in use and availability of home and community-based services for people with dementia.
Download2008
Henderson, S., Peacock, S., Kingston, D., Morgan, D., Leipert, B., Hawranik, P.
The purpose was to examine the use and availability of home and community-based services by men and women with dementia using data from the 2003 Canadian Community Health Survey. Variables of interest were based on the Andersen and Newman model and included predisposing, enabling, need, and use...
-
2014
In this paper we use Alvesson and Sandberg’s strategy of problematisation to analyse the assumptions embedded in the development and use of the concept of ‘care-giver burden’.We do this in order to develop an explanation as to why decades of research into the experience of providing home-based...
-
2013-01-01
Walls-Ingram, Sheena, O'Connell, Megan E., Cammer, Allison, Dal Bello-Haas, Vanina, Stewart, Norma, Crossley, Margaret, Innes, Anthea, Forbes, Dorothy, Morgan, Debra, Kirk, Andrew
Abstract Although only 20-50% of individuals with dementia are diagnosed, early diagnosis enables patients and families to access interventions and services, and plan for the future. The current study explored the experiences of rural family caregivers in the period leading up to a diagnostic...