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2014

Purkis, M. E., Ceci, C.

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...

2015-11-25

Forbes, D., Innes, A., Morgan, D. G., Quail, J. M., O'Connell, M. E., Teare, G. F., Kosteniuk, J. G., Stewart, N. J., Bello-Haas, V. D., Crossley, M., Kirk, A., Mou, H., McBain, L.

Background: Original studies published over the last decade regarding time trends in dementia report mixed results. The aims of the present study were to use linked administrative health data for the province of Saskatchewan for the period 2005/2006 to 2012/2013 to: (1) examine simultaneous...

2008

Forbes, D., Hogan, D., Gibson, M.

2008

Gibson, M., Forbes, D., Conn, D.

2013

Kang, S., Squires, J., Estabrooks, C. A., Cummings, G. G., Scott, S., Stevens, B., Hayduk, L.

Background Organizational context is recognized as an important influence on the successful implementation of research by healthcare professionals. However, there is relatively little empirical evidence to support this widely held view. Methods The objective of this study was to identify...

2014

Forbes, Dorothy A., Hammond-Collins, Karon, Peacock, Shelley

Background: With increasing rates of dementia among older adults, many people will be affected by this disease; either by having the disease or by caring for a relative with dementia. Due to a shift toward home and community-based care there will be an increase in the number of family caregivers...

2013

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...

2013

Duggleby, W., Gagnon, J.

Objective: Caring for terminally ill patients is complex, stressful, and at times distressing for nurses. Acute care hospitals continue to be the predominant place of death for terminally ill patients in most Western countries. The objective of the present literature review was to explore and...

2010

Johnson, C., Teare, G., Milke, D., Hutchinson, A.M., Maisey, S., Squires, J.E., Estabrooks, C.A.

Background: The Resident Assessment Instrument-Minimum Data Set (RAI-MDS) 2.0 is designed to collect the minimum amount of data to guide care planning and monitoring for residents in long-term care settings. These data have been used to compute indicators of care quality. Use of the quality...