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Healthcare Providers’ Knowledge of Disordered Sleep, Sleep Assessment Tools, and Nonpharmacological Sleep Interventions for Persons Living with Dementia: A National Survey.
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Jones, A., Crick, K., Wielandt, P., Brown, C. A., Wilson, D.
Alarge proportion of personswith dementiawill also experience disordered sleep. Disordered sleep in dementia is a common reason for institutionalization and affects cognition, fall risk, agitation, self-care ability, and overall health and quality of life.This report presents findings of a survey...
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The lived experience of family caregivers who provided end-of-life care to persons with advanced dementia.
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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...
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The provision of end-of-life care by medical-surgical nurses working in acute care: A literature review.
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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...
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2013
Wilson, D., Magnus, R., Hewitt, J., Barnes, N., Vihos, J., Peterson, K.
This mixed-methods study addressed the problem that although waiting placement is considered a major hospital utilization issue, minimal evidence exists to highlight the extent of it and the personal impact of waiting placement. An analysis of two years of complete hospital data for the Canadian...
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2013
Low, G., Wilson, D., Wong, E., Ross, C., Stickland, M.
Among pulmonary rehabilitation attendees, we explored their tendency to downplay versus acknowledge physical and psychosocial health limitations, and the subsequent impact either strategy had on how they perceive their own aging process. Participants (N = 87) were 44 to 82 years of age, and...
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Hope against hope: Exploring the hopes and challenges of rural female caregivers of persons with advanced cancer.
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Thomas, R., Hallstrom, L., Williams, A., Cooper, R., Holtslander, L., Eby, J., Duggleby, W.
Background This paper focuses on the qualitative component of a study evaluating a hope intervention, entitled Living with Hope Program (LWHP), designed to foster hope in female caregivers of family members living with advanced cancer. The purpose of this research is to share, in the form of a...
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Hope and connection: The experience of family caregivers of persons with dementia living in a long term care facility.
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Duggleby, W., Schroeder, D., Nekolaichuk, C.
Background: Hope is a psychosocial resource that is essential for the psychological, spiritual, and physical well-being of family members caring for persons with dementia. A significant positive relationship has been found between hope and well-being in family caregivers of persons with dementia...
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Evaluation of the living with hope program for rural women caregivers of persons with advanced cancer.
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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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Development of a “Changes Toolkit” for Rural Older Palliative Patients and Their Family Caregivers
Download2012
Goodridge, Donna, Duggleby, W., Cooper, Lori J., Williams, A., Taniguichi, A., Leipert, B., Wilson, D., Marshall,D.
A “Changes Toolkit” was developed to help rural older palliative care patients and their caregivers deal with multiple concurrent transitions that cause disruption in their lives. The purpose of this article is to describe the development of the “Changes Toolkit” to support rural palliative...
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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...