Hostname: page-component-cd9895bd7-gbm5v Total loading time: 0 Render date: 2024-12-26T17:12:37.707Z Has data issue: false hasContentIssue false

Dementia Care Knowledge Sharing within a First Nations Community*

Published online by Cambridge University Press:  11 October 2013

Dorothy Forbes*
Affiliation:
Edmonton Clinic Health Academy, University of Alberta
Catherine Blake
Affiliation:
Arthur Labatt Family School of Nursing, University of Western Ontario
Emily Thiessen
Affiliation:
Edmonton Clinic Health Academy, University of Alberta
Sara Finkelstein
Affiliation:
Faculty of Medicine, University of Calgary
Maggie Gibson
Affiliation:
Veterans Care Program, Parkwood Hospital, St. Joseph’s Health Care
Debra G. Morgan
Affiliation:
Canadian Centre for Health and Safety in Agriculture, Department of Medicine, University of Saskatchewan
Maureen Markle-Reid
Affiliation:
School of Nursing, McMaster University
Ivan Culum
Affiliation:
Health and Rehabilitation Sciences, University of Western Ontario
*
Correspondence and requests for offprints should be sent to / La correspondance et les demandes de tirés-à-part doivent être addressees: Dorothy Forbes, Ph.D. Faculty of Nursing, Level 3 Edmonton Clinic Health Academy 11405 87 Avenue University of Alberta Edmonton, AB T6G 1C9 (dorothy.forbes@ualberta.ca)

Abstract

This article discusses the First Nations sample of a larger study on dementia care decisions and knowledge sharing. The purpose is to enhance understanding of the process of knowledge sharing among health care practitioners (HCPs), care partners, and persons with dementia (PWDs) within a rural First Nations community. A constructivist grounded theory methodology was used. Nineteen interviews were conducted at three points in time with two dementia care networks that included two PWDs, three care partners, and two HCPs. A sharing dementia care knowledge model was conceived, with the PWDs and their care partners at the centre. Knowledge sharing in the model was represented by three broad themes: (1) developing trusting relationships, (2) accessing and adapting the information, and (3) applying the information. Culturally sensitive approaches were essential to developing trusting relationships. Once developed, knowledge sharing through accessing, adapting, and applying the information was possible.

Résumé

Cet article discute l’échantillon d’une étude des Premières Nations plus vaste sur les décisions de soins de la démence et le partage des connaissances. L’objectif de cette étude est de mieux comprendre le processus de partage des connaissances entre les praticiens de la santé (PS), les partenaires de soins, et les personnes atteintes de démence (PAD) au sein d’une communauté rurale des Premières Nations. Une méthodologie de la théorie constructiviste ancrée a été utilisée. Dix-neuf entrevues ont ete menées à trois reprises avec deux réseaux de soins de la démence qui comprenait deux PAD, trois partenaires de soins, et deux PS. Un modèle, “Partage des connaissances sur les soins de la démence,” a été conçue, centrée sur les PAD et leurs partenaires de soins. Trois grands thèmes du partage des connaissances sont representées dans le modèle: (1) le développement des relations de confiance, (2) l’accès et l’adaptation aux informations, et (3) application des informations. Des approches sensibles à la culture sont essentiels pour le développement des relations de confiance. Une fois que les relations ont été développées, le partage des connaissances grâce à l’accès, l’adaptation et l’application des informations est devenu possible.

Type
Articles
Copyright
Copyright © Canadian Association on Gerontology 2013 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

*

Funding for this study – Developing Quality Dementia Care Decisions through Knowledge Exchange in Rural Settings – was gratefully received from the Alzheimer Society of Canada, in partnership with the Canadian Nurses Foundation and the Canadian Institutes of Health Research – Institute of Aging.

References

Aboriginal Affairs and Northern Development Canada. (2012). Key milestones. Retrieved on September 6, 2013, fromwww.aandc-aadna.gc.ca.Google Scholar
Alzheimer Disease International & World Health Organization. (2012). Dementia a public health priority. Geneva, Switzerland: World Health Organization.Google Scholar
Alzheimer Society of Canada. (2008). Progression of Alzheimer’s disease: An overview. Retrieved on October 4, 2012 fromhttp://www.alzheimer.ca/en/We-can-help/Resources/∼/media/Files/national/Progression-series/progression_overview_2008_e.ashx.Google Scholar
Alzheimer Society of Canada. (2010). The rising tide: The impact of dementia on Canadian society: Executive summary. Toronto, ON: Alzheimer Society of Canada.Google Scholar
Alzheimer Society of Ontario. (2013) First Link overview. Retrieved on September 6, 2013 fromhttp://www.akeresourcecentre.org/files/FirstLink/Overview.pdf.Google Scholar
Andrews, M. E., Morgan, D. G., & Stewart, N. J. (2010). Dementia awareness in northern nursing practice. Canadian Journal of Nursing Research, 42(1), 5673.Google Scholar
Bartlett, R., & O’Connor, D. (2010). Broadening the dementia debate: Towards social citizenship. Bristol, UK: Policy Press.Google Scholar
Charmaz, K. (2009). Constructing grounded theory: A practical guide through qualitative analysis. Thousand Oaks, CA: Sage.Google Scholar
Cook, A. (2008). Dementia and well-being: Possibilities and challenges. Edinburgh, Scotland: Dunedin Academic Press.Google Scholar
Craft, S. (2009). The role of metabolic disorders in Alzheimer’s disease and vascular dementia: Two roads converged. Archives of Neurology, 66(3), 300305.CrossRefGoogle ScholarPubMed
Department of Health. (2012). Prime Minister’s challenge on dementia: Delivering major improvements in dementia care and research by 2015. London, UK: Author.Google Scholar
Donath, C., Gräßel, E., Großfeld-Schmitz, M., Menn, P., Lauterberg, J., Wunder, S., et al. (2010). Effects of general practitioner training and family support services on the care of home-dwelling dementia patients: Results of a controlled cluster-randomized study. BMC Health Services Research, 10(314), 114. doi: 10.1186/1472-6963-10-314CrossRefGoogle ScholarPubMed
Estey, E., Kmetic, A., & Reading, J. (2010). Thinking about aboriginal KT: Learning from the Network Environments for Aboriginal Health Research British Columbia (NEARBC). Canadian Journal of Public Health, 101(1), 8386.Google Scholar
Estey, E., Smylie, J., & Macaulay, A. (2009). Aboriginal knowledge translation: Understanding and respecting the distinct needs of Aboriginal communities in research. Commissioned by the CIHR-Institute of Aboriginal Peoples’ Health.Google Scholar
Finkelstein, S., Forbes, D., & Richmond, C. (2012). Formal dementia care among first nations in southwestern Ontario. Canadian Journal on Aging, 31(3), 257270.CrossRefGoogle ScholarPubMed
First Nations Centre. (2005). First Nations Regional Longitudinal Health Survey (RHS) 2002/2003: Results for adults, youth and children living in First Nations communities. Ottawa, ON: First Nations Centre, National Aboriginal Health Organization.Google Scholar
Fisk, J., Beattie, B. L., & Donnelly, M. (2007). Ethical considerations for decision making for treatment and research participation. Alzheimer’s & Dementia, 3(4), 411417.CrossRefGoogle ScholarPubMed
Forbes, D. A., Finkelstein, S., Blake, C., Gibson, M., Morgan, D. G., Markle-Reid, M., et al. (2012). 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. Journal of Rural and Remote Health, 12(4), 2201.Google Scholar
Forbes, D. A., Markle-Reid, M., Hawranik, P., Peacock, S., Kingston, D., Morgan, D., et al. (2008). Availability and acceptability of Canadian home and community-based services: Perspectives of family caregivers of persons with dementia. Home Health Care Services Quarterly, 27(2), 7599.Google Scholar
Henderson, J. N., & Henderson, L. C. (2002). Cultural construction of disease: A “supernormal” construct of dementia in an American Indian tribe. Journal of Cross-Cultural Gerontology, 17, 197212.CrossRefGoogle Scholar
Hendrie, H. C., Hall, K. S., Pillay, N., Rodgers, D., Prince, C., Norton, J., et al. (1993). Alzheimer’s disease is rare in Cree. International Psychogeriatrics, 5(1), 514.Google Scholar
Indian and Northern Affairs Canada. (2008). Aboriginal demography: Population, household and family projections, 2001–2026. Ottawa, ON: Indian and Northern Affairs Canada/Canada Mortgage and Housing Corporation (CMHC).Google Scholar
Keady, J. (2010). Guest editorial. Journal of Mental Health Training, Education, and Practice, 5(3), 23.CrossRefGoogle Scholar
Keady, J., Campbell, S., Barnes, H., Ward, R., Li, X., Swarbrick, C., et al. (2012). Neighbourhoods and dementia in the health and social care context: A realist review of the literature and implications for UK policy development. Reviews in Clinical Gerontology, 22(2), 150163. doi: 10.1017/S0959259811000268CrossRefGoogle Scholar
Lincoln, Y. S., & Guba, E. G. (1985). Naturalistic Inquiry. Newbury Park, CA: Sage.CrossRefGoogle Scholar
McAiney, C., Harvey, D., & Schulz, M. E. (2008). First Link: Strengthening primary care partnerships for dementia support. Canadian Journal of Community Mental Health, 27(2), 117127.CrossRefGoogle Scholar
McCormack, B. (2002). The person of the voice: Narrative identities in informed consent. Nursing Philosophy, 3(2) 114119.CrossRefGoogle Scholar
O’Connor, D. (2010). Personhood and dementia: Toward a relational framework for assessing decisional capacity. Journal of Mental Health Training, Education, and Practice, 5(3), 2230.Google Scholar
O’Connor, D., & Purves, B. (Eds). (2009). Decision-making, personhood and dementia: Exploring the interface. London, UK: Jessica Kingsley.Google Scholar
Patterson, C., Feightner, J. W., Garcia, A., Hsiung, G. Y., MacKnight, C., & Sadovnick, A. D. (2008). Diagnosis and treatment of dementia: 1. Risk assessment and primary prevention of Alzheimer disease. Canadian Medical Association Journal, 178(5), 548556.CrossRefGoogle ScholarPubMed
Prince, M., Bryce, R., & Ferri, C. (2011). World Alzheimer Report 2011: The benefits of early diagnosis and intervention: Executive summary. London, UK: Alzheimer’s Disease International.Google Scholar
Schreiber, R. S. (2001). The “how to” of grounded theory: Avoiding the pitfalls. In Schreiber, R. S. & Stern, P. N. (Eds.), Using grounded theory in nursing (pp. 5583). New York, NY: Springer.Google Scholar
Statistics Canada. (2012). 2011 Census. Retrieved on December 12, 2012, fromhttp://www5.statcan.gc.ca.Google Scholar
Waldram, J. B. (2008). Aboriginal healing in Canada: Studies in therapeutic meaning and practice. Aboriginal Healing Foundation Research Series. Retrieved on September 6, 2013, fromhttp://www.ahf.ca/downloads/aboriginal-healing-in-Canada.pdf.Google Scholar
Weiner, M. F., Rosenberg, R. N., Svetlik, D., Hynan, L. S., Womack, K. B., White, C. 3rd, et al. (2003). Comparison of Alzheimer’s disease in Native Americans and Whites. International Psychogeriatrics, 15(4), 367375.CrossRefGoogle ScholarPubMed