References
- Afram, B., Verbeek, H., Bleijlevens, M. H. C., & Hamers, J. P. H. (2015). Needs of informal caregivers during transition from home towards institutional care in dementia: A systematic review of qualitative studies. International Psychogeriatrics, 27(6), 891–902.
- Alzheimer Society of Canada. (2017). Dementia numbers in Canada. Retrieved from www.alzheimer.ca
- Adams, K. B. (2006). The transition to caregiving: The experience of family members embarking on the dementia caregiving career. Journal of Gerontological Social Work, 47(3-4), 3–29.
- Braun, V., & Clarke, V. (2006). Using thematic analysis in psychology. Qualitative Research in Psychology, 3, 77–101.
- Donelan, K., Falik, M., & Deroches, C. M. (2001). The costs of caring: Impact of dementia on family caregivers. Women’s Health Issues, 11, 185–200.
- Ducharme, F., Levesque, L., Lachance, L., Giroux, F., Legault, A., & Preville, M. (2005). ‘Taking care of myself’: Efficacy of an intervention programme for caregivers of a relative with dementia living in a long-term care setting. Dementia, 4(1), 23–47.
- Duggleby, W. (2005). What about focus group interaction data? Qualitative Health Research, 15(6), 832–840.
- Duggleby, W., Swindle, J., Peacock, S., & Ghosh, S. (2011). A mixed methods study of hope, transitions, and quality of life in family caregivers of persons with Alzheimer’s disease. BMC Geriatrics, 11(88) 1–12. Retrieved from http://www.biomedcentral.com/1471-2318/11/88. doi: 10.1186/1471-2318-11-88
- Duggleby, W., Schroeder, D., & Nekolaichuk, C. (2013). Hope and connection: The experience of family caregivers of persons with dementia living in a long-term care facility. BMC Geriatrics, 13, 112.
- Fast, J., Eales, J., & Keating, N. (2001). Economic impact of health, income security and labour policies on informal caregivers of frail seniors. Ottawa, Ontario: Research Directorate. Status of Women Canada.
- Garity, J. (2006). Caring for a family member with Alzheimer’s disease: Coping with caregiver burden post nursing home placement. Journal of Gerontological Nursing, 32(6), 39–48.
- Gaugler, J. E., Mittleman, M. S., Hepburn, K., & Newcomer, R. (2012). Identifying at-risk dementia caregivers following institutionalisation. The nursing home admission-burden and nursing home admission-depression prognostic tools. Journal of Applied Gerontology, 33(5), 624–646.
- Gilliland, M. P., & Bush, H. A. (2001). Social support for family caregivers: Toward a situation-specific theory. Journal of Theory Construction and Testing, 5(2), 53–62.
- Graneheim, U. H., Johansson, A., & Lindgren, M. (2014). Family caregivers’ experiences of relinquishing the care of a person with dementia to a nursing home: Insights from a meta-ethnographic study. Scandinavian Journal of Caring Science, 28, 215–224.
- Gruenfeld, E., Coyle, D., Whelan, T., Clinch, J., Reyno, L., Earle, C., & Glossop, R. (2004). Family caregiver burden: Results of a longitudinal study of breast cancer patients and their principal caregivers. Canadian Medical Association Journal, 170, 1795–1801.
- Hogsnes, L., Melin-Johansson, C., Norbergh, K. G., & Danielson, E. (2014). The existential life situations of spouses of persons with dementia before and after relocating to a Nursing home. Aging & Mental Health, 18(2), 152–160.
- Johannson, A., Graneheim, U. H., Ruzin, H. O., & Lindgren, B. M. (2014). Remaining connected despite separation—former family caregivers’ experiences of aspects that facilitate and hinder the process of relinquishing the care of a person with dementia to a nursing home. Aging & Mental Health, 18(8), 1029–1036.
- Kellett, U. M. (1999). Transition in care: Family carers’ experience of nursing home placement. Journal of Advanced Nursing, 2(6), 1474–1481.
- Koplow, S. M., Gallo, A. M., Knafl, K. A., Vincent, C., Paun, O., & Gruss, V., (2015). Family caregivers define and manage the nursing home placement process. Journal of Family Nursing, 2 (3), 469–493.
- Lieberman, M. A., & Fisher, L. (2001). The effects of nursing home placement on family caregivers of patients with Alzheimer’s disease. The Gerontologist, 41(6), 819–826.
- Meleis, A. I., & Trangenstein, P. A. (1994). Facilitating transitions: Redefinition of the nursing mission. Nursing Outlook, 42, 255–259.
- Moyle, W., Edwards, H., & Clinton, M. (2002). Living with loss: Dementia and the family caregiver. Australian Journal of Advanced Nursing, 19(3), 25–32.
- Onwuegbuzie, A. J., Dickinson, W. B., Leech, N. L., & Zoran, A. G. (2009). A qualitative framework for collecting and analyzing data in focus group research. International Journal of Qualitative Methods, 8(3), 1–22.
- Pote, S. C., & Wright, S. L. (2018). Evaluating anticipatory grief as a moderator of marital satisfaction for spousal caregivers of individuals with dementia. Educational Gerontology, 44(2-3), 196–207.
- Ryan, A. A., & Scullion, H. F. (2000). Nursing home placement: An exploration of the experiences of family carers. Journal of Advanced Nursing, 32(5), 1187–1195.
- Schultz, R., Belle, S. H., Czaja, S. J., McGinnis, K. A., Stevens, A., & Zhang, S. (2004). Long-term care placement of dementia patients and caregiver health and well-being. JAMA: Journal of the American Medical Association, 292(8), 961–967.
- Strang, V. R., Koop, P. M., Dupuis-Blanchard, S., Nordstrom, M., & Thompson, B. (2006). Family caregivers and transition to long-term care. Clinical Nursing Research, 15(1), 27–45.
- Tornatore, J. B., & Grant, L. A. (2002). Burden among family caregivers of persons with Alzheimer’s disease in nursing homes. The Gerontologist, 42(4), 497–506.
- Wubker, A., Zwakhalen, S. M. G., Challis, D., Suhonen, R., Karlsson, S., Zabalegui, A., … Sauderland, D. (2015). Costs of care for people with dementia just before and after nursing home placement: primary data from 8 European countries. European Journal of Health Economics, 16(7), 689–707.