These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
146 related articles for article (PubMed ID: 20795582)
1. Time travel: the lived experience of providing feeding assistance to a family member with dementia. Lopez RP; Amella EJ Res Gerontol Nurs; 2011 Apr; 4(2):127-34. PubMed ID: 20795582 [TBL] [Abstract][Full Text] [Related]
2. Institutionalized elders with dementia: collaboration between family caregivers and nursing home staff in Taiwan. Lau WY; Shyu YI; Lin LC; Yang PS J Clin Nurs; 2008 Feb; 17(4):482-90. PubMed ID: 18205680 [TBL] [Abstract][Full Text] [Related]
3. Mealtime experiences of families with dementia. Keller HH; Edward HG; Cook C Am J Alzheimers Dis Other Demen; 2006 Dec-2007 Jan; 21(6):431-8. PubMed ID: 17267376 [TBL] [Abstract][Full Text] [Related]
4. Home health aide services: barriers perceived by dementia family caregivers. Liken MA; King SK Home Healthc Nurse; 1995; 13(6):60-8. PubMed ID: 8698595 [TBL] [Abstract][Full Text] [Related]
5. [An analysis of the meaning of respite for family caregivers of elderly with dementia]. Song MR; Lee YM; Cheon SH J Korean Acad Nurs; 2010 Aug; 40(4):482-92. PubMed ID: 20820115 [TBL] [Abstract][Full Text] [Related]
6. Renewing everyday hope: the hope experience of family caregivers of persons with dementia. Duggleby W; Williams A; Wright K; Bollinger S Issues Ment Health Nurs; 2009 Aug; 30(8):514-21. PubMed ID: 19591026 [TBL] [Abstract][Full Text] [Related]
7. Living with loss: dementia and the family caregiver. Moyle W; Edwards H; Clinton M Aust J Adv Nurs; 2002; 19(3):25-31. PubMed ID: 12002626 [TBL] [Abstract][Full Text] [Related]
8. Knowing the diagnosis and counselling the relatives of a person with dementia: the perspective of home nurses and home care workers in Belgium. Roelands M; Van Oost P; Depoorter A; Verloo H Health Soc Care Community; 2005 Mar; 13(2):112-24. PubMed ID: 15717913 [TBL] [Abstract][Full Text] [Related]
9. Empowering older people with early dementia and family caregivers: a participatory action research study. Nomura M; Makimoto K; Kato M; Shiba T; Matsuura C; Shigenobu K; Ishikawa T; Matsumoto N; Ikeda M Int J Nurs Stud; 2009 Apr; 46(4):431-41. PubMed ID: 17983619 [TBL] [Abstract][Full Text] [Related]
10. Family caregivers and transition to long-term care. Strang VR; Koop PM; Dupuis-Blanchard S; Nordstrom M; Thompson B Clin Nurs Res; 2006 Feb; 15(1):27-45. PubMed ID: 16410621 [TBL] [Abstract][Full Text] [Related]
11. Seeking to understand telephone support for dementia caregivers. Salfi J; Ploeg J; Black ME West J Nurs Res; 2005 Oct; 27(6):701-21. PubMed ID: 16157943 [TBL] [Abstract][Full Text] [Related]
12. Family caregivers' subjective experiences of satisfaction in dementia care: aspects of burden, subjective health and sense of coherence. Andrén S; Elmståhl S Scand J Caring Sci; 2005 Jun; 19(2):157-68. PubMed ID: 15877641 [TBL] [Abstract][Full Text] [Related]
13. Caregiving transitions: changes in depression among family caregivers of relatives with dementia. Collins C; Stommel M; Wang S; Given CW Nurs Res; 1994; 43(4):220-5. PubMed ID: 8047426 [TBL] [Abstract][Full Text] [Related]
14. Psychosocial intervention for family caregivers of people with dementia reduces caregiver's burden: development and effect after 6 and 12 months. Signe A; Elmståhl S Scand J Caring Sci; 2008 Mar; 22(1):98-109. PubMed ID: 18269429 [TBL] [Abstract][Full Text] [Related]
15. Use of home care services effectively reduces feelings of burden among family caregivers of disabled elderly in Japan: preliminary results. Kumamoto K; Arai Y; Zarit SH Int J Geriatr Psychiatry; 2006 Feb; 21(2):163-70. PubMed ID: 16416464 [TBL] [Abstract][Full Text] [Related]
16. Relationships between income, subjective health and caregiver burden in caregivers of people with dementia in group living care: a cross-sectional community-based study. Andrén S; Elmståhl S Int J Nurs Stud; 2007 Mar; 44(3):435-46. PubMed ID: 17078957 [TBL] [Abstract][Full Text] [Related]
17. The experience of providing care in the early stages of dementia: an interpretative phenomenological analysis. Quinn C; Clare L; Pearce A; van Dijkhuizen M Aging Ment Health; 2008 Nov; 12(6):769-78. PubMed ID: 19023728 [TBL] [Abstract][Full Text] [Related]
18. [Family caregivers' expectations of respite care of patients with dementia]. Voutilainen P; Korpiniitty S Hoitotiede; 1997; 9(1):25-32. PubMed ID: 9407793 [TBL] [Abstract][Full Text] [Related]
19. Family members' experiences caring for patients with advanced head and neck cancer receiving tube feeding: a descriptive phenomenological study. Penner JL; McClement S; Lobchuk M; Daeninck P J Pain Symptom Manage; 2012 Oct; 44(4):563-71. PubMed ID: 22699088 [TBL] [Abstract][Full Text] [Related]
20. Adjusting to mealtime change within the context of dementia. Genoe MR; Keller HH; Martin LS; Dupuis SL; Reimer H; Cassolato C; Edward G Can J Aging; 2012 Jun; 31(2):173-94. PubMed ID: 22588331 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]