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Results: 1 to 20 of 112

Similar articles for PubMed (Select 21244457)

1.

Wellbeing among people with dementia and their next of kin over a period of 3 years.

Holst G, Edberg AK.

Scand J Caring Sci. 2011 Sep;25(3):549-57. doi: 10.1111/j.1471-6712.2010.00863.x. Epub 2011 Jan 19.

PMID:
21244457
2.
3.

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. doi: 10.1111/j.1471-6712.2007.00498.x.

PMID:
18269429
5.

The relationship between caregiver burden, caregivers' perceived health and their sense of coherence in caring for elders with dementia.

Andrén S, Elmståhl S.

J Clin Nurs. 2008 Mar;17(6):790-9. doi: 10.1111/j.1365-2702.2007.02066.x.

PMID:
18279282
6.

[Caregiver burden in dementia: evaluation with a Japanese version of the Zarit caregiver burden interview].

Hirono N, Kobayashi H, Mori E.

No To Shinkei. 1998 Jun;50(6):561-7. Japanese.

PMID:
9656252
7.
8.

Predictors of change and continuity in home care for dementia patients.

Vernooij-Dassen M, Felling A, Persoon J.

Int J Geriatr Psychiatry. 1997 Jun;12(6):671-7.

PMID:
9215952
9.

Stress in the caregivers of Alzheimer's patients: an experimental investigation in Italy.

Aguglia E, Onor ML, Trevisiol M, Negro C, Saina M, Maso E.

Am J Alzheimers Dis Other Demen. 2004 Jul-Aug;19(4):248-52.

PMID:
15359564
11.

Family caregiving in dementia--an analysis of the caregiver's burden and the "breaking-point" when home care becomes inadequate.

Annerstedt L, Elmståhl S, Ingvad B, Samuelsson SM.

Scand J Public Health. 2000 Mar;28(1):23-31.

PMID:
10817311
12.

Quality of life in spite of an unpredictable future: the next of kin of patients with multiple sclerosis.

Liedström E, Isaksson AK, Ahlström G.

J Neurosci Nurs. 2010 Dec;42(6):331-41.

PMID:
21207771
13.

Next of kin's experience of powerlessness and helplessness in palliative home care.

Milberg A, Strang P, Jakobsson M.

Support Care Cancer. 2004 Feb;12(2):120-8. Epub 2003 Dec 18.

PMID:
14685835
14.

Family caregiving in dementia: prediction of caregiver burden 12 months after relocation to group-living care.

Elmståhl S, Ingvad B, Annerstedt L.

Int Psychogeriatr. 1998 Jun;10(2):127-46.

PMID:
9677500
15.

Evaluation of advanced home care (AHC). The next-of-kin's experiences.

Rollison B, Carlsson M.

Eur J Oncol Nurs. 2002 Jun;6(2):100-6.

PMID:
12849600
16.

Patient and caregiver characteristics associated with depression in caregivers of patients with dementia.

Covinsky KE, Newcomer R, Fox P, Wood J, Sands L, Dane K, Yaffe K.

J Gen Intern Med. 2003 Dec;18(12):1006-14.

17.

[Caregiver burden in relatives of persons with schizophrenia: an overview of measure instruments].

Reine G, Lancon C, Simeoni MC, Duplan S, Auquier P.

Encephale. 2003 Mar-Apr;29(2):137-47. Review. French.

PMID:
14567165
18.

Caregiver burden among caregivers of Koreans with dementia.

Kim MD, Hong SC, Lee CI, Kim SY, Kang IO, Lee SY.

Gerontology. 2009;55(1):106-13. doi: 10.1159/000176300. Epub 2008 Nov 20.

PMID:
19023194
19.

Use of the Zarit scale for assessing caregiver burden and collapse in caregiving at home in dementias.

Gort AM, Mingot M, Gomez X, Soler T, Torres G, Sacristán O, Miguelsanz S, Nicolas F, Perez A, de Miguel M, Cabau J.

Int J Geriatr Psychiatry. 2007 Oct;22(10):957-62.

PMID:
17299807
20.

Gender of demented patients and specific family relationship of caregiver to patients influence mental fatigue and burdens on relatives as caregivers.

Nagatomo I, Akasaki Y, Uchida M, Tominaga M, Hashiguchi W, Takigawa M.

Int J Geriatr Psychiatry. 1999 Aug;14(8):618-25.

PMID:
10489652
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