|
Sign In to gain access to subscriptions and/or personal tools.
|
Informal Care for the Disabled Elderly
A Critique of Recent Literature
Emily K. Abel
University of California, Los Angeles
Most studies of informal care for the disabled elderly are based on structured interviews, which are analyzed statistically, and they focus on two issues that lend themselves to quantification - the tasks caregivers perform and the stress they experience. The focus on chores restricts researchers' understanding of the experience of caregivers. Task-oriented research may be particularly inappropriate for an activity dominated by women. Because stress has critical implications for public health, researchers have attempted to identify caregivers most at risk of stress and to evaluate interventions. Although these studies have provided useful information for practitioners, the preoccupation with stress compels researchers to miss essential aspects of the caregiving experience and restricts the range of policy recommendations. Researchers should employ qualitative, as well as quantitative, methodologies and should incorporate the theoretical insights of a wide range of disciplines. Because scholars in the field of women's studies have directed considerable attention to personal relationships and caregiving issues, their writings may be especially useful for charting an agenda for research.
Research on Aging, Vol. 12, No. 2,
139-157 (1990)
DOI: 10.1177/0164027590122001

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
P. Bracke, W. Christiaens, and N. Wauterickx
The Pivotal Role of Women in Informal Care
Journal of Family Issues,
October 1, 2008;
29(10):
1348 - 1378.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Perry
Daughters Giving Care to Mothers Who Have Dementia: Mastering the 3 R's of (Re)Calling, (Re)Learning, and (Re)Adjusting
Journal of Family Nursing,
February 1, 2004;
10(1):
50 - 69.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
C. D. MARTIN
More Than the Work: Race and Gender Differences in Caregiving Burden
Journal of Family Issues,
November 1, 2000;
21(8):
986 - 1005.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
R. J. V. Montgomery
The Family Role in the Context of Long-Term Care
J Aging Health,
August 1, 1999;
11(3):
383 - 416.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
L. Levesque, F. Ducharme, L. Lachance, L. A. Gerdner, M. M. Jirovec, and L. Levesque
Is there a Difference between Family Caregiving of Institutionalized Elders with or without Dementia?
West J Nurs Res,
August 1, 1999;
21(4):
472 - 497.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
C. W. Peek, B. A. Zsembik, and R. T. Coward
The Changing Caregiving Networks of Older Adults
Research on Aging,
September 1, 1997;
19(3):
333 - 361.
[Abstract]
|
 |
|

|
 |

|
 |
 
V. Braithwaite
Understanding Stress in Informal Caregiving: Is Burden a Problem of the Individual or of Society?
Research on Aging,
June 1, 1996;
18(2):
139 - 174.
[Abstract]
|
 |
|

|
 |

|
 |
 
D. Ward, M. A. Brown, and V. R. Strang
Labor and Cost in AIDS Family Caregiving
West J Nurs Res,
February 1, 1994;
16(1):
10 - 25.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Spitze and J. R. Logan
Helping as a Component of Parent-Adult Child Relations
Research on Aging,
September 1, 1992;
14(3):
291 - 312.
[Abstract]
|
 |
|

|
 |

|
 |
 
V. Braithwaite
Caregiving Burden: Making the Concept Scientifically Useful and Policy Relevant
Research on Aging,
March 1, 1992;
14(1):
3 - 27.
[Abstract]
|
 |
|
|
|