In recent years there has been a growing body of literature
regarding the experiences and well-being of people providing care to
a relative with dementia. There is some evidence within this
literature that sub-groups of caregivers respond differently to the
caregiving situation. In particular, findings have tended to
suggest that women caregivers experience more burden and distress
than men ( eg Gilhooly, 1984a; Gilleard et al , 1984) , and that
spouses of the care recipient experience more burden and distress as
carers than children (eg George & Gwyther, 1986; Gilhooly, 1984a).
Various explanations have been postulated, one of which focuses on
caregivers' expectations of themselves in providing care: it has
been speculated that women may have higher expectations of
themselves (eg Schnoover et al, 1988), due to a sense that in
providing care they are fulfilling an appropriate or anticipated
role. It is suggested here that a similar argument may be extended
to spousal caregivers.
This study, then, aimed to investigate the levels of expectation of
27 caregivers, and any role this factor may play in determining
levels of burden and distress. Differences between the expectations
of women and men, and spousal and child caregivers were also
investigated, as was the effect of expectations on the use of social
support.
Contrary to hypotheses, it was found that expectation levels were
inversely related to levels of burden, and there were no differences
between sub-groups. There was evidence of differentia1use of
support for caregivers with different levels of expectation: those
with higher expectations of themselves reporting the availability of
more informal supports, but lower frequency of contact with services
than those with lower expectations.
The results provide a characterisation of the more burdened
caregivers being those who have lower expectations of themselves to
provide care, who are less involved in caregiving and receive more
support in the role. Potential explanations for these findings are
discussed, limitations imposed by the methodology of the study are
outlined and clinical implications of the present results are
considered,
Date of Award | 1993 |
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Original language | English |
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Awarding Institution | |
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THE ROLE OF EXPECTATIONS IN DETERMINING CAREGIVER WELL-BEING
Foote, K. J. (Author). 1993
Student thesis: PhD