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The Role of Social Location in Copin...
~
Ragin, Jacqueline.
The Role of Social Location in Coping with Caregiving.
紀錄類型:
書目-語言資料,手稿 : Monograph/item
正題名/作者:
The Role of Social Location in Coping with Caregiving./
作者:
Ragin, Jacqueline.
面頁冊數:
1 online resource (135 pages)
附註:
Source: Dissertation Abstracts International, Volume: 79-03(E), Section: A.
Contained By:
Dissertation Abstracts International79-03A(E).
標題:
Sociology. -
電子資源:
click for full text (PQDT)
ISBN:
9780355312393
The Role of Social Location in Coping with Caregiving.
Ragin, Jacqueline.
The Role of Social Location in Coping with Caregiving.
- 1 online resource (135 pages)
Source: Dissertation Abstracts International, Volume: 79-03(E), Section: A.
Thesis (Ph.D.)
Includes bibliographical references
A salient concern stemming from population aging is the expected rise in demand for informal family caregivers for diseases impacting the elderly, including dementia (MMMI 2010; NIA and WHO 2011). Studies of caregiver well-being often problematize the sociodemographic caregivers (e.g. gender, marital status) while caregiver intervention studies typically focus on the program itself (Gallagher-Thompson et al., 2008; Rabinowitz et al., 2006; Shulz et al., 2003). In this dissertation I unite these two bodies of caregiver research and examine how the sociodemographic characteristics of participants in a caregiver intervention program relate to the program's effectiveness. I use secondary data from the Stress Management Project Dataset (Spiegel, 2001) and evaluate how participants' social location (specifically, race and education) impacts the effectiveness of each program on caregivers' depressive symptoms and stress. This study employed a sociological perspective to examine how social location (specifically race and education) impacts the benefits of a dementia caregiver intervention program. Using secondary data, I performed OLS regression analyses and found support for the initial hypothesis that suggested that the Coping with Caregiving (CWC) intervention would be more effective than the Telephone Support Control (TSC). There was no support for the remaining hypotheses that proposed that White caregivers with more education would benefit more from the program, or that the effects of race and education on caregiver outcomes would be contingent upon each other.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2018
Mode of access: World Wide Web
ISBN: 9780355312393Subjects--Topical Terms:
551705
Sociology.
Index Terms--Genre/Form:
554714
Electronic books.
The Role of Social Location in Coping with Caregiving.
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A salient concern stemming from population aging is the expected rise in demand for informal family caregivers for diseases impacting the elderly, including dementia (MMMI 2010; NIA and WHO 2011). Studies of caregiver well-being often problematize the sociodemographic caregivers (e.g. gender, marital status) while caregiver intervention studies typically focus on the program itself (Gallagher-Thompson et al., 2008; Rabinowitz et al., 2006; Shulz et al., 2003). In this dissertation I unite these two bodies of caregiver research and examine how the sociodemographic characteristics of participants in a caregiver intervention program relate to the program's effectiveness. I use secondary data from the Stress Management Project Dataset (Spiegel, 2001) and evaluate how participants' social location (specifically, race and education) impacts the effectiveness of each program on caregivers' depressive symptoms and stress. This study employed a sociological perspective to examine how social location (specifically race and education) impacts the benefits of a dementia caregiver intervention program. Using secondary data, I performed OLS regression analyses and found support for the initial hypothesis that suggested that the Coping with Caregiving (CWC) intervention would be more effective than the Telephone Support Control (TSC). There was no support for the remaining hypotheses that proposed that White caregivers with more education would benefit more from the program, or that the effects of race and education on caregiver outcomes would be contingent upon each other.
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