Abstract
The purpose of this study was to describe how HIV informal caregivers experience the social and biophysical dimensions of the HIV illness process and develop a supportive and sustaining environment. The specific aims of this project were to: (1) explore the role responsibilities of HIV/AIDS informal caregivers over the course of HIV illness; and (2) describe the effect of a case management model on HIV/AIDS informal caregivers' health/well-being and satisfaction with formal services. A prospective design was used to facilitate exploration of the emergent nature of the caregiving role. Data was gathered in 32 indepth interviews with 20 subjects who were the primary caregivers to individuals manifesting HIV/AIDS. The interviews, guided by a semi-structured interview format, were audiotaped and transcribed. Data was coded and thematically analyzed using interpretative techniques. A randomized portion of the sample received case managed services and its effects were evaluated with standardized outcome measures of health/well-being and satisfaction with formal services. HIV informal caregiving was analyzed as a three phase process. The first phase of HIV informal caregiving, beginning the role, involves decisions to assume the role and issues to be negotiated as the caregiver adapts to the altered patient-caregiver relationship. The second phase, sustaining the role, centers on matters of identity building and the aspects of managing the role in relation to performing patient centered activities; managing courtesy stigma; living with loss and sorrow; and minimizing exposure to the virus. The last phase of the role, ending the role, involves the processes by which caregivers may relinquish their role prematurely as a means of minimizing role conflict/overload and the grief and bereavement processes that occur following patient death. The major role responsibility for HIV informal caregivers that occurred over the three phases was finding "balance," a process by which the caregiver sought to secure coherence and equilibrium between several interacting and often opposing processes in which they were engaged. Development of the HIV informal caregiver role was found to be particularly intricate because HIV informal caregiver role expectations are complicated by the unusual social meanings surrounding AIDS and gay relationships. It was not established that case management effected HIV informal caregiver health/well-being and satisfaction with formal services.
Sigma Membership
Nu Beta at-Large
Type
Dissertation
Format Type
Text-based Document
Study Design/Type
Other
Research Approach
Mixed/Multi Method Research
Keywords:
HIV Caregivers' Experiences, Patient-Caregiver Relationships, Patient Case Management
Advisors
Anderson, Carole A.
Advisor
Carole A. Anderson
Degree
PhD
Degree Grantor
The Ohio State University
Degree Year
1993
Recommended Citation
Reynolds, Nancy R., "HIV informal caregiving: Role responsibilities and the effects of case management" (2019). Dissertations. 1246.
https://www.sigmarepository.org/dissertations/1246
Rights Holder
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Review Type
None: Degree-based Submission
Acquisition
Proxy-submission
Date of Issue
2019-09-10
Full Text of Presentation
wf_yes
Description
This dissertation has also been disseminated through the ProQuest Dissertations and Theses database. Dissertation/thesis number: 9401340; ProQuest document ID: 304085225. The author still retains copyright.