The lived experiences of caregivers: psychological and social implications of caring for patients with Bipolar Disorder

dc.contributor.authorNicolau, Mikaela Diane
dc.contributor.supervisorKasese-Hara, Mambwe
dc.date.accessioned2024-08-08T15:04:21Z
dc.date.available2024-08-08T15:04:21Z
dc.date.issued2023-05
dc.departmentDepartment of Psychology
dc.descriptionA Research Report Submitted in partial fulfilment of the requirements for the Degree of Master of Arts in Social and Psychological Research (PSYC7022) in the Department of Psychology, School of Human and Community Development, Faculty of Humanities, at the University of the Witwatersrand, Johannesburg, 2023.
dc.description.abstractDue to the nature of the illness, bipolar disorder (BD) has detrimental effects on the diagnosed patients as well as their caregivers (Hajda et al., 2016). Vast amounts of research have been published on the impact and implications experienced by caregivers of mentally ill patients however, a majority of research assessing the psychological and socio-economic status of the caregivers has been quantitative in nature (Sharif et al., 2020). This study sought to understand the psychological and social implications of caring for a patient with BD, with a specific focus on caregivers in the Gauteng region. The middle-class was chosen as Ayalew et al. (2019) found that the higher the caregiver’s income, the fewer implications they experienced as a caregiver. A phenomenological framework was used to conduct this study. The qualitative method of data collection was face-to-face, in-depth interviews with six participants (two males, four females), who were selected using purposive sampling. The interviews were transcribed verbatim, and the data analysed by means of Interpretative Phenomenological Analysis. For the caregivers in the current study, managing the patient’s unpredictable behaviour and dealing with the varying symptoms of the disorder presented a challenge. They described the caregiving role as an emotional rollercoaster, signifying the chaotic, up-and-down nature of the disorder. Being a mother-caregiver led to shared experiences among the caregivers, with similar implications being expressed. Being a wife, however, presented significantly greater caregiver implications. The male caregivers have adapted to their roles better than the females. The theme of financial implications was interesting in this study, as these implications varied among the respondents. The researcher found it interesting that five of the participants spoke about neglecting their needs without any probing, yet they also acknowledged the importance of self-care and being aware of their mental state. The participants in this study expressed the need for support groups, which are lacking in the country. Whilst the findings of this study were in line with much published research, the researcher notes that there is a scarcity of literature covering some of the themes and subthemes presented, and therefore further research should be conducted.
dc.description.submitterMM2024
dc.facultyFaculty of Humanities
dc.identifier.citationNicolau, Mikaela Diane. (2023). The lived experiences of caregivers: psychological and social implications of caring for patients with Bipolar Disorder. [Master's dissertation, University of the Witwatersrand, Johannesburg]. WIReDSpace. https://hdl.handle.net/10539/40048
dc.identifier.urihttps://hdl.handle.net/10539/40048
dc.language.isoen
dc.publisherUniversity of the Witwatersrand, Johannesburg
dc.rights©2023 University of the Witwatersrand, Johannesburg. All rights reserved. The copyright in this work vests in the University of the Witwatersrand, Johannesburg. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of University of the Witwatersrand, Johannesburg.
dc.rights.holderUniversity of the Witwatersrand, Johannesburg
dc.schoolSchool of Human and Community Development
dc.subjectCaregiver
dc.subjectPsychological
dc.subjectSocial
dc.subjectImplications
dc.subjectBipolar disorder
dc.subjectGauteng
dc.subjectMiddle-class
dc.subjectUCTD
dc.subject.otherSDG-3: Good health and well-being
dc.titleThe lived experiences of caregivers: psychological and social implications of caring for patients with Bipolar Disorder
dc.typeDissertation

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