Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/248908
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dc.titleCaring for persons with schizophrenia at home: examining the link between family caregivers' role distress and quality of life
dc.contributor.authorQuah, Stella
dc.date.accessioned2024-06-14T07:55:55Z
dc.date.available2024-06-14T07:55:55Z
dc.date.issued2014-05
dc.identifier.citationQuah, Stella (2014-05). Caring for persons with schizophrenia at home: examining the link between family caregivers' role distress and quality of life. SOCIOLOGY OF HEALTH & ILLNESS 36 (4) : 596-612. ScholarBank@NUS Repository.
dc.identifier.issn0141-9889
dc.identifier.issn1467-9566
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/248908
dc.description.abstractThis article re-examines the link between role distress and quality of life of family caregivers of a loved one with schizophrenia by exploring the impact of role overload (defined as spending 7 or more hours daily looking after the care recipient). Role theory and symbolic interactionism provide the conceptual background to this study. The research question is: under what conditions does role distress reduce quality of life? The answer helps us identify circumstances under which caregivers may be able to carry out their stressful caregiving role while minimising a decline in their quality of life. The data are from a purposive sample of 47 family caregivers in Singapore who were interviewed in person using a semi-structured questionnaire. The data analysis includes non-parametric tests, exploratory factor analysis and relative risks estimates. The findings show that the inverse association between role distress and quality of life found in most studies of family caregivers changes when hours of care are taken into consideration. While role distress is found among all family caregivers it only reduces the family caregiver's quality of life in situations of role overload. The implications for the situation of family caregivers are discussed. © 2013 Foundation for the Sociology of Health & Illness/John Wiley & Sons Ltd.
dc.language.isoen
dc.publisherWILEY
dc.sourceElements
dc.subjectScience & Technology
dc.subjectSocial Sciences
dc.subjectLife Sciences & Biomedicine
dc.subjectPublic, Environmental & Occupational Health
dc.subjectSocial Sciences, Biomedical
dc.subjectSociology
dc.subjectBiomedical Social Sciences
dc.subjectrole distress
dc.subjectschizophrenia
dc.subjectfamily caregivers
dc.subjectrole overload
dc.subjectquality of life
dc.subjectculture
dc.subjectMENTAL-HEALTH-SERVICES
dc.subjectBIPOLAR DISORDER
dc.subjectSAMPLE-SIZE
dc.subjectBURDEN
dc.subjectSUPPORT
dc.subjectINTERVENTION
dc.subjectCOERCION
dc.subjectPEOPLE
dc.subjectMODELS
dc.subjectSTRAIN
dc.typeArticle
dc.date.updated2024-06-11T03:55:25Z
dc.contributor.departmentDEAN'S OFFICE (DUKE-NUS MEDICAL SCHOOL)
dc.description.sourcetitleSOCIOLOGY OF HEALTH & ILLNESS
dc.description.volume36
dc.description.issue4
dc.description.page596-612
dc.published.statePublished
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