Experiences of stigma and discrimination faced by family caregivers of people with schizophrenia in India
Опыт стигматизации и дискриминации, с которыми сталкиваются семейные лица, осуществляющие уход за людьми с шизофренией, в Индии
2017-02-01
SCID: 54.1/vqwzkqxs
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Abstract (AI)
Stigma associated with schizophrenia significantly affects family caregivers, yet few studies have examined the nature and determinants of family stigma and its relationship to their knowledge about the condition. This paper describes the experiences and determinants of stigma reported by the primary caregivers of people living with schizophrenia (PLS) in India. The study used mixed methods and was nested in a randomised controlled trial of community care for people with schizophrenia. Between November 2009 and October 2010, data on caregiver stigma and functional outcomes were collected from a sample of 282 PLS-caregiver dyads. In addition, 36 in-depth-interviews were conducted with caregivers. Quantitative findings indicate that 'high caregiver stigma' was reported by a significant minority of caregivers (21%) and that many felt uncomfortable to disclose their family member's condition (45%). Caregiver stigma was independently associated with higher levels of positive symptoms of schizophrenia, higher levels of disability, younger PLS age, household education at secondary school level and research site. Knowledge about schizophrenia was not associated with caregiver stigma. Qualitative data illustrate the various ways in which stigma affected the lives of family caregivers and reveal relevant links between caregiver-stigma related themes ('others finding out', 'negative reactions' and 'negative feelings and views about the self') and other themes in the data. Findings highlight the need for interventions that address both the needs of PLS and their family caregivers. Qualitative data also illustrate the complexities surrounding the relationship between knowledge and stigma and suggest that providing 'knowledge about schizophrenia' may influence the process of stigmatisation in both positive and negative ways. We posit that educational interventions need to consider context-specific factors when choosing anti-stigma-messages to be conveyed. Our findings suggest that messages such as 'recovery is possible' and 'no-one is to blame' may be more helpful than focusing on bio-medical knowledge alone.
Key Findings
1
A significant minority of caregivers reported high stigma (21%), while 45% felt uncomfortable disclosing their family member’s schizophrenia.
2
Anti-stigma interventions should address patients and caregivers together, use context-specific messages, and potentially emphasize recovery and shared non-blame rather than biomedical knowledge alone.
3
Caregiver stigma was independently associated with more severe positive symptoms, greater disability, younger patient age, secondary-level household education, and research site.
4
Knowledge about schizophrenia was not associated with caregiver stigma in quantitative analyses.
5
Qualitative interviews showed that stigma affected caregivers through fear of disclosure, negative reactions from others, and negative self-feelings.
Research Object
Family caregivers of people living with schizophrenia in India
Research Subject
Experiences, determinants, and knowledge-related aspects of caregiver stigma and discrimination
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2017-02-01
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