Abstract
Services have been increasingly directed at supporting carers of people living with mental illness but it is difficult to evaluate the impact of service change where benchmarks for carer functioning are sparse. Sixty Australian carers were assessed regarding their quality of life, psychological distress, social isolation and caregiving experience. Their scores were compared with two matched community samples and previous studies. Carers were ten times more likely to be socially isolated and quality of life was significantly less than matched community samples. Over 40 % of the carer sample met criteria for probable psychiatric disorder. Comparison of caregiving experiences with a study 15 years ago showed no improvement in negative caregiving experiences. Carers still face considerable challenges to their wellbeing as they support people living with mental illness, in spite of progress in the development of policy and services.
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Acknowledgments
Sadly, our colleague Associate Professor Graeme Hawthorne passed away in 2014 and we would like to acknowledge his contribution to this paper and to the Building Family Skills Together Research Group. We would also like to acknowledge the William Buckland Foundation for their support of this research and the contributions of the other Building Family Skills Together Research Group members, Assoc Prof Amaryll Perlesz and Dr Peter McKenzie and Family WorkNet members, Jenny Burger and Dr Margaret Leggatt. A special thank you is extended to the consumers and carers who generously contributed their time and expertise to the research and shared their experiences with honesty, integrity and dignity and their case managers who assisted with recruitment.
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The research presented in this article has been approved by the relevant ethics committee and conforms to the provisions of the Declaration of Helsinki (1995, revised Edinburgh, 2000). All participants in the research gave informed consent and patient anonymity has been preserved.
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Hayes, L., Hawthorne, G., Farhall, J. et al. Quality of Life and Social Isolation Among Caregivers of Adults with Schizophrenia: Policy and Outcomes. Community Ment Health J 51, 591–597 (2015). https://doi.org/10.1007/s10597-015-9848-6
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DOI: https://doi.org/10.1007/s10597-015-9848-6