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Burden and coping strategies experienced by caregivers of persons with schizophrenia in the community

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Listed:
  • Sharon CH Tan
  • Ai Lean Yeoh
  • Irene BK Choo
  • Adeline PH Huang
  • Seng Hong Ong
  • Hafizah Ismail
  • Pei Pei Ang
  • Yiong Huak Chan

Abstract

Aims and objectives. Examined the levels of burden and the coping strategies experienced by caregivers of persons with schizophrenia in the community. It aims (1) to provide mental healthcare professionals with more information about caregiver stressors and (2) to recommend more effective community resources and support. Background. A caregiver’s burden increases due to negative coping skills and lack of resources. However, insufficient studies of caregiver burden and coping skills accentuate the already inadequate understanding of the field. This lack of understanding often leads to frequent readmission of patients when caregivers give up their care‐giving responsibilities. Design. Descriptive and quantitative methods. Methods. Convenience sampling method was used at three outpatient clinics on 150 caregivers. The Burden Assessment Scale measured care‐giving burden. The Family Crisis‐Oriented Personal Scales examined the coping strategies. Results. Findings reveal that 31·3% caregivers felt distress and 33·3% found stigma upsetting. Only 14·7% sought help from healthcare workers and 49·3% were interested to know more. Nevertheless, 24·7% verbalized sufficient social support. Conclusions. Results demonstrated a high burden on caregivers because of many factors such as other commitments, lack of resources, insufficient financial support, education level and ageing. This study found that long‐term caregivers suffer more than short‐term ones, which is contrary to Seng’s study (2005). Burden increases further for those having to cope with both work and care giving at the same time. Relevance to clinical practice. It is critical to improve and increase services and resources to support care giving. It is also essential to educate and ensure that the people affected know how to leverage the available resources. It is important to improve and increase our services and resources. It is also essential to educate and ensure the people concerned know how to make use of them. It also essential to educate and ensure the people concerned know how to make use of them.

Suggested Citation

  • Sharon CH Tan & Ai Lean Yeoh & Irene BK Choo & Adeline PH Huang & Seng Hong Ong & Hafizah Ismail & Pei Pei Ang & Yiong Huak Chan, 2012. "Burden and coping strategies experienced by caregivers of persons with schizophrenia in the community," Journal of Clinical Nursing, John Wiley & Sons, vol. 21(17‐18), pages 2410-2418, September.
  • Handle: RePEc:wly:jocnur:v:21:y:2012:i:17-18:p:2410-2418
    DOI: 10.1111/j.1365-2702.2012.04174.x
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    Cited by:

    1. Farnaz Rahmani & Hossein Ebrahimi & Naeimeh Seyedfatemi & Hossein Namdar Areshtanab & Fatemeh Ranjbar & Bill Whitehead, 2018. "Trapped like a butterfly in a spider's web: Experiences of female spousal caregivers in the care of husbands with severe mental illness," Journal of Clinical Nursing, John Wiley & Sons, vol. 27(7-8), pages 1507-1518, April.
    2. Man-Man Peng & Jianli Xing & Xinfeng Tang & Qinglu Wu & Dannuo Wei & Mao-Sheng Ran, 2022. "Disease-Related Risk Factors for Caregiver Burden among Family Caregivers of Persons with Schizophrenia: A Systematic Review and Meta-Analysis," IJERPH, MDPI, vol. 19(3), pages 1-16, February.
    3. Jui‐Fen Cheng & Xuan‐Yi Huang & Mei‐Jue Lin & Ya‐Hui Wang & Tzu‐Pei Yeh, 2018. "The influence of a mental health home visit service partnership intervention on the caregivers’ home visit service satisfaction and care burden," Journal of Clinical Nursing, John Wiley & Sons, vol. 27(3-4), pages 668-677, February.

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