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首页> 外文期刊>Psycho-Oncology: Journal of the Psychological Social and Behavioral Dimensions of Cancer >Psychological distress among family carers of oesophageal cancer survivors: the role of illness cognitions and coping.
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Psychological distress among family carers of oesophageal cancer survivors: the role of illness cognitions and coping.

机译:食道癌幸存者家庭照顾者的心理困扰:疾病认知和应对的作用。

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摘要

Objective: The research aimed to determine the extent to which illness cognitions and coping explain psychological distress (fear of cancer recurrence, anxiety and depression symptoms) among family carers of survivors of oesophageal cancer. Methods: Carers of patients registered with the Oesophageal Patients' Association in the UK were mailed a questionnaire booklet containing questions about medical and demographic variables, the Illness Perception Questionnaire-Revised, the Cancer Coping Questionnaire, the Concerns about Recurrence Scale and the Hospital Anxiety and Depression Scale. Results: Complete responses were received from 382 family carers (75% male; mean (SD) age=62 (10.91) years). Regression models indicated that the variables measured could explain between 35 and 49% of the variance in psychological distress among carers. Illness cognitions (particularly perceptions of the cause of, consequences of and personal control over oesophageal cancer and the carer's understanding of the condition) explained the majority of this variance. Positive focus coping strategies were also found to be important in explaining psychological distress. Conclusion: The results of this study are consistent with previous research demonstrating that illness cognitions are significant correlates of adaptive outcomes, thereby suggesting that cognition-based interventions could potentially be effective in minimizing emotional distress among family carers of oesophageal cancer survivors. Copyright (c) 2010 John Wiley & Sons, Ltd.
机译:目的:该研究旨在确定食道癌幸存者家庭照顾者的疾病认知和应对方式解释心理困扰(对癌症复发,焦虑和抑郁症状的恐惧)的程度。方法:向在英国食管患者协会注册的患者的护理人员邮寄了一份调查问卷小册子,其中包含有关医学和人口统计学变量,疾病知觉问卷的修订版,癌症应对问卷,对复发量表的关注以及医院焦虑症和抑郁量表。结果:382名家庭护理人员(75%的男性;平均(SD)年龄= 62(10.91)岁)收到了完整的答复。回归模型表明,所测量的变量可以解释护理人员心理困扰变化的35%至49%。疾病认知(尤其是对食道癌的原因,后果和对人的控制以及护理人员对病情的理解)解释了这种差异的大部分。还发现积极的焦点应对策略在解释心理困扰方面也很重要。结论:本研究结果与先前的研究一致,表明疾病认知与适应性结局具有显着相关性,从而表明基于认知的干预措施可能有效地减少食道癌幸存者家庭护理人员的情绪困扰。版权所有(c)2010 John Wiley&Sons,Ltd.

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