Experiences of Informal Caregivers Facing Cancer While Caring for Someone With Dementia: Qualitative Interview Study.

IF 2.6 Q2 ONCOLOGY
JMIR Cancer Pub Date : 2026-10-05 DOI:10.2196/93688
Elizabeth Travis, Mollie Louise Price, Millie Slessor, Jacqueline Crewe, Laura Ashley
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Abstract

Background: Informal caregivers play a fundamental role in the diagnosis, treatment, and care received by their family members. Caring for someone with dementia is particularly burdensome and can have negative effects on caregivers' health. Despite caregivers being widely recognized as vulnerable, the psychosocial needs of caregivers who are managing cancer themselves remain unknown.

Objective: This study aims to investigate the experiences of UK family caregivers who have received a cancer diagnosis while caring for someone with dementia or memory problems.

Methods: Twenty-five UK informal family caregivers who had received a cancer diagnosis were recruited through convenience sampling to take part in in-depth semistructured interviews. The interviews explored participants' experiences of managing cancer alongside dementia caregiving, including the impact on treatment and caregiving, emotional challenges, support needs, and experiences of formal and informal support. Ethical approval was obtained from the Leeds Beckett University Research Ethics Committee, and all participants provided informed consent. Reflexive thematic analysis was conducted.

Results: Three key themes were identified: (1) caring responsibilities can complicate and take priority over cancer care, (2) caregiving can intensify cancer-related distress and anxieties, and (3) managing cancer while caring increases the need for support and coping resources. For dementia caregivers, having cancer can surface/heighten feelings of predeath grief and worries about future care planning for their care recipient. Dementia caregivers viewed multifaceted social support as vital for enabling access to and coping with cancer treatment.

Conclusions: Dementia caregivers who are also living with cancer continue to shoulder the burden of illness work on behalf of their care recipients while simultaneously managing their own cancer diagnosis and treatment. Caregiving responsibilities often take priority over cancer care, intensify the practical and emotional challenges of cancer, and increase the need for and reliance on support resources. These findings highlight the need for person-centered adjustments to cancer care, dementia-friendly health care environments, and tailored psycho-oncology support that address the practical and emotional needs of dementia caregivers.

非正式照护者在照顾痴呆症患者时面对癌症的经验:质性访谈研究。
背景:非正式照顾者在其家庭成员的诊断、治疗和护理中发挥着重要作用。照顾痴呆症患者是一项特别繁重的工作,并可能对护理者的健康产生负面影响。尽管人们普遍认为护理人员是弱势群体,但对癌症患者本身的心理社会需求仍不甚了解。目的:本研究旨在调查英国家庭照顾者在照顾患有痴呆症或记忆问题的人时接受癌症诊断的经历。方法:通过方便抽样的方法,招募了25名英国非正式家庭护理人员,他们接受了癌症诊断,参加了深入的半结构化访谈。访谈探讨了参与者管理癌症和痴呆症护理的经历,包括对治疗和护理的影响、情感挑战、支持需求以及正式和非正式支持的经历。获得利兹贝克特大学研究伦理委员会的伦理批准,所有参与者都提供了知情同意。进行反身性主题分析。结果:确定了三个关键主题:(1)照顾责任会使癌症护理复杂化并优先于癌症护理;(2)照顾会加剧癌症相关的痛苦和焦虑;(3)在照顾癌症的同时管理癌症增加了对支持和应对资源的需求。对于痴呆症护理人员来说,患癌症会加剧临终前的悲伤情绪,并对他们的护理对象的未来护理计划感到担忧。痴呆症护理人员认为,多方面的社会支持对于获得和应对癌症治疗至关重要。结论:患有癌症的痴呆症护理人员在管理自己的癌症诊断和治疗的同时,继续代表他们的护理对象承担疾病工作的负担。照顾责任往往优先于癌症护理,加剧了癌症的实际和情感挑战,并增加了对支持资源的需求和依赖。这些发现强调了以人为中心调整癌症护理的必要性,痴呆症友好的卫生保健环境,以及量身定制的心理肿瘤学支持,以满足痴呆症护理者的实际和情感需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JMIR Cancer
JMIR Cancer ONCOLOGY-
CiteScore
4.10
自引率
0.00%
发文量
64
审稿时长
12 weeks
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