Needs analysis of family caregivers of people living with dementia in Sleman Regency, Yogyakarta.

Wikan Ardiningrum, Martina Wiwie Setiawan Nasrun, Profitasari Kusumaningrum, Charles Evert Damping
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Abstract

Background: Without appropriate support, taking care of people living with dementia may become a burden for family caregivers. Identifying the needs for caregivers can help them minimise the burden of caring and meet quality care for people living with dementia.

Methods: In the first phase, a content validity test was conducted on the Carers' Needs Assessment of Dementia (CNA-D) in the Indonesian version. The second phase, a sequential explanatory mixed-methods design, was conducted on 65 family caregivers in two stages. The first stage was a cross-sectional study. A correlation test between caregiver problems and caregiver burden was conducted. The caregiver problems that were statistically significant were analyzed to reveal the unmet needs. A needs analysis was also conducted on problems experienced by more than half of the caregivers. In the second stage, we conducted a semi-structured individual interview, and thematic analysis was used to analyze the data.

Results: The result of the validity test of the CNA-D instrument, Indonesian version, obtained a high value for content validity. The main problem of caregivers is a lack of information about dementia; however, it does not have a significant correlation with caregiver burden. The caregiver problem with the highest correlation to caregiver burden is burnout due to caring. More than 50% of caregivers' needs in Sleman Regency were not met in this research. The most essential needs that were not met were counselling and psychotherapy (83.3%-92%). The personal understanding of dementia, spiritual values in caring, cultural values in caring, barriers to accessing healthcare services, and self-care strategies should be considered in fulfilling family caregiver needs.

Conclusion: Most of the needs of family caregivers of people living with dementia in Sleman Regency, Yogyakarta, have not been met. Therefore, it requires collaboration with multi-professionals and all stakeholders to fulfil these needs.

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日惹 Sleman 地区痴呆症患者家庭照顾者的需求分析。
背景:如果没有适当的支持,照顾痴呆症患者可能会成为家庭照顾者的负担。确定照护者的需求可以帮助他们最大限度地减轻照护负担,并为痴呆症患者提供高质量的护理:第一阶段,对印尼语版痴呆症照护者需求评估(CNA-D)进行了内容有效性测试。第二阶段采用顺序解释混合方法设计,分两个阶段对 65 名家庭照护者进行了调查。第一阶段为横断面研究。对照顾者的问题和照顾者的负担进行了相关性测试。对统计学意义显著的照顾者问题进行分析,以揭示未满足的需求。我们还对半数以上照顾者遇到的问题进行了需求分析。在第二阶段,我们进行了半结构化的个别访谈,并采用主题分析法对数据进行了分析:结果:印尼版 CNA-D 工具的效度测试结果显示,其内容效度值较高。照护者的主要问题是缺乏有关痴呆症的信息,但这一问题与照护者的负担没有明显的相关性。与照顾者负担相关性最高的照顾者问题是因照顾而产生的职业倦怠。在这项研究中,Sleman Regency 50%以上的照护者需求没有得到满足。未得到满足的最基本需求是咨询和心理治疗(83.3%-92%)。在满足家庭照护者的需求时,应考虑到个人对痴呆症的理解、照护中的精神价值、照护中的文化价值、获得医疗服务的障碍以及自我照护策略:结论:日惹苏莱曼县大多数痴呆症患者家庭护理者的需求尚未得到满足。因此,需要与多方专业人士和所有利益相关者合作,以满足这些需求。
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