Researching the social aspects of dementia from a social work perspective

Jana Mali, Ana Štambuk
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Abstract

The issues associated with dementia are challenging for social workers, who have a lot of direct contact with people with dementia, as well as their support networks. These networks play a key role in the care of people with dementia. Social workers differ from other professionals in that they are aware of the urgency of attending to social justice, as well as the implementation of human rights, participation and equality. Recognising the experiences of people with dementia is of paramount relevance to social work, as it provides insight into their needs and the aptness of existing forms of assistance in responding to their needs. Through this approach, those working in social work strive to find new forms of help to enable people with dementia to live independently in their community. It is important to find ways to involve people with dementia as active co-creators in the helping process and in exploring the social perspectives of dementia. In the present paper, we present the literature review on experience of researching dementia from a social work perspective in Slovenia and Croatia—two countries with similarities in the development of social work and its research. The inclusion of people with Alzheimer's disease or dementia in research is very complex. Both professionals working with people with dementia (formal caregivers) and family members (mostly informal caregivers) face various difficulties and pressures. It is therefore important to consider research ethics and respect existing legal frameworks and informed consent. An individualised approach should be used to include people with dementia in research to meet their need for personal worth and dignity (despite numerous mental and functional deficits). Ultimately, all research should strive to determine the true situation of people with dementia and their needs, with the aim of using and developing their remaining abilities to improve the quality of life for both those people and those who provide care for them.
从社会工作角度研究老年痴呆症的社会问题
与痴呆症相关的问题对社会工作者来说具有挑战性,因为他们与痴呆症患者及其支持网络有很多直接接触。这些网络在照顾痴呆症患者的过程中发挥着关键作用。社工与其他专业人员的不同之处在于,他们意识到关注社会正义以及落实人权、参与和平等的紧迫性。认识到痴呆症患者的经历对社会工作至关重要,因为这有助于深入了解他们的需求以及现有的援助形式是否能够满足他们的需求。通过这种方法,社会工作者努力寻找新的帮助方式,使痴呆症患者能够在社区中独立生活。重要的是要找到方法,让痴呆症患者作为积极的共同创造者参与到帮助过程中,并探索痴呆症的社会视角。在本文中,我们对斯洛文尼亚和克罗地亚从社会工作角度研究痴呆症的经验进行了文献综述,这两个国家在社会工作及其研究的发展方面有着相似之处。将阿尔茨海默氏症或痴呆症患者纳入研究工作非常复杂。与痴呆症患者打交道的专业人员(正式护理人员)和家庭成员(主要是非正式护理人员)都面临着各种困难和压力。因此,考虑研究伦理、尊重现有法律框架和知情同意非常重要。应采用个性化的方法让痴呆症患者参与研究,以满足他们对个人价值和尊严的需求(尽管他们存在诸多精神和功能障碍)。归根结底,所有研究都应努力确定痴呆症患者的真实情况及其需求,目的是利用和发展他们的剩余能力,提高患者和护理人员的生活质量。
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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