Fan Qiping, DuBose Logan, Ory Marcia G, Lee Shinduk, Hoang Minh-Nguyet, Vennatt Jeswin, Kew Chung Lin, Doyle David, Falohun Tokunbo
Department of Health Behavior, School of Public Health, Texas A&M University, College Station, TX, United States.
Department of Public Health Sciences, Clemson University, Clemson, SC, United States.
JMIR Aging. 2023 Sep 5;6:e47577. doi: 10.2196/47577.
Alzheimer disease and Alzheimer disease-related dementia represent complex neuropathologies directly challenging individuals, their families, and communities in the United States. To support persons living with dementia, family or informal caregivers often encounter complex financial, psychological, and physical challenges. A widely used solution such as a consolidated web-based assistance or guidance platform is missing, compounding care challenges.
In preparation for designing an internet-based artificial intelligence-driven digital resource platform, a qualitative interview study was conducted to characterize the challenges and needs of family caregivers in the United States.
A semistructured interview topic guide in English was developed by engaging community partners and research partnerships. Family caregiver participants were purposefully recruited via various means, such as word of mouth, local dementia community service providers, digital recruitment emails, flyers, and social media. Interested individuals were first invited to complete an eligibility screening survey, and eligible individuals were then contacted to arrange a web-based in-depth interview via Zoom (Zoom Video Communications) from January 1, 2022, to May 31, 2022. A follow-up survey was administered in May 2022 to provide an overview of the participants' demographics, socioeconomic characteristics, and caregiving information. Thematic analysis in a framework approach was used to identify and organize themes and the study findings.
Following the prescreening of 150 eligible respondents, 20% (30/150) individuals completed both the interviews and follow-up survey, allowing for an in-depth look into the challenges, experiences, and expectations of primary caregivers of people living with dementia. Most participants (20/30, 67%) were primary caregivers of persons with dementia, and 93% (28/30) had provided care for at least a year. Most participants were aged >50 years (25/30, 83%), female (23/30, 77%), White (25/30, 83%), and non-Hispanic (27/30, 90%) and held a bachelor's or graduate degree (22/30, 73%). Collectively, all participants acknowledged challenges in caring for people living with dementia. Thematic analyses elicited the challenges of caregiving related to functional care needs and financial and legal challenges. In addition, participants identified the need for an integrative digital platform where information could be supplied to foster education, share resources, and provide community support, enabling family caregivers to improve the quality of care and reducing caregiver burden.
This study emphasized the difficulties associated with the family caregiver role and the expectations and potential for a supportive web-based platform to mitigate current challenges within the caregiving role.
阿尔茨海默病及与阿尔茨海默病相关的痴呆症代表着复杂的神经病理学状况,给美国的个人、其家庭和社区带来了直接挑战。为了支持痴呆症患者,家庭或非正式照料者常常面临复杂的财务、心理和身体方面的挑战。一个广泛使用的解决方案,如整合的基于网络的援助或指导平台缺失,这加剧了照料方面的挑战。
为设计一个基于互联网的人工智能驱动的数字资源平台做准备,开展了一项定性访谈研究,以描述美国家庭照料者面临的挑战和需求。
通过与社区伙伴和研究伙伴合作,制定了一份英文的半结构化访谈主题指南。通过各种方式有目的地招募家庭照料者参与者,如口口相传、当地痴呆症社区服务提供者、数字招募邮件、传单和社交媒体。首先邀请感兴趣的个人完成资格筛选调查,然后联系符合条件的个人,安排于2022年1月1日至2022年5月31日通过Zoom(Zoom视频通信公司)进行基于网络的深入访谈。2022年5月进行了一项后续调查,以提供参与者的人口统计学、社会经济特征和照料信息的概述。采用框架方法进行主题分析,以识别和组织主题及研究结果。
在对150名符合条件的受访者进行预筛选后,20%(30/150)的个人完成了访谈和后续调查,从而能够深入了解痴呆症患者主要照料者面临的挑战、经历和期望。大多数参与者(20/30,67%)是痴呆症患者的主要照料者,93%(28/30)提供照料至少一年。大多数参与者年龄超过50岁(25/30,83%),女性(23/30,77%),白人(25/30,83%),非西班牙裔(27/30,90%),拥有学士或研究生学位(22/30,73%)。总体而言,所有参与者都承认在照料痴呆症患者方面存在挑战。主题分析得出了与功能照料需求以及财务和法律挑战相关的照料挑战。此外,参与者确定需要一个综合数字平台,在该平台上可以提供信息以促进教育、共享资源并提供社区支持,使家庭照料者能够提高照料质量并减轻照料者负担。
本研究强调了家庭照料者角色所带来的困难以及基于网络的支持性平台减轻当前照料角色挑战的期望和潜力。