Brookdale Department of Geriatrics and Palliative Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
James J. Peters Veterans Affairs Medical Center, Geriatric Research Education and Clinical Center (GRECC), Bronx, New York, USA.
J Am Geriatr Soc. 2024 Aug;72(8):2544-2551. doi: 10.1111/jgs.18966. Epub 2024 May 22.
Recruitment and retention are common challenges in clinical trials, particularly with older adults and their caregivers who often benefit from palliative care but have significant strain from caregiving. In recent years, there has been an expansion in home-based palliative care programs, especially for patients with dementia. Because these programs often rely on physicians or advanced practice nurses, they are quite costly and may be difficult to staff due to workforce shortages.
We created a novel program of home-based palliative care for patients with advanced dementia and their families, which centers around a community health worker, a social worker, and a nurse. We report on challenges our trial encountered and corresponding solutions.
We enrolled 30 patients and their 30 caregivers in our pilot trial of home-based palliative care. We found two significant barriers to enrollment: (1) the electronic health record was insufficient to determine the severity of patients' dementia; and (2) rates of follow-up survey completion were low, with completion rates at 6 months between 14 and 44%. We created an iterative training process to determine dementia severity from electronic health records and applied person-centered approaches to improve survey completion.
Electronic health records are not set up to include discrete fields for dementia severity, which makes enrollment of older adults with dementia in a clinical trial challenging. The strain of caring for a loved one with advanced dementia may also make participation in health-services research difficult for patients and their families. Novel approaches have the potential to counteract these challenges, improve recruitment and retention, and ultimately improve care for people with dementia and their caregivers.
招募和保留参与者是临床试验中常见的挑战,尤其是对于那些经常受益于姑息治疗但因照顾而承受巨大压力的老年患者及其照顾者。近年来,家庭姑息治疗项目有所增加,特别是针对痴呆症患者。由于这些项目通常依赖医生或高级执业护士,因此成本很高,并且由于劳动力短缺,可能难以配备人员。
我们为患有晚期痴呆症的患者及其家庭创建了一种新的家庭姑息治疗计划,该计划以社区卫生工作者、社会工作者和护士为中心。我们报告了试验中遇到的挑战和相应的解决方案。
我们在家庭姑息治疗的试点试验中招募了 30 名患者及其 30 名照顾者。我们发现了两个导致入组困难的主要障碍:(1)电子健康记录不足以确定患者痴呆症的严重程度;(2)随访调查完成率较低,6 个月时的完成率在 14%至 44%之间。我们创建了一个迭代培训过程,以从电子健康记录中确定痴呆症的严重程度,并采用以患者为中心的方法来提高调查完成率。
电子健康记录没有设置用于痴呆症严重程度的离散字段,这使得招募患有痴呆症的老年患者参加临床试验具有挑战性。照顾患有晚期痴呆症的亲人的压力也可能使患者及其家属难以参与健康服务研究。新方法有可能克服这些挑战,提高招募和保留率,并最终改善痴呆症患者及其照顾者的护理。