Digital Detection of Dementia (D Cubed) Studies: D2
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 5,325
- 试验地点
- 2
- 主要终点
- 12-Month Cumulative Incidence of ADRD Diagnoses
研究概览
简要总结
The specific aim of the pragmatic trial is to evaluate the practical utility and effect of the PDM, the QDRS, and the combined approach (PDM + QDRS) in improving the annual rate of new documented ADRD diagnosis in primary care practices.
详细描述
Alzheimer's disease and related dementias (ADRD) negatively impact millions of Americans with an annual societal cost of more than $200 million.1 Currently, half of Americans living with ADRD never receive a diagnosis.2-7 For those who do, the diagnosis often occurs two to five years after the onset of symptoms.6-9 As stated by the National Institute on Aging (NIA) (RFA-AG-20-051) "The inability to diagnose and treat cognitive impairment results in prolonged and expensive medical care" and "early detection could help persons with dementia and their care partners plan for the future". Furthermore, if the development of disease modifying therapeutics for ADRD is successful, this may require the use of such therapeutics at a very early stage of ADRD.1 However, the current approaches of using cognitive tests or biomarkers for early detection of ADRD are not scalable due to their low acceptance, their invasive nature, their cost, or their lack of accessibility in rural or underserved areas. Thus, the NIA called out for the development of low cost, effective, and scalable approaches for early detection of ADRD (RFA-AG-20-051).
In response to the RFA-AG-20-051 call for the "validation, and translation of screening and assessment tools for measuring cognitive decline a pragmatic cluster-randomized controlled comparative effectiveness (NIH Stage IV) trial will be executed in Eskenazi Health in central Indiana and one additional replicated pragmatic trial among patients from diverse rural, suburban and urban primary care practices in south Florida. The pragmatic trial will incorporate the Passive Digital Marker (PDM) and the Quick Dementia Rating Scale (QDRS) within the Medicare paid Annual Wellness Visit (AWV) for a cohort of patients from practices across the two independent sites, with practices randomized in each pragmatic trial to one of the 3 arms (AWV alone, the AWV with PDM and the PDM and the QDRS).
Quick Dementia Rating Scale (QDRS)- is a validated patient reported outcome (PRO) tool.
Passive Digital Marker (PDM) - is a Machine Learning (ML) algorithm which can predict ADRD one year and three years prior to its onset by using routine care electronic health record (EHR) data. The algorithm was trained using structured and unstructured data from three EHR datasets: diagnosis (Dx), prescriptions (Rx), and medical notes (Nx). Individual algorithms derived from each of the three datasets were developed and compared to a combined one that included all three datasets.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Screening
- 盲法
- Double (Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 65 Years 至 —(Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •65 years or older
- •At least one visit to primary care practice within the past year
- •Ability to provide informed consent
- •Ability to communicate in English or Spanish
- •Available EHR data from at least the past three years
排除标准
- •Prior ADRD or mild cognitive impairment diagnosis as determined by ICD-10 code
- •Evidence of any history of prescription for a cholinesterase inhibitors or memantine.
- •Has serious mental illness such as bipolar or schizophrenia as determined by ICD-10 code
- •Permanent resident of a nursing facility
结局指标
主要结局
12-Month Cumulative Incidence of ADRD Diagnoses
时间窗: 12 months after index visit
Any new ADRD case identified (documented in the EHR) within 12 months of the Annual Wellness Visit (index visit).
次要结局
- 12-Month Cumulative Incidence of ADRD Services(12 months after index visit)
研究者
MALAZ BOUSTANI
Professor of Aging Research
Indiana University
