跳至主要内容
临床试验/NCT06191952
NCT06191952招募中不适用

Davos Alzheimer's Collaborative Healthcare System Preparedness to Increase Cognitive Assessment Rates for Older Adults

Ludwig-Maximilians - University of Munich2 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2023年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
500
试验地点
2
主要终点
Proportion of participating individuals screening positive for SCD

研究概览

简要总结

In this study the investigators explore a pragmatic strategy to increase cognitive screening rates in the community. The investigators will compare the monetary value of different combinations of SCD questionnaires, digital cognitive tests, and blood Alzheimer's Disease (AD) biomarkers to identify the best approach for primary care settings.

详细描述

The investigators aim to perform a cluster-randomized study, exploring the effectiveness, efficiency, and acceptability of a pragmatic strategy to increase cognitive screening rates in the community. Participants will be older adults attending social and cultural centers in the greater Munich area. The investigators will compare the monetary value of different combinations of SCD questionnaires, digital cognitive tests, and blood AD biomarkers to identify the best approach for primary care settings. As secondary aims, qualitative interviews will be conducted with general practitioners (GPs) and their patients to explore the acceptability of the proposed new screening strategy; furthermore, the diagnostic utility of an artificial intelligence-based automated analysis of speech will be assessed. The initiative will not only generate novel insights into the optimal approach for large-scale cognitive screening in the general population, but also contribute to an urgently required cultural change in Germany, resulting in a sustainable solution for effective and efficient early recognition and prevention of dementia.

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
None

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • age 65 years or older

排除标准

  • younger than 65 years

结局指标

主要结局

Proportion of participating individuals screening positive for SCD

时间窗: Baseline

The primary endpoint of this protocol is to assess the proportion of participating individuals aged 65 years or older screening positive for SCD during the intervention period who are referred to specialist evaluation, by study arm (intent to treat)

次要结局

  • Correlation with speech analysis and other diagnostic tests(Baseline)
  • Qualitative interviews(Baseline)
  • Proportion of individuals with early-stage AD diagnosis(Baseline)
  • average time to diagnosis of AD(Baseline)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Robert Perneczky

Principal Investigator

Ludwig-Maximilians - University of Munich

研究点 (2)

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