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临床试验/NCT06928298
NCT06928298招募中不适用

Cognitive Screening Made Easy for PCPs - Administrative Supplement

University of Texas at Austin3 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年6月10日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
100
试验地点
3
主要终点
Cognitive Performance Score

研究概览

简要总结

This project will facilitate early detection of cognitive decline in older adults through development and implementation of an automated risk assessment and cognitive screening tool for use in primary care. By providing an automated tool developed specifically to address the needs of PCPs, it will be easier to screen for cognitive impairment, increasing the number of older adults who are screened and thus identified and treated.

详细描述

In the United States and around the world, people are living longer lives. As the population ages, so does the number of older adults who may experience declines in memory, attention, reasoning, or other thinking skills. Some of these changes in cognition can be treated and reversed if caught early. Others can be slowed down and hopefully one day prevented. Unfortunately, people with cognitive decline or very mild dementia often are not recognized until late in the disease course when treatments are less effective. As the first health care professional most people reach out to about medical concerns, primary care providers play a critical role in detecting cognitive decline early. While many primary care providers conduct cognitive screening at Medicare Annual Wellness Visits and when patients voice concerns, 9 out of 10 would like more information about who to screen, which assessment tool to use, and what to say if screening is positive. Deciding who to screen with a brief cognitive assessment tool is a key part of the process because not everyone needs to be screened, and primary care providers already face time pressures to address the obvious and immediate concerns of their patients. The long-term goal of this project is to develop a risk assessment and cognitive screening tool that requires minimal time and effort from primary care providers or their staff and is sensitive to cognitive decline in older adults from diverse educational and racial/ethnic backgrounds. The tool will be integrated into electronic health record systems to make it easy for primary care providers and patients to see results. The specific aims for the administrative supplement of the R33 phase of this project are to further test the effectiveness of the newly developed risk assessment and cognitive screening application in 100 Spanish speaking older adults receiving care in primary care clinics, to find out from primary care providers using the tool how much they liked it and if it was useful and easy to use, and to integrate findings into multiple electronic health record systems. Findings from this project will fill a gap in the existing toolkit of primary care providers and will make screening for cognitive decline quick, easy, effective and accessible in more than one language.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Screening
盲法
None

入排标准

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

入选标准

  • Inclusion Criteria:
  • Aged 60 years and older;
  • Ethnic/racial background consistent with NIH policy
  • Male or female
  • Fluent in Spanish.

排除标准

  • Confounding conditions that could impact ability to participate in the study (e.g., cognitive impairment sufficient to impact ability to follow instructions on the iPad, motor impairment that would prohibit independent use of RACS, poor visual acuity)
  • Prior diagnosis of dementia
  • Non-Spanish speaking.

研究组 & 干预措施

Intervention

Other

Risk assessment and cognitive screening app that includes questions answered by the participant and completion of a working memory task and two speech tasks

干预措施: RACS app (Behavioral)

结局指标

主要结局

Cognitive Performance Score

时间窗: baseline, 6 month, and 12 month visits

Combination of symbol matching and voice tasks, which generates a cognitive performance score ranging from 0 to 1 (high scores mean higher likelihood of cognitive impairment)

次要结局

  • Usability(baseline, 6 month, and 12 month visits)

研究者

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

Robin C. Hilsabeck

Professor

The University of Texas Health Science Center at San Antonio

研究点 (3)

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