跳至主要内容
临床试验/NCT03081546
NCT03081546已完成不适用

Cross-Cultural Use of Performance-Based Functional Assessment in Alzheimer's Disease

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2017年5月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
41
试验地点
1
主要终点
University of California San Diego (UCSD) Performance-Based Skills Assessment (UPSA)

研究概览

简要总结

This study plans to assess the effectiveness of performance-based functional assessments (PBFAs) and cognitive assessments in diagnosing Alzheimer's disease in Hispanic/Latino populations. The information from this study will be analyzed with data from the Rocky Mountain Alzheimer's Disease Center Bio-AD study (NCT02612376).

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
55 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Persons with age-related MCI or AD according to clinical diagnosis, consistent with National Institute on Aging-Alzheimer's Association (NIA-AA) diagnostic criteria
  • Community-dwelling controls
  • Age > 55 years
  • Have been enrolled and completed at least one visit in the Bio-AD study and consent to access their data (the Rocky Mountain Alzheimer's Disease Center Bio-AD study (clinicaltrials.gov identifier: NCT02612376))
  • Have capacity to provide consent; capacity will be assessed at the time of consent
  • Ability to complete baseline assessments
  • Has informant (study partner) available to complete functional interviews/survey measures

排除标准

  • Presence of concomitant medical, neurological, or psychiatric illness or condition that in the opinion of the investigators would confound interpretation of study results. These include:
  • Korsakoff encephalopathy;
  • active substance abuse;
  • hepatitis C;
  • opportunistic brain infection;
  • brain tumor;
  • active neoplastic disease (skin tumors other than melanoma are not exclusionary; participants with stable prostate cancer may be included at the discretion of the project director);
  • multiple sclerosis;
  • history of clinically significant stroke;
  • current evidence or history in the past 2 years of
  • focal brain lesion,
  • head injury with loss of consciousness in the past year, or
  • DSM-5 criteria for any major psychiatric disorder, including
  • uncontrolled major depression,
  • bipolar disorder,
  • alcohol or substance abuse;
  • deafness or
  • any other disability which may prevent the participant from participating or cooperating in the protocol.
  • Prisoners
  • Any contraindication for MRI

结局指标

主要结局

University of California San Diego (UCSD) Performance-Based Skills Assessment (UPSA)

时间窗: 30 minutes

Measure independent functioning in everyday life for controls and individuals with MCI

Medication Management Ability Assessment

时间窗: 15 minutes

Measure independent management of medications in controls and individuals with MCI

Lawton iADL (instrumental activities of daily living) scale

时间窗: 5 minutes

Measure ability to perform instrumental activities of daily living in controls and individuals with MCI

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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