此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Cognitive Impairment in Kidney Disease

2017年8月15日 更新者:VA Office of Research and Development

Functional and Cognitive Impairment in Advanced Kidney Disease

An increasing number of Veterans are anticipated to develop chronic kidney disease (CKD) and require hemodialysis (HD) treatments as the Veteran population ages. In 2003, approximately 290,000 US citizens were receiving HD and an estimated 19 million were affected by CKD. The annual growth rate is predicted to be 7% per year with 500,000 Americans receiving HD treatment by 2010. In 2005, approximately 2500 Veterans were receiving HD with growth expected to parallel that seen in the general population. Whereas Alzheimer's disease is the leading cause of dementia in the general population, growing evidence suggests that patients with advanced CKD experience cognitive deficits related to accelerated cerebrovascular disease. Patients with advanced CKD have been shown to have a high prevalence of sub-clinical cerebrovascular damage on imaging studies and a heavy burden of vascular risk factors such as diabetes, elevated cholesterol, and hypertension. Many of the cognitive deficits related to cerebrovascular disease may go unrecognized by routine measures of cognition. HD patients have increased number of hospitalizations, and several compliance issues ranging from congestive heart failure to dangerous electrolyte imbalances. Impaired cognition in this population is likely to have a significant impact on self-care and compliance with complex medical regimens. Currently, the severity and scope of cognitive impairment related to vascular disease is not well known in patients with advanced kidney disease. Additionally, the relationship between cognitive impairment and measures of self-care independence are not well known. Loss of independence and function secondary to impaired cognitive function is likely to be a significant problem for patients with advanced kidney disease. Early identification of functional impairment, particularly instrumental activities of daily living (IADL), will allow for rehabilitation intervention. Maintaining or improving functional independence through intensive rehabilitation could translate into better compliance and lower hospitalization rate among HD patients. Information obtained from this study is likely to heighten awareness of cognitive impairment and the functional consequences in Veterans with advanced kidney disease. Primary objectives are to determine:

  1. The range of cognitive deficits with emphasis on domains affected by vascular disease in patients with advanced CKD and those receiving hemodialysis.
  2. The associations between severity of cognitive impairment and severity of kidney disease.
  3. The prevalence of impaired IADLs and the level of health-related quality of life (HRQOL) in patients with advanced CKD and those requiring hemodialysis.
  4. The relationship or association of cognitive impairment with IADL and HRQOL.

Secondary objective is to determine:

1. The relationships among cerebral and carotid blood flow, carotid artery stiffness, and renal specific metabolic abnormalities with cognitive impairment.

研究概览

地位

完全的

研究类型

观察性的

注册 (实际的)

117

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • New York
      • The Bronx、New York、美国、10468
        • James J. Peters VA Medical Center, Bronx, NY

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 89年 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Veterans at the Bronx VA Renal Clinic, Hemodialysis Unit, and Primary Care Clinic

描述

Inclusion Criteria:

PreHD Subjects:

  • Male or female with an age of 18 years or older (no upper limit);
  • Patients with stage III-IV CKD attending the renal primary care clinic or renal consult clinic;
  • Fluent in English;
  • Outpatient or stable nursing home patient

HD Subjects:

  • Receiving HD for at least two weeks;
  • Male or female with an age of 18 years or older (no upper limit);
  • Fluent in English;
  • Outpatient or stable nursing home patient

Control Subjects:

  • Glomerular filtration rate of 60 cc/minute or greater;
  • Male or female with an age of 18y or older (no upper limit);
  • Fluent in English
  • Outpatient

Exclusion Criteria:

PreHD Subjects:

  • Acute illness;
  • Clinical history of stroke, dementia, or Parkinson's disease;
  • Hb <10;
  • Liver function tests 2x upper limit of normal;
  • Hemodialysis

HD Subjects:

  • Acute illness;
  • Clinical history of stroke, dementia, or Parkinson's disease;
  • Hb <10;
  • Liver function tests 2x upper limit of normal;
  • URR <65% (measure of dialysis adequacy: will use 3-month average from chart)

Control Subjects:

  • Acute illness;
  • Clinical history of stroke, dementia, or Parkinson's disease;
  • Hb <10;
  • Liver function tests 2x upper limit of normal;
  • Stage 3-4 CKD;
  • Hemodialysis

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
Control
No kidney disease
PreHD kidney disease
Kidney disease stage 4 or below
Hemodialysis
Kidney disease receiving hemodialysis

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Neuropsychological Assessments
大体时间:1 year
battery of neurocognitive tests
1 year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:James B Post, MD、James J. Peters Veterans Affairs Medical Center

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2006年12月1日

初级完成 (实际的)

2012年9月28日

研究完成 (实际的)

2017年7月20日

研究注册日期

首次提交

2009年5月18日

首先提交符合 QC 标准的

2009年5月19日

首次发布 (估计)

2009年5月20日

研究记录更新

最后更新发布 (实际的)

2017年8月18日

上次提交的符合 QC 标准的更新

2017年8月15日

最后验证

2017年8月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

在美国制造并从美国出口的产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

3
订阅