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临床试验/NCT00457769
NCT00457769Unknown1 期

Phase 1 Study of Aricept Plus a Behavioral Strategy to Improve Functional Tasks in Vascular Dementia

Kessler Foundation1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2007年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
发起方
入组人数
18
试验地点
1
主要终点
Primary: To examine whether taking Aricept results in improvement at remembering steps of functional tasks.

研究概览

简要总结

Medications for memory improvement are available but they may not actually improve the ability to do real world tasks. The purpose of this research study is to determine if a medicine used to treat memory problems donepezil(Aricept) enhances the ability to remember steps of functional tasks and the actual ability to perform tasks relevant to real-life independence. Aricept is an FDA approved medication for the treatment of Alzheimer's disease. Aricept is an investigational drug for the purposes of this study, and is not approved for this purpose.

详细描述

All participants will receive a behavioral intervention as part of the testing protocol: they will be asked to generate words to complete a phrase as they read written steps to perform functional tasks. Mood will be assessed using the Geriatric Depression Scale.(see page 8) Participants will be asked to estimate their memory, immediate attention mood, functional tasks (performing cooking and financial task) and "ability to take medications correctly" (pre-test or "offline" ratings, abstract judgments of their own ability not based directly on performance). They will perform self-assessments of their cognitive, functional abilities and mood using Likert scales. They will mark each of 5 vertical (23.5 cm) lines centered on white paper to indicate their ability. Each line will be labeled for each domain.

To estimate of naming ability, show the subject the Likert Scale (attached) for the naming domain. Then explain: "This scale is to measure how well you think your ability to name. Here is the top where you will mark if you think your performance is perfect, here is the bottom if you think you are terrible. You may be somewhere in between. (broadly indicated the whole middle area) mark where you think your performance would belong on this scale".

This standard protocol will be used by the examiner in this study to explain each domain with specific types of tasks, and give subjects practical hypothetical examples of good and poor performance.

Ability to take medication: Functional memory as applied to medication compliance will be assessed with the Hopkins Medication Schedule (HMS). This test has two part, HMS and pill box. The test will serve as a good evaluation of subject's functional memory, which we suspect it will be most strongly affected by Anosognosia.

The HMS: the participant was read (and read along with) a hypothetical scenario in which her physician gave her 1 prescription for an antibiotic and for aspirin to treat an infection along with directions for taking each. The participant was then asked to plan a schedule for taking these medications and water during the course of a day, following the instructions provided.

研究设计

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

入排标准

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

入选标准

  • I am 18 to100 yrs old.
  • I had one stroke 4 months to 5 yrs ago
  • I am not taking Aricept or other cholinesterase inhibitors (e.g. Exelon, Razadyne) or memantine (Namenda).

排除标准

  • I have history of dementia and or have been diagnosed with a memory disorder prior to my stroke.
  • I have been on anti-depressants or other cognitive enhancing drugs for less than 3 months and the dose is not stabilized yet.
  • I consume alcohol more than or equivalent of 4 ounces hard liquor weekly.
  • I am taking oral anticholinergic medications like Bethanechol, Bentyl or Detrol.
  • I am a woman of childbearing potential or I am pregnant or a nursing mother.
  • I have a history of chronic vomiting or diarrhea.
  • I am allergic to Aricept.

研究组 & 干预措施

Aricept- A

Experimental

Half of subjects are randomized to immediate treatment with donepezil 5mg orally daily following baseline testing, with retesting at 12 and 24 weeks.

干预措施: Donepezil and self-generated memory training (Drug)

Aricept- A

Experimental

Half of subjects are randomized to immediate treatment with donepezil 5mg orally daily following baseline testing, with retesting at 12 and 24 weeks.

干预措施: Donepezil and experimenter-administered memory training (Drug)

A2-12-week waiting period

Experimental

The remaining nine subjects are randomized to testing followed by a 12-week waiting period. After the 12 week wait, this group of subjects is retested and begins taking donepezil, 5 mg orally daily, with retesting at 24 weeks

干预措施: Donepezil and self-generated memory training (Drug)

A2-12-week waiting period

Experimental

The remaining nine subjects are randomized to testing followed by a 12-week waiting period. After the 12 week wait, this group of subjects is retested and begins taking donepezil, 5 mg orally daily, with retesting at 24 weeks

干预措施: Donepezil and experimenter-administered memory training (Drug)

结局指标

主要结局

Primary: To examine whether taking Aricept results in improvement at remembering steps of functional tasks.

时间窗: 12 weeks

次要结局

  • To examine whether taking Aricept and actually performing functional tasks improves memory over that provided by a self-generation strategy.(24 weeks)

研究者

发起方
Kessler Foundation
申办方类型
Other
责任方
Principal Investigator
主要研究者

A. M. Barrett, MD

Director, Stroke Rehabilitation Research

Kessler Foundation

研究点 (1)

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