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临床试验/NCT00692328
NCT00692328已完成不适用

Expectation and Response to Levodopa & Acupuncture in Parkinson's Disease

Oregon Health and Science University2 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2005年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
63
试验地点
2
主要终点
Fatigue rate and muscle response evoked by transcranial muscle stimulation (TMS)

研究概览

简要总结

To investigate how levodopa and acupuncture affect fatigue and muscle function in people who suffer from Parkinson's disease. Subjects may choose to participate in levodopa or acupuncture part, or both. Study procedures include an exercise protocol, transcranial magnetic stimulation (a non-invasive type of brain stimulation that cause small muscle twitch), a blood draw, and personality surveys.

详细描述

Subjects will answer surveys, have their blood drawn, undergo TMS and perform an exercise. The TMS/exercise task will measure fatigue and muscle response. The surveys will describe personality and measure fatigue. The CTRC will do genotype studies on the blood to look for genetic differences. Each subject is eligible to receive both study treatment types (levodopa and acupuncture). Depending upon the study treatment type they choose, each subject will be randomly assigned to one of six possible subject groups:

Ia. Full expectancy; levodopa: Subjects will be told that they are taking levodopa.

Ib. Half expectancy; levodopa: Subjects will be told that they have 50% chance of receiving levodopa or placebo.

Ic. No expectancy; levodopa: Subjects will be told that they are receiving placebo levodopa.

IIa. Full expectancy; acupuncture: Subjects will be told that they are receiving real acupuncture.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Clinical diagnosis of Parkinson's disease
  • Able to withdraw Parkinson's disease medication for 12 hours prior to a study visit
  • Must be currently using levodopa to qualify for the levodopa part of the study

排除标准

  • History of seizures
  • Presence of any metal in the body, including DBS stimulators, pacemakers, metal plates or pins
  • Severe cognitive deficits or psychosis
  • Evidence of any clinically unstable disease, such as cancer, HIV/AIDS; unstable heart condition or other conditions that might require hospitalization
  • Evidence of another neurological disease, such as multiple sclerosis, amyotrophic lateral sclerosis, or Huntington's disease

结局指标

主要结局

Fatigue rate and muscle response evoked by transcranial muscle stimulation (TMS)

时间窗: Before and immediately after the intervention

次要结局

未报告次要终点

研究者

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

Barry S. Oken

MD

Oregon Health and Science University

研究点 (2)

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