NCT02907723已完成不适用
Assessment of a Wrist Device Recording Sleep Parameters, Before and After Deep Brain Stimulation for Parkinson's Disease
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 5
- 主要终点
- mean sleep duration per night
研究概览
简要总结
This pilot study aims to assess a new device designed for an objective measure of sleep parameters. The purpose of the device is to assess, in a more simple and precise way, the impact of deep brain stimulation on patient's sleep.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 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
- 否
入选标准
- •patient > 18 years old
- •with Parkinson disease
- •scheduled for implantation of electrodes for deep brain stimulation
排除标准
- •pregnant or breast feeding patient
- •refusal to participate in the study
- •patient under legal protection
- •no health insurance coverage
研究组 & 干预措施
Continuous Sleep Recording
Experimental
Continuous Sleep Recording in Patients
干预措施: Sleep Recording (Device)
结局指标
主要结局
mean sleep duration per night
时间窗: 15 days
mean sleep onset latency
时间窗: 15 days
mean number of awakenings per night
时间窗: 15 days
次要结局
未报告次要终点
研究者
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