NCT02125825已完成不适用
Kinesia-D Phase II In-Clinic Continuous Assessment Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 14
- 试验地点
- 2
- 主要终点
- Correlation between motion sensor features and clinician-rated dyskinesia severity
研究概览
简要总结
The objective is to assess a compact, portable, wireless movement disorder system with continuous monitoring capabilities to detect and quantify the severity of levodopa-induced dyskinesia in Parkinson's disease.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 21 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosis of idiopathic Parkinson's disease
- •Clinical history of levodopa-induced dyskinesia
- •21 Years of age or older
- •Stage 2 - 4 OFF-medication on the Hoehn and Yahr scale
排除标准
- •Dementia (determined by a neuropsychological assessment)
- •Severe tremor unaffected by levodopa
结局指标
主要结局
Correlation between motion sensor features and clinician-rated dyskinesia severity
时间窗: All data will be collected within a single session not to exceed 3 hours
Motor function (movement speed and magnitude measured with a motion sensor) will be collected for a period of 2 hours after taking normally prescribed dose of levodopa.
次要结局
未报告次要终点
研究者
研究点 (2)
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