NCT04859868已完成不适用
Non-pharmaceutical Motion Sickness Mitigation
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Mayo Clinic
- 入组人数
- 29
- 试验地点
- 2
- 主要终点
- Motion Perception
研究概览
简要总结
The purpose of this study is evaluate the effect of timing and magnitude on the administration of our nonpharmaceutical treatment to motion sickness, and to evaluate the effect of Galvanic Vestibular Stimulation (GVR) amplitude on functional fitness task performance.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 21 Years 至 55 Years(Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Must be able to consent to participate themselves.
- •Must be able to attend in-person sessions at the Mayo Aerospace Medicine and Vestibular Research Laboratory in Scottsdale, AZ.
- •No racial ethnic groups will be excluded.
- •Must be fluent speakers of English.
排除标准
- •History of vestibular disease, migraine, or significant balance disorder.
- •Traumatic brain injury.
- •Recent middle ear infection or recent motion sickness (within 72 hours).
- •History of severe motion sensitivity.
- •Women who are pregnant.
结局指标
主要结局
Motion Perception
时间窗: During the rotation of the chair, approximately 1 hr
Motion Perception verbal report using a visual analog scale (1-100) will be recorded during the rotation of the chair (1=feeling no motion perception; 100=feeling the maximum motion perception)
次要结局
- Motion Sickness Questionnaire(During the rotation of the chair, approximately 1 hr)
研究者
Gaurav N. Pradhan
Principal Investigator
Mayo Clinic
研究点 (2)
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