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临床试验/NCT07126938
NCT07126938已完成不适用

An Observational Study to Facilitate the Development of an Alcohol Impairment Detection Device in Healthy Adult Alcohol Users

Gaize1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年3月21日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
80
试验地点
1
主要终点
Alcohol-Associated Ocular Impairments

研究概览

简要总结

This study evaluates the effectiveness of the Gaize virtual reality headset as a non-invasive tool for detecting alcohol-related impairment through ophthalmic and neurological indicators. A total of 80 participants, evenly divided into an experimental (alcohol-consuming) and control (non-alcohol consuming) group, underwent baseline and post-consumption ocular assessments using the device. These assessments included: Lack of Smooth Pursuit, Horizontal Gaze Nystagmus at Maximum Deviation, Horizontal Gaze Nystagmus with Onset Prior to 45-Degrees, Vertical Gaze Nystagmus, Lack of Convergence, and Pupillary Rebound Dilation. The Gaize headset measured gaze vector and pupil size at 90 hertz per eye.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
21 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Adults aged between 21 and 45, having given written informed consent to participate in the research trial and certifying that they do not intend to drive post discharge. We will consider extending the observation period based on individual participants' alcohol consumption.
  • Having used alcohol at least one time prior.
  • Having experienced impairment too severe to allow for safe operation of a vehicle or work from alcohol use.
  • Planning to drink alcohol during their time at the study location.
  • Without any history of severe reactions or allergy to alcohol.
  • Having access to legal alcohol.
  • Normal or corrected to normal vision using either glasses or contact lenses, or surgery.

排除标准

  • Enrolled in, or participated in another clinical trial within 30 days before the study
  • Having a prosthetic eye, blindness, or vision not corrected to normal.
  • Severe reactions or allergy to Alcohol. Participants with a history of severe adverse reactions to alcohol (e.g., allergies, intolerances, or medical conditions worsened by alcohol) are excluded.
  • Certain Medical Conditions: Participants with medical conditions or medications that could significantly affect cognitive and motor functions are excluded. A detailed list of such conditions and medications will be provided to potential participants during the screening process.
  • Pregnancy: Pregnant individuals will be excluded from the study due to the potential risks associated with alcohol consumption during pregnancy.
  • History of Severe Motion Sickness: Participants with a history of severe motion sickness in virtual reality environments may be excluded, as they may not tolerate the virtual reality headset well.
  • Individuals who have driven a vehicle (car, truck, bicycle, etc.) to the study location will not be eligible for participation.

研究组 & 干预措施

experimental

Consumes alcohol

干预措施: Alcoholic beverage (Drug)

结局指标

主要结局

Alcohol-Associated Ocular Impairments

时间窗: 1 hour after alcohol consumption

Number of participants and measurement of Lack of Smooth Pursuit, Horizontal Gaze Nystagmus at Maximum Deviation, Horizontal Gaze Nystagmus with Onset Prior to 45-Degrees, and Vertical Gaze Nystagmus were evaluated before and after alcohol consumption.

次要结局

  • Non-Alcohol Associated Ocular Impairments(1 hour after Alcohol consumption)

研究者

发起方
Gaize
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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