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A Machine Learning Approach for Inferring Alcohol Intoxication Levels From Gait Data (Alcogait)

2020年4月5日 更新者:Michael Stein, MD、Butler Hospital
This study aims to develop a phone app to assess gait differences at different levels of alcohol intoxication.

研究概览

地位

完全的

条件

详细说明

250 adult volunteers who will each participate in a single laboratory-based visit. At the orientation, each participant will provide informed consent, be weighed, and undergo a medical history to confirm eligibility. A urine drug quick-screen will be given. Female participants will take a urine pregnancy test. Baseline questionnaires will be administered. After giving participants the phone on which the AlcoGait 2.0 app is installed, baseline assessment of gait will be performed with the participant walking a distance of 50 yards ten times.

Drinking will then commence. The total amount will be consumed over 30 minutes. Participants will have their BrAC assessed multiple times during and after drinking has commenced and finished. At BrAC levels of .02, .04, .06 and .08 g%, will perform the gait task. After the last gait task, participant data will be transmitted to a secure server. Participants will receive a meal, and will be escorted to a sitting area with a DVR and videos, and allowed to use their own electronic devices. Their BrAC will be periodically tested until it reaches .02 g% or below, then a taxi will be called to take them home.

研究类型

介入性

注册 (实际的)

141

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Rhode Island
      • Providence、Rhode Island、美国、02906
        • Butler Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

21年 至 75年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • ages 21-65
  • drinking at least 5 drinks per occasion for men (4 for women) during a single drinking episode at least once in the last month to ensure, for safety reasons, that people are accustomed to consuming alcohol in amounts comparable to what we will administer
  • willingness to drink beer (since only beer will be provided in the session to standardize drinks more easily).

Exclusion Criteria:

  • past 6 months or current treatment for alcohol or drug abuse by self-report (for ethical reasons)
  • Score > 5 on (the short version of the Michigan Alcohol Screening Test [SMAST]48) given during the screening interview
  • positive family history of alcohol use disorder
  • weight ≥ 230 lbs (to prevent excessive volume of beverage)
  • current use of medications that are contraindicated for alcohol
  • a health condition that contraindicates alcohol (e.g. peptic ulcer disease)
  • a health condition that affects ability to walk
  • if female, pregnant or nursing
  • use of recreational drugs (e.g., marijuana, opioids, stimulants, benzodiazepines) within the last week (self-report plus urine screening cup)
  • persons who report alcohol-induced flushing, an untoward reaction that is often accompanied by headache, nausea and other symptoms

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
其他:All Participants
All participants complete the same study procedures, which involve drinking alcohol to a .08 blood alcohol level and walking short distances while their blood alcohol level is increasing to .08 and decreasing down to .00.
all participants will participate in the same protocol involving drinking alcohol to a .08 g% blood alcohol level

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Phone App
大体时间:data from each participant will be collected during a one-visit study session
a phone app to compare gait changes with blood alcohol levels will be developed based on participant's gait during alcohol use
data from each participant will be collected during a one-visit study session

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2017年12月12日

初级完成 (实际的)

2019年7月31日

研究完成 (实际的)

2019年7月31日

研究注册日期

首次提交

2017年7月26日

首先提交符合 QC 标准的

2017年8月8日

首次发布 (实际的)

2017年8月11日

研究记录更新

最后更新发布 (实际的)

2020年4月7日

上次提交的符合 QC 标准的更新

2020年4月5日

最后验证

2020年4月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

All Participants的临床试验

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