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临床试验/NCT01672489
NCT01672489进行中(未招募)不适用

Objective Assessment of the Effects of Shift Work on Drowsiness and Driving Impairment in Hospital Staff

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2011年7月最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
19
试验地点
1
主要终点
Participants' fatigue and drowsiness level measured by an eye tracker device.

研究概览

简要总结

The purpose of this protocol is to assess the risk of drowsy driving amongst shift workers using objective measures of drowsiness and driving performance in an instrumented research vehicle.

详细描述

Specific Aim 1. To test the hypothesis that on road (track) driving performance will deteriorate (variation in lateral lane position and the rate of out of lane driving events) and the frequency of episodes of severe sleepiness will increase ("microsleeps" on EEG and Johns' Drowsiness Score >4) in shift workers following an extended work shift or night shift compared to a rested state, following day shifts.

Specific Aim 2. To test the hypothesis that ocular measures of alertness (percent of time with eyes closed, eye tracking and Johns' Drowsiness Score) are related to abnormal driving performance (driving out of the lane) and "microsleeps" during on road (track) driving.

Specific Aim 2a. To test the hypothesis that autonomic measures, ECG, respiration (measured with the Bioharness), skin conductance level and peripheral blood flow (measured with the Q sensor), are related to abnormal driving performance (driving out of the lane) and "microsleeps" during on road (track) driving

Specific Aim 3. To test the hypothesis that self-reported sleepiness is related to on road (track) driving performance and episodes of severe sleepiness following extended working shifts or night shifts.

研究设计

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

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participant must be a shift worker who undertakes extended duration shifts (16 hours or longer) or overnight shifts
  • Participant must be between the ages of 18-65y
  • Participant needs to have held a US driving license for two years previously or an International Driving license for two years with 6-months regular (>2/week) US driving experience
  • Participants who wear corrective eye wear (i.e., glasses) are ONLY eligible to participate if they have a valid prescription so we can fit the Optalert glasses with their prescription lenses
  • Resident physicians are only recruited if the combination of their time involvement in the study (i.e., any additional time beyond the time that it would ordinarily take them to commute home from work), together with their scheduled work hours, would fall within ACGME standards for duty hours for resident physicians.

排除标准

  • Exclusion criteria includes all parameters outside the inclusion criteria above.

结局指标

主要结局

Participants' fatigue and drowsiness level measured by an eye tracker device.

时间窗: Up to 3 hours per session for each participant.

An eye tracking device, owned by Liberty Mutual, is used to measure eye activity.

Participants' fatigue and drowsiness level while driving using Optalert.

时间窗: Up to 3 hours per session for each participant.

Optalert is a portable device, worn like sunglasses, designed to detect drowsiness, particularly when driving.

Driving performance measured by an instrumented vehicle.

时间窗: Up to 3 hours per session for each participant.

A dual control instrumented vehicle, owned by Liberty Mutual, has been used for each driving session with each subject. This vehicle is fitted with a lane tracking system, as well as the capability to instruct and record responses from the driver. Lane position is monitored and recorded continuously with lateral and rear facing cameras. Data is logged to on-board computers.

Participant's awareness of their fatigue level using a composite of survey data taken by each participant.

时间窗: Surveys are taken by the participant every 15 minutes during regular stops during each session.

Questionnaires include: Karolinska Sleepiness Scale, Likelihood of Falling Asleep Questionnaire, and the Sleepiness Symptoms Questionnaire.

Brain activity including "microsleeps" using electroencephalography (EEG).

时间窗: Up to 3 hours per session for each participant.

Continuous EEG recordings are made during each track driving session using a portable Vitaport 4 system (Temec ®).

Alertness level and level of fatigue measured by a composite of variables from a Zephyr Bioharness device worn by each participant.

时间窗: Up to 3 hours per session for each participant.

The Zephyr Bioharness uses smart fabric sensors (non-adhesive) to measure electrocardiography (ecg), respiratory wave form, chest skin temperature, posture and activity (3-axis accelerometer).

Alertness level and level of fatigue from a composite of variables measured by an Affectiva Q-Sensor worn by each participant.

时间窗: Up to 3 hours per session for each participant.

Additional autonomic nervous systems measures are obtained from a wrist-worn sensor (Affectiva Q-Sensor).

次要结局

  • Sleep and wake times using an Actiwatch device.(Up to 7 weeks per subject worn continuously during enrollment in the study.)
  • Participants' view of their health and well-being using a composite of surveys administered during subject enrollment.(Up to 2 hours per subject during the start of their participation in the study.)
  • Sleep and wake times using a 'sleep and work' diary completed by each subject.(Up to 7 weeks per participant completed daily.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Charles A. Czeisler, PhD, MD

Charles A. Czeisler PH.D., M.D.

Brigham and Women's Hospital

研究点 (1)

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