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Clinical Trials/NCT07282405
NCT07282405Enrolling By InvitationNot Applicable

Validation of Alcohol Level Identification Using DRIVESC

University of Wisconsin, Madison1 site in 1 country22 target enrollmentStarted: November 11, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
22
Locations
1
Primary Endpoint
Proportion of Enrolled Participants who Complete all Scheduled Activities

Study Overview

Brief Summary

This pilot study will evaluate the feasibility and acceptability of using a commercially available DRIVESC fitness-to-drive measurement tool to detect alcohol-induced impairment in healthy adult participants. The investigators hypothesize that DRIVESC can detect measurable changes in driving-related cognitive and motor performance across blood alcohol concentrations up to the U.S. per se legal limit of 0.08% g/210L ethanol. The study will enroll healthy adults aged 18-64 years (including both dosed and zero-alcohol arms) participating in the Wisconsin Breath Alcohol Examiner Specialist course, with each participant completing two study visits over two days.

Detailed Description

A total of 18-22 participants will be enrolled in this single-site partial crossover pilot study. Under the auspices of the Wisconsin Basic Breath Examiner Specialist training, participants will be dosed with alcohol on the first, second, or neither day of the three-day training.

This study design includes 6 double-alcohol-negative participants who will complete two days of alcohol-negative study tasks. The investigators will consider enrolling 12 alcohol-positive participants a success but are aiming to enroll 16 alcohol-positive participants. Alcohol-positive participants will complete two days of study tasks where one day is alcohol-negative and the other day is alcohol-positive. The order of positive-negative and negative-positive will be balanced. This range allows for flexibility in this feasibility study as study activities are scheduled in coordination with and around Chemical Testing Section training activities to minimize disruption to their educational tasks.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Crossover
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to 64 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Participants will be included in this study if they are trainees, observers, or instructors in the Wisconsin Basic Breath Examiner Specialist training program
  • Meet the age requirements for their assigned study arm (18 years or older for non-drinking, 21 years or older for drinking), and
  • Are able to provide informed consent.

Exclusion Criteria

  • Participants will be excluded from this study if they are unable to provide informed consent
  • Do not meet the age requirements for their assigned study arm, or
  • Are determined to be not suitable for participation due to other reasons at the discretion of the study team.

Outcomes

Primary Outcomes

Proportion of Enrolled Participants who Complete all Scheduled Activities

Time Frame: through day 2

Data will be recorded as completed vs not completed measurements or timepoints for each participant session.

Secondary Outcomes

  • Within-Participant Change in DRIVESC Composite Score from Day 1 to Day 2: Non-Drinking Arm(through day 2)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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