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Healthy ParticipantsNCT03572985

Development of Assessment Method for Driving Ability Using Driving Simulator in Healthy Volunteers #3

A study testing Road-tracking test, Car-following test and Harsh-braking test in people with Healthy Participants, run by Taisho Pharmaceutical Co., Ltd. at 1 site in Japan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to collect alcohol calibration data for the driving simulator. Read more about this study

Who is it for?
Ages 21 to 64 years, men onlyHealthy volunteers can take part
Conditions the study is for
Healthy Participants
What is being tested?
Road-tracking test, Car-following test and Harsh-braking test
Could I receive a placebo?
No, everyone receives an active treatment
How many people
25 participants
Where
1 siteJapan
Study dates
27 Jun 2018to 31 Jan 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 to 64 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Body mass index (BMI) ≥18.5 and <25.0 kg/m^2 at screening inspection
  • No visual impairment (enable to correct the vision with eyeglasses or contact lens)
  • Receive a prior explanation on the study, able to accept its content, and capable to provide voluntary written consent for participation in this study

Who cannot join

  • History of drug and food allergy
  • Alcohol dependence, drug dependence or abnormal drunken (including past history)
  • Inappropriate for enrollment in this study was judged by principal investigator or subinvestigator

Trial locations and contacts

1 site in 1 country.

Japan1 site
  • Taisho Pharmaceutical Co., Ltd selected site

    Fukuoka

Other trials in Japan

About this study

Official title: Development of Assessment Method for Driving Ability Using Driving Simulator in Healthy Volunteers #3: Alcohol Calibration

The purpose of this study is to collect alcohol calibration data for the driving simulator.

Being tested
Road-tracking test, Car-following test, Harsh-braking test

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Road-tracking testOther

    Driving with simulator program for SDLP measurement

  • Car-following testOther

    Driving with simulator program for DCV measurement

  • Harsh-braking testOther

    Driving with simulator program for BRT measurement

Study groups in NCT03572985
Study groupRoleWhat they receive
Blood alcohol concentration (BAC) level 0.025 %OtherDrink beverages containing alcohol calculated to have a blood alcohol concentration of 0.025%
Receives: Other: Road-tracking test; Other: Car-following test; Other: Harsh-braking test
BAC level 0.05 %OtherDrink beverages containing alcohol calculated to have a blood alcohol concentration of 0.05%
Receives: Other: Road-tracking test; Other: Car-following test; Other: Harsh-braking test
BAC level 0.09 %OtherDrink beverages containing alcohol calculated to have a blood alcohol concentration of 0.09%
Receives: Other: Road-tracking test; Other: Car-following test; Other: Harsh-braking test
BAC level 0 %OtherDrink beverages containing non alcohol
Receives: Other: Road-tracking test; Other: Car-following test; Other: Harsh-braking test

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Standard Deviation of Lateral Position (SDLP)

    Measured: 60 min

Secondary outcomes (2)
  1. Distance Coefficient of Variation (DCV)

    Measured: 5 min

  2. Brake Reaction Time (BRT)

    Measured: 5 min

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Jun 2018
  2. Study start27 Jun 2018
  3. Primary completion31 Jan 2019
  4. Study completion31 Jan 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Crossover
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
25 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03572985
Sponsor's protocol ID
DS-204-03
Other IDs
JapicCTI-184006
Status last verified
Nov 2019
First submitted
19 Jun 2018
Last updated
28 Feb 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Iwata M, Iwamoto K, Omura T, Ando M, Ozaki N. Protocol for the development and validation of a driving simulator for evaluating the influence of drugs on driving performance. Medicine (Baltimore). 2019 Feb;98(8):e14613. doi: 10.1097/MD.0000000000014613.

    PubMed 30813188

Questions about this trial

What is this clinical trial studying?

A study testing Road-tracking test, Car-following test and Harsh-braking test in people with Healthy Participants, run by Taisho Pharmaceutical Co., Ltd. at 1 site in Japan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Japan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Standard Deviation of Lateral Position (SDLP) (time frame: 60 min). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03572985, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Feb 2025; AzTrials last refreshed its copy on 27 Oct 2026.

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