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Validation of driving-related psychometric tests to predict performance on a standard on-the-road test after prolonged wakefulness.

Validation of driving-related psychometric tests to predict performance on a standard on-the-road test after prolonged wakefulness. - Predicting impaired driving

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON37179
Enrollment
24
Registered
2012-12-11
Start date
2013-01-01
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

n.v.t. Het betreft gezonde vrijwilligers die alleen langer wakker gehouden zullen worden n.v.t.

Interventions

The intervention is prolonged wakefulness (24 hrs.)

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Healthy Age between 23 and 45 (inclusive) BMI between 19 and 29 (inclusive) In posession of a valid driving license for at least 4 years Driving experience of at least 5000 km/year on average Normal sleeping pattern

Exclusion criteria

Exclusion criteria: Abnormal sleeping pattern (sleeping disorder; extreme morning or evening type; night shifts) Smoking Excessive alcohol use (more than 21 glasses of alcohol per week) Excessive caffeine use (more than 5 cups of coffee per day) Use of drugs

Design outcomes

Primary

MeasureTime frame
The primary study parameters are: - the reaction time on the Psychomotor Vigilance Test - the Standard Deviation of Lateral Position (SDLP) on the standard Highway Driving Test.

Secondary

MeasureTime frame
De secundary study parameters are accuracy and speed on the other computer tests that will be performed by the subjects. Like: - Critical Tracking Test - Divided Attention Test - Concept Shifting Test - Useful Field Of View - Digit Symbol Substitution Test - Attentional Networks Test - Determination Test - Reaction Time Test

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)