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Comparing Driving Performance Among Trained and Untrained Drivers Using a Driving Simulator

Children's Hospital of Philadelphia (CHOP) logo

Children's Hospital of Philadelphia (CHOP)

Status

Completed

Conditions

Accident Prevention
Accidents, Traffic
Prevention Harmful Effects

Treatments

Behavioral: Risk Anticipation -Perception Training

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01619202
12-009288
K99NR013548 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to examine differences in driving performance on a simulated driving assessment between novice teen drivers who receive the Risk Anticipation-Perception Training (RAPT) program and novice teen drivers who do not receive the training program.

Full description

Motor vehicle crashes remain the number one cause of death among teens in the United States. Teen drivers (ages 16 to 19) are four times more likely to be involved in fatal crashes than adult drivers (ages 25 to 69). Driving simulators are a safer alternative to on-road assessments that are often affordable and can provide experimental control for research. Though driving simulators have advantages for evaluating driving performance in teens, there are gaps in the literature on the validity of a multidimensional outcome of driving performance in a simulator. To further examine the validity of a multidimensional measure of driving performance in a simulator, we compare simulated driving performance among teens who are trained hazard anticipation-perception training and those who are not.

Enrollment

50 patients

Sex

All

Ages

16 to 18 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Holds a valid driver's license for less than or equal to 180 days
  • 16 - 18 years of age

Exclusion criteria

  • Self-reports claustrophobia, migraine headaches, and/or motion sickness
  • Females who are pregnant
  • Previously participated in another CHOP driving simulator study
  • Non-English Speaking

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

Risk Anticipation-Perception Training
Experimental group
Description:
Complete the Risk Anticipation-Perception Training (RAPT) program
Treatment:
Behavioral: Risk Anticipation -Perception Training
No training program
No Intervention group
Description:
Does not complete the Risk Anticipation-Perception Training (RAPT) program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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