Longitudinal Assessment of Post-concussion Driving in Young Adults (LAPDYA)
Project Number5R01NS131273-02
Contact PI/Project LeaderSCHMIDT, JULIANNE D
Awardee OrganizationUNIVERSITY OF GEORGIA
Description
Abstract Text
PROJECT SUMMARY/ABSTRACT
Upwards of 3.8 million concussions occur annually in the United States. Only 44% of concussed individuals
reduce their driving at any point following injury despite emergent concerns over post-concussion driving
safety, documented driving impairment, and reports of feeling unsafe driving after a concussion. Most
concussed individuals who reduce their driving only do so for 24-48 hours following the injury. Driving is a
highly complicated activity that requires visual, motor, and cognitive skills, which are commonly impaired after
concussion. Concussed individuals cross the centerline more frequently within 48 hours of injury and present
with poorer vehicle control throughout the full symptom recovery. Yet, the time course of post-concussion
driving impairment has not been characterized. There is a critical need to 1) determine when concussed
individuals should return to driving and 2) identify the key concussion assessment predictors of readiness to
return to driving. In the absence of formal recommendations, impaired concussed drivers are at risk to
themselves and others on the road. The first specific aim is to compare simulated driving between concussed
individuals and non-concussed yoked matched controls across five longitudinal timepoints (pre-injury baseline,
day 2, day 4, asymptomatic, and unrestricted medical clearance) and daily naturalistic driving from day 2 to
day 9. Driving recommendations must be appropriate and necessitated by concussion impairments, since
excessively strict recommendations wrongfully strip concussed patients of their independence and may
dissuade individuals from seeking medical care. The second specific aim is to identify widely used
concussion assessment outcomes that predict simulated driving performance among concussed individuals
throughout concussion recovery. To address these aims, 100 concussed and 100 yoked matched control
young adult college athletes will complete a simulated driving assessment and a robust concussion
assessment battery at pre-injury baseline, day 2, day 4, asymptomatic, and unrestricted medical clearance.
Naturalistic driving (measured with in-car global positioning systems) will be captured from day 2 to day 9 (7
days total). This study will determine the acute and subacute time course of post-concussion driving
impairment and determine key predictors of post-concussion driving performance. Results from this innovative
approach will have a broad and positive impact that will improve the safety of both concussed individuals and
the general population, guide the practices of health professionals, inform the future work of researchers, and
substantiate the work of policy-makers by providing evidence-based recommendations for managing post-
concussion driving.
Public Health Relevance Statement
PROJECT NARRATIVE
The proposed research is relevant to public health because it will (1) improve the safety of concussed
individuals and the general population that use roadways, (2) guide the practices of health professionals, and
(3) substantiate the work of policy-makers by providing strong evidence-based recommendations for managing
post-concussion driving. This translational study is relevant to the mission of both the NIH and NINDS because
it provides fundamental knowledge about how brain injury burdens concussed drivers, while also identifying
which widely used clinical outcomes are associated with post-concussion driving impairment.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AccidentsAcuteAddressAgeAutomobile DrivingBrain ConcussionBrain InjuriesCaringClinicalClinical assessmentsCommunitiesDataEquilibriumExhibitsFeelingFreedomFrequenciesFrightFunctional impairmentFundingFutureGaitGeneral PopulationGlobal Positioning SystemGoalsHealth ProfessionalHourImpairmentIncidenceIndividualInjuryKnowledgeLateralMeasuresMedicalMemoryMissionMotorMotor SkillsNational Institute of Neurological Disorders and StrokeNeurocognitionNeurocognitiveOutcomeOutcome AssessmentParticipantPatientsPolicy MakerPositioning AttributePublic HealthPublishingReadinessRecommendationRecoveryReportingResearchResearch PersonnelRiskRisk FactorsSafetySamplingSpeedSymptomsTimeUnited StatesUnited States National Institutes of HealthVehicle crashVisualWorkclinical predictorsclinically relevantcognitive skillcollegecomparison controldriving performancedriving safetyevidence baseevidence based guidelinesexecutive functionimpaired driving performanceimprovedinjury burdeninnovationmedical attentionmild traumatic brain injuryoutcome predictionprocessing speedpsychosocialtranslational studyunsafe drivingyoung adult
National Institute of Neurological Disorders and Stroke
CFDA Code
853
DUNS Number
004315578
UEI
NMJHD63STRC5
Project Start Date
01-September-2023
Project End Date
31-May-2028
Budget Start Date
01-June-2024
Budget End Date
31-May-2025
Project Funding Information for 2024
Total Funding
$356,522
Direct Costs
$263,528
Indirect Costs
$92,994
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Neurological Disorders and Stroke
$356,522
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01NS131273-02
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5R01NS131273-02
Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 5R01NS131273-02
Clinical Studies
No Clinical Studies information available for 5R01NS131273-02
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History
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Similar Projects
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