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The purpose of this study is to develop and validate eye-tracking measures that can be used to evaluate neurocognitive dysfunction among individuals with traumatic brain injury (TBI).
This study will evaluate a novel method of neurocognitive assessment using computerized eye tracking. This method involves looking at targets on a computer screen while an eye-tracking system records eye movements and changes in pupil diameter in response to the presentation of the targets.
Performance on the eye tracking measures will be evaluated to identify potential effects of neural injury on cognitive performance. Data from individuals with and without a history of brain injury will be used to standardize the eye tracking measure.
Participants will also complete a short interview and several self report measures, including information about demographic characteristics, medical history, and psychological symptoms, along with a series of neuropsychological/cognitive measures that are already well established. Performance on eye tracking measures will then be compared to performance on these conventional cognitive tests to allow comparison of the different measures.
All participants will complete one visit to the laboratory at USUHS in Bethesda, MD. This visit will take approximately 2.5 hours. Participants without a history of TBI may be asked to return for a 30 minute follow-up session in order to measure the reliability of the eye tracking system. Participants with a history of TBI will complete a 10 minute telephone follow-up 6 and 12 months after their visit.
Compensation is available for civilians who are not employed by the Federal government.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| TBI Group | Adults (civilian or military) with a history of one or more brain injuries / concussions. | ||
| Control Group | Healthy adults (civilian or military) with no history of brain injury. |
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| Measure | Description | Time Frame |
|---|---|---|
| Performance on the eye tracking measures | Baseline |
| Measure | Description | Time Frame |
|---|---|---|
| Psychological symptoms | Baseline | |
| Performance on the neurocognitive assessment battery | Baseline | |
| Post-concussive symptoms |
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Inclusion Criteria (Control Group):
Exclusion Criteria (Control Group)
Inclusion Criteria (TBI Group):
Exclusion Criteria (TBI Group)
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The population to be studied will include civilians and military personnel with and without a history of traumatic brain injury / concussion.
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| Name | Affiliation | Role |
|---|---|---|
| Mark Ettenhofer, Ph.D | Uniformed Services University of the Health Sciences | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| USUHS | Bethesda | Maryland | 20814 | United States |
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| ID | Term |
|---|---|
| D000070642 | Brain Injuries, Traumatic |
| D038223 | Post-Concussion Syndrome |
| D001924 | Brain Concussion |
| D001930 | Brain Injuries |
| ID | Term |
|---|---|
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D006259 | Craniocerebral Trauma |
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| Baseline (and telephone follow-up, for TBI group) |
| D020196 | Trauma, Nervous System |
| D014947 | Wounds and Injuries |
| D016489 | Head Injuries, Closed |
| D014949 | Wounds, Nonpenetrating |