The RETINA Project: Reliable Eye Tracking in Neurocognitive Assessment of Traumatic Brain Injury



Status:Terminated
Conditions:Hospital, Neurology
Therapuetic Areas:Neurology, Other
Healthy:No
Age Range:18 - Any
Updated:12/19/2018
Start Date:October 2010
End Date:October 2017

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Eye Tracking Indicators of Neurocognitive Status After Traumatic Brain Injury

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.

Inclusion Criteria (Control Group):

- 18 years of age or older

- No history of brain injury or concussion

- Fluency and literacy in English

- Can effectively communicate verbally

- Willing and able to provide written informed consent

- Obtains signed permission to participate from supervisor and/or brigade commander
(federal civilian employees and active duty military personnel only).

Exclusion Criteria (Control Group)

- Impaired or fluctuating level of consciousness / arousal

- Any medical condition that could impair cognitive abilities (e.g. muscular dystrophy,
multiple sclerosis, psychosis)

- History of any neurological conditions such as brain tumor, brain infection, seizure
or stroke

- Any visual impairment that is not corrected by glasses/contacts

- Motor impairment or amputation of one or both upper extremities

Inclusion Criteria (TBI Group):

- 18 years of age or older

- History of one or more brain injuries / concussion

- Fluency and literacy in English

- Can effectively communicate verbally

- Willing and able to provide written informed consent

- Obtains signed permission to participate from supervisor and/or brigade commander
(federal civilian employees and active duty military personnel only).

Exclusion Criteria (TBI Group)

- Impaired or fluctuating level of consciousness / arousal

- Any medical condition that could impair cognitive abilities (e.g. muscular dystrophy,
multiple sclerosis, psychosis), other than TBI

- History of any neurological conditions (such as brain tumor, brain infection, seizure
or stroke) that was NOT associated with or resulting from traumatic brain injury

- Any visual impairment that is not corrected by glasses/contacts

- Motor impairment or amputation of one or both upper extremities
We found this trial at
1
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Bethesda, Maryland 20814
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Bethesda, MD
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