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This study will assess the effects of exercise and non-concussive bodily contact on eye-tracking scores collected by the EYE-SYNC eye-tracking device.
Full description
The investigators propose to prospectively study a cohort of 18-25-year-old athletes. Athletes will be tested with the EYE-SYNC eye-tracking device prior to the start of an athletic practice or competition (pre-test) and then after the conclusion of the practice/competition (post-test). The investigators hope to understand if eye-tracking scores are effected by exercise and non-concussive bodily contact commonly incurred during athletic play.
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Inclusion and exclusion criteria
Inclusion criteria
Exclusion criteria
Note: Under Cohort 1, Athletes that have conditions listed below will not be excluded from the study. They will be enrolled and their subject data will be analyzed separately from subjects who do not endorse any significant medical hx under neurological, eye-sight, or psychiatric categories.
Clinical diagnosis of a neurological condition including the following: Stroke, Multiple Sclerosis, Epilepsy, Brain Tumor/Cancer, Nystagmus and/or other major neurological condition.
Clinical diagnosis of any of the following eye-sight abnormalities: Uncorrected Amblyopia, Uncorrected Myopia, Uncorrected Presbyopia, Uncorrected Farsightedness, or Uncorrected Astigmatism.
Psychiatric history with any of the following:
Clinical diagnosis of a psychotic disorder, bipolar disorder - lifetime
Clinical diagnosis of ADHD or ADD - Lifetime
Clinical diagnosis of major depressive disorder - within last year
Clinical diagnosis of substance abuse disorder - within last year
Clinical diagnosis of major anxiety disorder - within last year
MEDICATION
Requires use of a psychotropic medication.
Primary purpose
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Interventional model
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155 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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