Clinical Trials Directory

Trials / Completed

CompletedNCT02881788

Minnesota Healthy Brain Initiative

Status
Completed
Phase
Study type
Observational
Enrollment
690 (actual)
Sponsor
Hennepin Healthcare Research Institute · Academic / Other
Sex
All
Age
4 Years – 100 Years
Healthy volunteers
Accepted

Summary

Minnesota Healthy Brain Initiative will be an ongoing project that aims to increase awareness regarding brain health and its maintenance as well as increasing awareness of the impact of alcohol on brain function. In the immediate future, we hope to obtain data from a non-injured normative, diverse population represented by the state fair patrons.

Detailed description

We hypothesize that a non-invasive 30-minute test, requiring a subject to complete questionnaires and watch images on a TV screen, will yield information relevant to both diagnosis and prognosis of neurological state. To clarify, these tests will not produce information that would involve a diagnostic finding for the participants. We will measure eye movements under a range of visual conditions, including saccades, fixations, smooth pursuit, scan paths and optico-kinetic nystagmus After receiving proper introduction and signing the proper consent forms, the subject will receive instructions to carry out cognitive assessments and answer verbal questionnaires. The subject will also undergo eye tracking. In order to validate the data collected by our eye-trackers, we may ask the subject to complete a non-invasive vision assessment and a breathalyzer assessment. Due to the nature of the breathalyzer assessment, we have decided not to administer the breathalyzer assessment to subjects who are under the age of 21 and/or pregnant. We also refuse to disclose the results of the breathalyzer assessment to the subject since the data will be collected only for research purposes. Subjects' eye movements will be tracked binocularly at a fixed distance from a computer monitor over a brief time period. The visual stimuli will be video clips appropriate for a general or pediatric audience. If at any point the subject becomes uncomfortable, the procedure will be aborted and can be resumed at a later time.

Conditions

Timeline

Start date
2016-08-01
Primary completion
2018-06-01
Completion
2018-06-01
First posted
2016-08-29
Last updated
2020-10-19

Source: ClinicalTrials.gov record NCT02881788. Inclusion in this directory is not an endorsement.