Assessing Eye Tracking Features Following Sports-Related Concussion
NCT ID: NCT02103803
Last Updated: 2015-11-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
11 participants
OBSERVATIONAL
2014-02-28
2015-11-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Reverse King-Devick Test and History of Multiple Concussions
NCT04560400
Eyetracking and Neurovision Rehabilitation of Oculomotor Dysfunction in Mild Traumatic Brain Injury
NCT03319966
Effects of Soccer Heading on Ocular-motor Function and Blood Biomarker
NCT03488381
Eye Movement Recordings in the Diagnosis of Traumatic Brain Injury
NCT00875589
Correlation Between Changes in Measures of the Visual System and Changes in Concussion-associated Symptoms
NCT03259178
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The main objectives include:
1. Describing the oculometric deficits present in subjects with acute sports-related concussion.
2. Analyzing and quantifying the oculometric changes that occur during subject recovery.
3. Identifying possible oculometric features as potential biomarkers that may lead to reliable, rapid method for recognizing acute concussion.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Have documented diagnosis of sports-related concussion within two weeks of the event.
* Currently demonstrating post-concussion symptoms.
Exclusion Criteria
8 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Lee Family Foundation
UNKNOWN
Mayo Clinic
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Jamie M. Bogle, Au.D., Ph.D.
Senior Associate Consultant
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Gaurav Pradhan, PhD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Jan Stepanek, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Jamie Bogle, AuD, PhD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Mayo Clinic in Arizona
Scottsdale, Arizona, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
13-009632
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.