Control Study of Nautilus BrainPulse for the Detection of Concussion

Jan Medical, Inc.22 enrolled

Overview

To use the Nautilus BrainPulse to compare and contrast the signal patterns from this cohort's signal patterns with those of concussed high school athletes.

This study is a non-blinded study in high school athletes who will be presumed to no be suffering from a concussion. Healthy controls will be recruited from high school sports that are not associated with physical contact, which could generate concussions. The primary objective of this study is to improve Jan Medical's signal analysis. Jan Medical will perform analysis.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Brain Concussion

Interventions

Nautilus BrainPulseDEVICE

A noninvasive device to detect concussion utilizing headset and sensors

Eligibility

Sex: ALLMin age: 14 YearsMax age: 19 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Male and female between 14 and 19 years of age * Participating in non-contact sport at the Freshman, JV, and varsity level in a Bay Area High School * Able to provide signed informed consent or have a legally authorized representative willing to provide informed consent on the subject's behalf Exclusion Criteria: * History, if any, of concussion or stroke * History, if any, of alcohol or drug abuse * History, if any, of mental disorder or cerebrovascular disorder * Pregnant women * Failure to comply with recording schedule * Not suitable for participation in the study in the opinion of the PI * Have suffered a concussion during the study * Plays a contact sport (ex- football, lacrosse, basketball, soccer, ice hockey, cross-country) * Related to a Jan Medical employee

Locations (1)

Jan Medical, Inc.

Mountain View, California, United States

Outcomes

Primary Outcomes

To collect non-blinded Nautilus BrainPulseTM recordings from high school athletes who do not participate in a contact sport

BrainPulse recordings collected in this study will be used as an age-matched control cohort for comparison with already collected concussion data that is under development for identifying a concussion algorithm. The device recordings will be visually compared for similarities and differences using data mining practices looking for features that are consistent between the concussion subjects and healthy normals.

Time frame: 4 months

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.