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CompletedNCT03975023Updated Jan 27, 2021

Investigating Event-Related Potentials and Eye-Tracking Measures in Hockey Players

An observational study in Healthy and Traumatic Brain Injury, sponsored by Frederick Carrick, PhD, FACCN. Completed at 1 site in United States. Open to participants aged 14 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-01-27.

Sponsored by Frederick Carrick, PhD, FACCN · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
52
Ages
14 Years to 25 Years
Sex
All
01

Study summary

Traumatic brain injury (TBI) is a health issue impacting athletes and no clinical treatment protocol, other than rest, is yet established. The efficacy of a treatment protocol relies on objective, physiological measures of brain function and ultimately a quantification of injury severity.

The present study aims to assess neurophysiological markers of auditory and visual measures of brain function using the NeuroCatch Platform and eye-tracking technology, respectively. The current gold standard of TBI evaluation, including cognitive and balance assessments, will also be captured.

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Conditions studied

  • Healthy
  • Traumatic Brain Injury
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In context

Brain Injuries

2,113 studies on the registry are indexed under Brain Injuries; 385 are open to participants now.

This study's enrollment of 52 is below the median of 100 across 690 observational studies indexed under Brain Injuries.

Browse Brain Injuries studies →

Lead sponsor

This is the only study on the registry with Frederick Carrick, PhD, FACCN as lead sponsor.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
14 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Up to 70 hockey players aged 14-25 years will be included in the study.

Inclusion criteria

  • Any sex, 14-25 years old inclusively
  • Attending the Creative Artists Agency LLC (CAA) hockey camp in July 2019
  • Able to understand the informed consent/assent form, study procedures and willing to participate in study

NeuroCatch Platform-Specific Inclusion Criteria

  • Able to remain seated and focused for 6 minutes
  • Normal hearing capabilities

Exclusion criteria

Exclusion Criteria:

  • Unable to provide informed consent

NeuroCatch Platform-Specific Exclusion Criteria

  • Clinically documented hearing issues (e.g. tinnitus, in-ear hearing problems or punctured ear drum)
  • In-ear hearing aid or cochlear implant, hearing device
  • Implanted pacemaker or defibrillator
  • Metal or plastic implants in skull
  • Exposed to an investigational drug or device 30 days prior to start in this study, or concurrent or planned use of investigational drug or device during hockey camp (July 7th - 13th 2019)
  • Not proficient in English
  • Previous exposure to the NeuroCatch™ Platform audio sequences in the last 6 months
  • History of seizures
  • Allergy to rubbing alcohol or EEG gel
  • Unhealthy scalp (apparent open wounds and/or bruised or weakened skin)
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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
52 participants (actual)
Patient registry
No

Groups and cohorts

  • hockey players

    During each study visit, the participants will undergo the following procedures: * NeuroCatch Platform (NCP) assessment (only if participant meets NCP-specific criteria) * RightEye's eye-tracking battery * Highmark Interactive's EQ application * Cambridge Brain Science's neuropsychological tests

    Device: NeuroCatch Platform (NCP)

Interventions

  • DeviceNeuroCatch Platform (NCP)

    The NCP plays a proprietary 6-minute auditory stimulus sequence of tones and words that elicit involuntary evoked responses in the brain. Tone stimuli elicit N100 and P300 responses, and spoken word pairs elicit N400 responses. The NCP proprietary software identifies the latency and amplitude (timing and size) of three selected ERPs. Latency and amplitude values are reported as empirical (measured) values.

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What researchers measure

Primary outcomes

  1. ERP response size

    amplitude in microvolts

    Time frame: 1 week

  2. ERP response timing

    latency in milliseconds

    Time frame: 1 week

  3. Eye-tracking: target accuracy

    distance in millimeters for each eye

    Time frame: 1 week

  4. Eye-tracking: speed

    degrees per second

    Time frame: 1 week

Secondary outcomes

  1. Cognitive tests

    Cognitive assessments will be captured using Cambridge Brain Sciences battery of neuropsychological tests (composite score) and Highmark Interactive's EQ app

    Time frame: 1 year

  2. Balance

    Balance measured in seconds as captured by Highmark Interactive's EQ app

    Time frame: 1 week

Other outcomes

  1. Trends between outcome measures and demographics will be explored

    Demographics include age, concussion history, and handedness

    Time frame: 1 year

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Study locations

1 site
  • The Carrick Institute
    Cape Cañaveral, Florida 32920, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 27, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03975023
Lead sponsor
Frederick Carrick, PhD, FACCN
Collaborators
HealthTech Connex Inc.
Responsible party
Frederick Carrick, PhD, FACCN (Prof Frederick R Carrick, Carrick Institute for Graduate Studies) — Sponsor-investigator
First posted
Jun 5, 2019
Start date
Jul 7, 2019
Primary completion
Jul 11, 2019
Completion
Apr 16, 2020
Last update
Jan 27, 2021

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2021. You cannot join it, but the record below documents what was studied.

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