CClinicalTrials.gg
CompletedNCT04051138Updated Jan 27, 2021

The Effect of VOXX/eSmartr High Performance Technology on Sports Vision Ability

An interventional study of Voxx socks and sleeves in Vision, Binocular and Sports Medicine, sponsored by ChampionsEdge, LLC. Completed at 1 site in United States. Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-01-27.

Sponsored by ChampionsEdge, LLC · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
All
01

Study summary

This study is designed to compare the effect of Voxx/eSmartr technology on common measures of sports vision performance including (Hand-Eye Coordination/Reaction time, visual concentration and basic visual functions of size detection and contrast sensitivity). The study will be a randomized, prospective, double-blind design in order to determine the effect of this technology on a subject's sports vision ability.

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Conditions studied

  • Vision, Binocular
  • Sports Medicine
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In context

Lead sponsor

This is the only study on the registry with ChampionsEdge, LLC as lead sponsor.

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

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Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Female or Male age 18-45 years of age
  • Exercises at least once a week by self-report
  • Physically able to complete the HEC/RT test (e.g. no shoulder or arm discomfort or limitation

Exclusion criteria

Exclusion Criteria.

  • Member of a vulnerable population
  • Visual or physical condition which precludes performing the physical or visual testing (e.g. strabismus, double vision, shoulder or arm pain or injury)
  • Previous training in hand-eye coordination/reaction time or visual concentration
  • History of double vision or strabismus
  • Insufficient vision to drive an automobile in NY State
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Single group
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
50 participants (actual)

Interventions

  • OtherVoxx socks and sleeves

    participants will be tested with a true device as well as with a placebo device

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What researchers measure

Primary outcomes

  1. CoreScore

    A measure of visual function scored on a linear scale fro +5 to -5, more positive scores are better

    Time frame: 1 day

Secondary outcomes

  1. Hand-Eye Coordination/Reaction Time

    A measure of how fast the subject reacts to a visual target with their hand, scored on milliseconds, faster the better

    Time frame: 1 day

  2. Neurotracker score

    A measure of how correctly the subject can track multiple objects, scored from 0 to 5 with higher score being better

    Time frame: 1 day

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Study locations

1 site
  • SportsVisionNYC
    New York, New York 10019, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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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
NCT04051138
Lead sponsor
ChampionsEdge, LLC
Responsible party
Sponsor
First posted
Aug 9, 2019
Start date
Aug 15, 2019
Primary completion
Oct 30, 2019
Completion
Oct 30, 2019
Last update
Jan 27, 2021

Study contacts

Daniel M Laby, MD
principal investigator · ChampionsEdge, LLC

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
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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