Stroboscopic Vision Training in Softball

Effect of Stroboscopic Vision Training in a Softball Season: A Randomized Controlled Trial Pilot Study

Enhanced sports performance, in our current world, is being pushed at the professional level and down to school-age children as well. Money is being spent on lessons and equipment to enhance performance. One new method to enhance performance is stroboscopic vision goggles. The glasses lenses flicker removing visual information for a brief moment. The claim is that they train connections between the eyes, brain, and body. We want to see if this product truly does enhance visual performance during a softball season for high school girls.

Study Overview

Status

Active, not recruiting

Detailed Description

In today's sports world, every strategy to perform at the highest level is needed. Current literature is demonstrating enhanced sports performance using stroboscopic vision training.1,2,5 The objective of this randomized controlled trial is to measure the effect of a stroboscopic visual training in a high school softball season in comparison to controls. Athletes in the control group will go through normal practice drills for hitting and fielding. The stroboscopic training (experimental group) will use the strobe glasses during hitting and fielding drills two times a week in practice. The brand of strobe glasses is Senaptec Strobe. Athletes in both the experimental and control groups will have their vision assessed at the beginning of the season and end by The West Texas Vision Center. Measurements for vision will include developmental eye movement, vergence ranges, Randot stereopsis test, accommodative ranges, acuity, and stereo scores. On-field performance measurements will be collected for batting statistics including on-base percentage, batting average, slugging percentage, and hard-hit ball percentage in both the experimental and control groups. The current year batting statistics will be compared with the prior year statistics if enough at-bats occurred. In addition, to the vision and on-field hitting performance proprioception balance using the Balance Error Scoring System (BESS) will be measured at the beginning of the season and end for both groups. Our data will provide quantified information for coaches, athletes, and health care providers concerning the benefits of the strobe glasses warrant buying to enhance sports performance. Additionally, we wish to determine whether visual-motor and proprioception balance changes occur after the training.

Study Type

Interventional

Enrollment (Estimated)

34

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Lubbock, Texas, United States, 79430
        • Texas Tech University Health Sciences Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years to 18 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 1) Age 14-18 years 2) females; 3) high school softball

Exclusion Criteria:

  • 1) Prior use of stroboscopic vision training; 2) History of seizures; 3) History of vestibular impairments

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Stroboscopic Training Group
Treatment group, which will receive stroboscopic training during hitting and fielding drills. The glasses look like sunglasses but have liquid crystal technology that causes a flicker from clear to opaque. The glasses flickering will be controlled on the side of the glasses by the researcher. When the athlete can complete a skill proficiently by catching or hitting during training the level of flickering will be increased to challenge the visual system more.
The glasses use liquid crystal technology that causes a flicker from clear to opaque to enhance vision.
Active Comparator: Standard softball drills
Control group, which will perform normal hitting and fielding drills without stroboscopic training
Control group, which will perform normal hitting and fielding drills without stroboscopic training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vergence ranges
Time Frame: 8 weeks
Vergence ranges measured how many prism diopters the subject can turn their eyes in (base out) and how far they can relax them out (base in). This score is also a good measure of how much peripheral fusion a person has.
8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Developmental eye movement
Time Frame: 8 weeks
Developmental eye movement will measure how fast the subject can track numbers vertically and horizontally.
8 weeks
Randot stereopsis test
Time Frame: 8 weeks
Randot stereopsis test will measures how many ARC seconds of stereo the subject has. This test measures the subject's magno and parvocellular stereo tracking their peripheral or central fusion.
8 weeks
Accommodative ranges
Time Frame: 8 weeks
Accommodative ranges will measure how many times the subject can clear an image looking through a plus and minus accommodation flipper in thirty seconds.
8 weeks
Acuity
Time Frame: 8 weeks
Acuity will measure the clarity of vision at a distance of twenty feet.
8 weeks
Stereo Scores
Time Frame: 8 weeks
Stereo Scores will measure how quickly the athlete recognizes depth perception
8 weeks
Batting statistics
Time Frame: 8 weeks
Batting statistics including on-base percentage, batting average, slugging percentage, hard-hit ball percentage will be provided by the coach at the end of the season for the current year and prior year. Subjects will need a minimum of 20 at-bats in a season for collection of these statistics.
8 weeks
Balance Error Scoring System (BESS)
Time Frame: 8 weeks
Balance Error Scoring System (BESS) measures the total number of postural errors committed in a 30-second trial standing on flat surface and foam pad. It provides a measure of balance and proprioceptive ability.
8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2021

Primary Completion (Estimated)

October 29, 2024

Study Completion (Estimated)

December 29, 2024

Study Registration Dates

First Submitted

March 12, 2020

First Submitted That Met QC Criteria

March 12, 2020

First Posted (Actual)

March 16, 2020

Study Record Updates

Last Update Posted (Estimated)

February 13, 2024

Last Update Submitted That Met QC Criteria

February 9, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • L20-095

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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