NCT07105462

Brief Summary

This randomized controlled trial is designed to investigate whether a novel visual training system can improve eye coordination, reaction time, and hitting accuracy in competitive badminton players. The training utilizes a device called the Automatic Dual Rotational Risley Prisms (ADRRPs), which presents alternating base-in and base-out prism demands to stimulate vergence eye movements. This type of training aims to enhance the eyes' ability to converge and diverge quickly and accurately-a function that is important for visual clarity and motor performance during fast-paced sports. A total of 26 collegiate badminton athletes aged 18 to 25 years will be recruited from two universities in Taiwan. Participants will be randomly assigned to one of two groups: a visual training group using the active ADRRPs system, and a control group using a sham version of the same device containing plano lenses (with no prism effect). Training will be delivered twice per week for four weeks, with each session lasting 15 minutes. During each session, participants will view a video while the device applies alternating prism stimulation based on each individual's pre-measured fusional vergence capacity. Outcome measures will be assessed at baseline and after the four-week training period. These include vergence facility (cycles per minute), accommodative facility (flipper test), near point of convergence, and positive fusional vergence at near. Reaction time will be measured using a light-based agility task with BlazePod sensors, and hitting performance will be evaluated using a shuttlecock launcher that delivers randomized targets to various court zones. All participants will be monitored for any adverse events, and any symptoms such as diplopia, dizziness, or discomfort will be documented. Data will be analyzed as described in the Statistical Analysis Plan.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
26

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 24, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 30, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

July 16, 2025

Completed
21 days until next milestone

First Posted

Study publicly available on registry

August 6, 2025

Completed
Last Updated

August 6, 2025

Status Verified

July 1, 2025

Enrollment Period

2 months

First QC Date

July 16, 2025

Last Update Submit

July 29, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Reaction Time Measured by BlazePod Test

    * Time in seconds required to complete 10 light-response trials using BlazePod; lower values indicate better performance. * Unit of Measure: seconds

    Baseline and Week 4 (post-intervention)

Secondary Outcomes (5)

  • Vergence Facility in Cycles per Minute (cpm)

    Baseline and Week 4

  • Accommodative Facility in Cycles per Minute (cpm)

    Baseline and Week 4

  • Near Point of Convergence Distance

    Baseline and Week 4

  • Positive Fusional Vergence Break and Recovery Points

    Baseline and Week 4

  • Number of Successful Shuttlecock Hits

    Baseline and Week 4

Study Arms (2)

Arm 1: Vergence Training with ADRRPs

EXPERIMENTAL

Participants assigned to this arm will receive vergence training using Automatic Dual Rotational Risley Prisms (ADRRPs), a computerized visual device designed to induce alternating base-out and base-in prism stimulation. The prisms rotate automatically to simulate dynamic convergence and divergence demands, cycling between 0 to 30 prism diopters base-out over 5 seconds and 30 base-out to 10 base-in over 3 seconds. Each participant will undergo 8 training sessions over 4 weeks (twice weekly), with each session lasting 15 minutes. During training, participants view standardized video targets positioned at a 40 cm working distance while instructed to maintain clear and single binocular vision. The intervention aims to engage and strengthen vergence eye movements critical for visual performance in dynamic sports environments.

Device: Arm 1 - Experimental Group Intervention Name: ADRRPs Vergence Training Intervention Description: Participants wore an Automatic Dual Rotational Risley Prism (ADRRPs) headset to perform vergence eye

Arm 2: Sham Training with Plano Lenses

SHAM COMPARATOR

Participants assigned to this arm will undergo sham vergence training using the same Automatic Dual Rotational Risley Prisms (ADRRPs) headset, but fitted with non-refractive plano lenses and with no prism rotation. The training schedule and environment are identical to the intervention arm: 8 sessions over 4 weeks (twice weekly), with each session lasting 15 minutes. Visual targets are presented at a 40 cm viewing distance using the same video stimuli. This sham training condition is designed to control for potential placebo effects and to isolate the specific influence of dynamic prism-induced vergence stimulation used in the experimental arm.

Device: 1. Experimental Group Intervention Name: ADRRPs-Based Vergence Training; 2. Control Group Intervention Name: Sham Training with Plano Lenses.

Interventions

ADRRPs Vergence Training Intervention Description: Participants wore an ADRRPs headset that applied alternating base-in and base-out prism power to stimulate vergence eye movements. Prism levels were customized based on each participant's fusional vergence. Training was performed twice weekly for 15 minutes over four weeks while viewing a near video target. Sham Visual Training with Plano Lenses Intervention Description: Participants wore an identical ADRRPs headset fitted with plano lenses that produced no prism effect. The procedure and schedule matched the experimental group but provided no vergence stimulation, serving as a sham control.

Arm 1: Vergence Training with ADRRPs

ADRRPs-Based Vergence Training This intervention used the Automatic Dual Rotational Risley Prisms (ADRRPs) system to deliver alternating base-in and base-out prism stimulation for vergence training. Prism levels were customized based on each participant's fusional vergence. Training was conducted twice per week for four weeks, 15 minutes per session, while participants viewed a near video target. This protocol provides automated and symmetric vergence demand, distinguishing it from conventional near-point or static prism exercises. Sham Training with Plano Lenses Participants used the same ADRRPs headset as the experimental group but with plano lenses that produced no prism effect. The training schedule and visual tasks matched the experimental condition, but no vergence stimulus was applied. This design enabled participant masking while providing no active optical stimulation, serving as a sham comparator distinct from both active training and no-treatment controls.

Arm 2: Sham Training with Plano Lenses

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Aged between 18 and 30 years
  • Minimum of 2 years of consistent badminton training
  • Best-corrected visual acuity of 20/25 or better in both eyes (distance and near)
  • No history of ocular pathology
  • Willingness to comply with all study procedures and follow-up

You may not qualify if:

  • Presence of constant strabismus or binocular vision anomaly
  • History of ocular trauma, strabismus surgery, or refractive surgery
  • Neurological or systemic conditions affecting vision
  • Ongoing medication that may influence ocular motor function

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Central Taiwan University of Science and Technology

Taichung, 402, Taiwan

Location

Study Officials

  • Hsuan-Yu Huang, Ph.D.

    College of Health Sciences, Central Taiwan University of Science and Technology

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 16, 2025

First Posted

August 6, 2025

Study Start

March 24, 2025

Primary Completion

May 30, 2025

Study Completion

May 30, 2025

Last Updated

August 6, 2025

Record last verified: 2025-07

Locations