FITLIGHT Reliability and Acute Training Effects

Not Applicable

Recruiting

• Conditions: Athletic Injuries

• Registration Number: NCT06748417
• Lead Sponsor: University of Miami

Brief Summary

The purpose of this study is to assess the reliability of outcomes collected using a speed and cognitive light training system. This study will also be used to understand the effects of brain training on athletic performance using the FITLIGHT System.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2024-12-19
• Study First Submitted QC: 2024-12-19
• Study First Posted: 2024-12-27
• Study Start: 2025-02-18
• Status Verified: 2025-04
• Last Update Submitted: 2025-04-21
• Last Update Posted: 2025-04-22
• Primary Completion: 2025-10-01
• Study Completion: 2025-12-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Healthy as determined by a Physical Activity Readiness Questionnaire
• BMI under 30

Exclusion Criteria

• Color-blindness
• Fractures within the past year
• Musculoskeletal injury limiting sports activity within the past 6 months
• Anterior cruciate ligament (ACL) injuries within the past 5 years
• Medical conditions that do not have physician clearance to participate in exercise
• History of concussion
• Diagnosed cognitive impairments
• Untreated attention deficit/hyperactivity disorder (ADHD) or attention deficit disorder (ADD)
• Prisoners
• Pregnant women
• Smokers

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Primary Outcome Measures

Name	Time	Method
Change in Reaction Time	Up to 5 minutes before and up to 5 minutes after intervention	Will be measured in seconds (s)
Change in Percentage of Correct Responses in Cognitive-Motor Running T-test	Up to 5 minutes before and up to 5 minutes after intervention	Percentage of correct responses on cognitive-motor test
Change in Completion Time	Up to 5 minutes before and up to 5 minutes after intervention	Will be measured in seconds (s)
Change in Hop distance	Up to 10 minutes before and up to 10 minutes after intervention	Will be measured in meters (m)

Trial Locations

Locations (1)

University of Miami; 🇺🇸 Coral Gables, Florida, United States