Skip to main content
Clinical Trials/NCT06748417
NCT06748417TerminatedNot Applicable

Reliability of the FITLIGHT System and Acute Effects of Cognitive Training on Dual-task Performance in Hopping and Cutting Assessments

University of Miami2 sites in 1 country8 target enrollmentStarted: February 18, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
8
Locations
2
Primary Endpoint
Change in Reaction Time

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Device Feasibility
Masking
None

Eligibility Criteria

Ages
18 Years to 25 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Outcomes

Primary Outcomes

Change in Reaction Time

Time Frame: 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

Time Frame: Up to 5 minutes before and up to 5 minutes after intervention

Percentage of correct responses on cognitive-motor test

Change in Completion Time

Time Frame: Up to 5 minutes before and up to 5 minutes after intervention

Will be measured in seconds (s)

Change in Hop distance

Time Frame: Up to 10 minutes before and up to 10 minutes after intervention

Will be measured in meters (m)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Zachary Ripic

Principal Investigator

University of Miami

Study Sites (2)

Loading locations...

Similar Trials