FITLIGHT Reliability and Acute Training Effects

University of Miami

Status: Terminated

Conditions: Athletic Injuries

Treatments: Device: Acute Cognitive Training; Other: Non-stimulating Rest

Study type: Interventional

Funder types: Other

Identifiers

NCT06748417

20241122

Details and patient eligibility

About

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.

Enrollment: 8 patients

Sex: All

Ages: 18 to 25 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Device Feasibility

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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8 participants in 2 patient groups

Acute Cognitive Training Followed by Non-stimulating Rest Group

Experimental group

Description:

Participants will be in this group for approximately 11-14 days

Treatment:

Other: Non-stimulating Rest

Device: Acute Cognitive Training

Non-stimulating rest followed by acute cognitive training Group

Experimental group

Description:

Participants will be in this group for approximately 11-14 days

Treatment:

Other: Non-stimulating Rest

Device: Acute Cognitive Training