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Software and hardware issues in data collection cannot be resolved.
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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Acute Cognitive Training Followed by Non-stimulating Rest Group | Experimental | Participants will be in this group for approximately 11-14 days |
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| Non-stimulating rest followed by acute cognitive training Group | Experimental | Participants will be in this group for approximately 11-14 days |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Acute Cognitive Training | Device | Participants will receive the intervention in person once within in the study for 30 minutes. During the intervention, participants will receive a cognitive training session consisting of an upper extremity, lower extremity, and whole-body reaction time task. The device (5 LED) will be placed in front of participants in all tasks, and participants will be asked to deactivate lights that illuminate for a period of 30 seconds with 30 seconds of rest. For the upper and lower extremity tasks, these will be repeated on both limbs. The purpose of the tasks are to pre-train reaction time in an isolated fashion, requiring participants to use either hands or feet to deactivate the lights, as well as incorporate whole-body movement in the third task along with a decision-making (color-matching) component. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Reaction Time | Will be measured in seconds (s) | Up to 5 minutes before and up to 5 minutes after intervention |
| Change in Percentage of Correct Responses in Cognitive-Motor Running T-test | Percentage of correct responses on cognitive-motor test | Up to 5 minutes before and up to 5 minutes after intervention |
| Change in Completion Time | Will be measured in seconds (s) | Up to 5 minutes before and up to 5 minutes after intervention |
| Change in Hop distance | Will be measured in meters (m) | Up to 10 minutes before and up to 10 minutes after intervention |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Zachary A Ripic, PhD | University of Miami | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Miami | Coral Gables | Florida | 33146 | United States |
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| ID | Term |
|---|---|
| D001265 | Athletic Injuries |
| ID | Term |
|---|---|
| D014947 | Wounds and Injuries |
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| Non-stimulating Rest | Other | Participants will receive the intervention in person once within the study for 30 minutes. During the intervention, participants will watch, while seated, a 30-minute segment of a nature documentary. The purpose of this intervention is to ensure no additional cognitive or movement training that would improve performance on the dual-task test occurs during the intended rest period. |
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