Cognitive Training Psychomotor Performance
Conditions
Interventions
This is a two-arm randomized clinical trial, an open-label study, meaning it is not blinded, in which 24 individuals will participate (12 participants in the intervention group and 12 participants in
s timing.
Sponsors
Universidade do Vale do Rio dos Sinos
Universidade do Vale do Rio dos Sinos
Eligibility
Sex/Gender
Male
Age
14 Years to 18 Years
Inclusion criteria
Inclusion criteria: Male volleyball athletes; aged between 14 and 18 years; who have been regularly practicing the sport for at least six months; with a minimum frequency of two training sessions per week
Exclusion criteria
Exclusion criteria: Neurological conditions that may compromise cognitive processing or reaction time, for example, a recent history of concussion or traumatic brain injury; individuals with peripheral neurological lesions or dysfunctions such as neuropathies and peripheral nerve injury, which may alter sensorimotor representations and influence visuomotor responses; participants with acute or chronic lesions that limit the execution of tests such as joint instability, limiting pain, ligamentous injuries of the knee and ankle with functional restriction; regular use of medications that may affect attention or modify the response time to visual stimuli, such as anticonvulsants, opioid analgesics, antiepileptics, benzodiazepines, antidepressants, hypnotics, and antihistamines.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| A reduction in reaction time to stimuli is expected in the intervention group | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected | — |
Countries
BR
Contacts
Public ContactFabia Krumholz
Universidade do Vale do Rio dos Sinos
Outcome results
None listed