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Effects of tDCS on High Level and Recreational Athletes

Not Applicable
Completed
Conditions
Healthy
Athlete
Interventions
Device: tDCS
Registration Number
NCT03893604
Lead Sponsor
University of Liege
Brief Summary

Healthy recreational and high level athletes will undergo 2 randomized, cross-over counterbalanced sessions of anodal tDCS or sham tDCS.

The primary outcome is an isokinetic evaluation of their hamstrings' and quadriceps' endurance after each session

Detailed Description

Recruitment :

Healthy recreational and high level athletes will be recruited through social media and advertisements.

Each subject came twice to the Liege University Hospitals' isokinetic lab. Each session began with strapping the subjet into the isokinetic machine, making sure that all the settings were adapted to the subject. Then, each subject received either anodal tDCS, of sham tDCS. Neither the evaluator or the subject knew which they were receiving. Immediately following tDCS, there was a warmup consisting of stationary bike, and an isokinetic warmup. Then, subjects' endurance was using a maximal isokinetic tests, at 30 maximal concentric and eccentric contractions at a speed of 180°/s.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
60
Inclusion Criteria
  • For the "recreational" group at most 3 hours of sport a week
  • For the "athletic" group, at least 10 hours of sport a week
  • Right handed and footed
Exclusion Criteria
  • One on the TSST (in high and relatively high risk sections)
  • Previous neurological or orthopedic pathologies affecting limbs

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Sham tDCStDCSSubjects will receive 20 minutes of Sham anodal tDCS
Anodal tDCStDCSSubjects will receive 20min anodal tDCS
Primary Outcome Measures
NameTimeMethod
Peak StrengthImmediately after tDCS and sham

Peak strength (measured by the isokinetic machine) is measured after each of the 30 repetitions.

Peak strength of the 30 repetitions will be measured, and how strength decreases throughout the test will be analysed

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Liege Univeristy Hospital

🇧🇪

Liege, Belgium

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