Effects of tDCS on High Level and Recreational Athletes
- Conditions
- HealthyAthlete
- 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
- 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
- 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
Group Intervention Description Sham tDCS tDCS Subjects will receive 20 minutes of Sham anodal tDCS Anodal tDCS tDCS Subjects will receive 20min anodal tDCS
- Primary Outcome Measures
Name Time Method Peak Strength Immediately 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
Name Time Method
Trial Locations
- Locations (1)
Liege Univeristy Hospital
🇧🇪Liege, Belgium