ClinicalTrials.Veeva

Menu

Effects of tDCS on High Level and Recreational Athletes

U

University of Liege

Status

Completed

Conditions

Athlete
Healthy

Treatments

Device: tDCS

Study type

Interventional

Funder types

Other

Identifiers

NCT03893604
2017-313

Details and patient eligibility

About

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

Full 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.

Enrollment

60 patients

Sex

Male

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

60 participants in 2 patient groups

Anodal tDCS
Experimental group
Description:
Subjects will receive 20min anodal tDCS
Treatment:
Device: tDCS
Sham tDCS
Sham Comparator group
Description:
Subjects will receive 20 minutes of Sham anodal tDCS
Treatment:
Device: tDCS

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems