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Effects of tDCS on High Level and Recreational Athletes

NCT03893604 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2020-03-31

No results posted yet for this study

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

Conditions

  • Healthy
  • Athlete

Interventions

DEVICE

tDCS

20 minutes of anodal tDCS (C3/FP2) 2mA or sham

Sponsors & Collaborators

  • University of Liege

    lead OTHER

Principal Investigators

  • Stephen Bornheim, Msc · Liege University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-03-31
Primary Completion
2019-06-30
Completion
2019-06-30

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03893604 on ClinicalTrials.gov