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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03901508
Other study ID # 2017/29
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 5, 2019
Est. completion date June 5, 2019

Study information

Verified date March 2020
Source University of Liege
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Healthy recreational athletes will undergo a session of anodal tDCS (transcranial direct current stimulation) or sham tDCS.

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


Description:

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

Each subject came 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 underwent a concentric and eccentric isokinetic test of their lower limbs (dominant or non-dominant side depending on their group). Subjects then received either anodal tDCS, of sham tDCS. Neither the evaluator or the subject knew which they were receiving. Immediately following tDCS, there was a another isokinetic test, and 30 minutes after the second test, a subjects underwent a third test.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 5, 2019
Est. primary completion date June 5, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Between 3 and 5 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


Related Conditions & MeSH terms


Intervention

Device:
TDCS
20 minutes, 2 electrodes (C3/FP2)

Locations

Country Name City State
Belgium Liege Univeristy Hospital Liege

Sponsors (1)

Lead Sponsor Collaborator
University of Liege

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Isokinetic Peak Strength Concentric and Eccentric Peak Strength is measured in hamstrings and quadriceps at 60°/s using an isokinetic dynamometer Changes between prior to tDCS, immediately following tDCS and 30 minutes after tDCS
Primary Isokinetic Work Concentric and Eccentric Work is measured in hamstrings and quadriceps at 60°/s using an isokinetic dynamometer Changes between prior to tDCS, immediately following tDCS and 30 minutes after tDCS
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