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Different Montages of Transcranial Direct Current Stimulation Tongue Strength

U

University of Liege

Status

Unknown

Conditions

Healthy

Treatments

Device: Transcranial Direct Current Stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT04343612
2020-93

Details and patient eligibility

About

20 healthy subjects will be split into 4 groups. Each group will receive one of the following tDCS montages : anodal, bilateral, cathodal or placebo Subjects will receive 2mA for 20 mins of their attributed tDCS. The evaluation is a maximal strength test measured with the IOPI and will take place prior to, immediately following and 30 minutes after stimulation

Enrollment

20 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy

Exclusion criteria

  • One Yes on the medium and high risk sections of the TSST (Bornheim et al.,2019)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

20 participants in 4 patient groups, including a placebo group

Anodal
Experimental group
Description:
Anode placer over the affected primary motor cortex, cathode over contralateral supra orbital area. 2 mA, 20min stimulation
Treatment:
Device: Transcranial Direct Current Stimulation
Bilateral
Experimental group
Description:
Anode placer over the affected primary motor cortex, cathode over unaffected motor cortex. 2 mA, 20min stimulation
Treatment:
Device: Transcranial Direct Current Stimulation
Cathodal
Experimental group
Description:
Cathode placer over the unaffected primary motor cortex, anode over contralateral supra orbital area. 2 mA, 20min stimulation
Treatment:
Device: Transcranial Direct Current Stimulation
Placebo
Placebo Comparator group
Description:
anode montage but current is ramped up over 15 secondes, then ramped down. 2 mA, 20min stimulation
Treatment:
Device: Transcranial Direct Current Stimulation

Trial contacts and locations

1

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Central trial contact

Stephen Bornheim, Msc

Data sourced from clinicaltrials.gov

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