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Neurophysiological Study of tDCS Effects in Healthy Volunteers

Neurophysiological Study of tDCS Effects in Healthy Volunteers

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02125422
Acronym
tDCSHV
Enrollment
18
Registered
2014-04-29
Start date
2013-11-30
Completion date
2014-04-30
Last updated
2015-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Volunteers

Brief summary

Transcranial direct current stimulation is a tool to modulate cortical excitability.

Detailed description

Anodal transcranial direct currenti stimulation over visual cortex is able to decrease the thermo-nociceptive sensibility and thermonociceptive potentials, whilst cathodal transcranial direct current stimulation has the opposite effect, it decreases VEP amplitude and habituation. This neuromodulation technique is probably a tool in the prevention in episodic and chronic migraine. The aim of the study is to study short and long term effect of tDCS over pain treshold, contact heat evoked potentials, blink reflex and visual evoked potentials in healthy volunteers.

Interventions

Cefaly tDCS (transcranial direct current stimulation) is able to modify cortical excitability, in particular anodal tDCS increases it. The side effects of tDCS are minor, especially sensations of itching and scalp paresthesias.

Sponsors

University of Liege
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy volunteers

Exclusion criteria

* age below 18 or above 65 years * personal history of recurrent headache or other neurological diseases especially seizures, * familial history of recurrent headache * child migraine equivalents (motion sickness, cyclic vomiting or recurrent abdominal pain, somnambulism etc.. . .) * chronic pain syndromes * analgesics intake at the time of recording * contra-indications to tDCS neurostimulation (metal prosthetics in the head or internal stimulation like a pacemaker).

Design outcomes

Primary

MeasureTime frameDescription
Neurophysiological mesures changesup to 1 monthModifications in neurophysiological test after direct current stimulation

Other

MeasureTime frameDescription
VEP changesup to 1 monthEvaluation of changes in latency, amplitude, slope and habituation
Blink changesup to 1 monthEvaluation of changes in latency, amplitude, slope and habituation
CHEPS changesup to 1 monthEvaluation of changes in latency, amplitude, slope and habituation
Quantitave Sensory Testingup to 1 monthEvaluation of changes in thresholds

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026