MedPath

Transcranial Direct Current Stimulation (tDCS) in the Primary Motor Cortex in Healthy Individuals

Not Applicable
Completed
Conditions
Basic Physiology
Brain Stimulation
Registration Number
NCT04148547
Lead Sponsor
Universidad Autonoma de Madrid
Brief Summary

The main aim of this study is to assess the short-term effects of active-tDCS (a-tDCS) on the M1 regarding sensorimotor variables such as discriminative sensation, pressure pain threshold and electromyographic activity compared with a sham-tDCS (s-tDCS) in healthy individuals. The main objective was to determine whether there were clinically relevant changes generated by tDCS and if they were superior to a sham intervention.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • asymptomatic participants
  • men and women aged 18 to 65 years
Exclusion Criteria
  • insomnia
  • nausea
  • headache
  • pregnancy
  • use of painkillers in the last 24 hours
  • presence of metal inside the head
  • pacemaker
  • wound on the area of electrodes' application
  • drug consumption; (j) recent application of tDCS
  • psychiatric disease impeding understanding of the study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Pressure pain threshold through an algometerChange in pressure pain threshold immediately at the end of the intervention

Pressure pain threshold has been defined as the minimal amount of pressure at which a sense of pressure first changes to pain or discomfort

Tactile acuity thresholdChange in tactile acuity threshold immediately at the end of the intervention

Tactile acuity threshold is an important variable to know the somatosensory state and Von Frey monofilaments and Aesthesiometer were used

Muscle recruitment through electromyographic activityChange in electromyographic activity immediately at the end of the intervention

The activity of surface electromyography (sEMG) during an isometric maximal voluntary contraction was measured in the biceps brachii and rectus femoris.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

CSEU La Salle

🇪🇸

Madrid, Spain

CSEU La Salle
🇪🇸Madrid, Spain

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.