HD-tDCS: Effects on the Somatosensory System

Status Completed

Clinical Trial Summary

The purpose of this study is to investigate the efficacy of high definition tDCS on different cortical targets in modulating the nociceptive system in the healthy subjects.

Clinical Trial Description

The investigators aim to investigate the efficacy of different HD-tDCS electrode configurations on modulating the somatosensory/nociceptive system.

This is done to investigate the hypothesis, that different stimulation protocols can be used to modulate the somatosensory and nociceptive system, as shown in the previous studies, but that it is necessary to uncover the most efficient way to do so.

The study uses a double-blinded, sham-controlled, longitudinal design, where quantitative sensory testing will be used to assess the somatosensory function of the participants before and after a receiving a specific configuration of HD-tDCS on three consecutive days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04165876
Study type	Interventional
Source	Aalborg University
Contact
Status	Completed
Phase	N/A
Start date	December 18, 2018
Completion date	March 18, 2020

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