Viewing Study NCT04577768



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Last Modification Date: 2024-10-26 @ 1:46 PM
Study NCT ID: NCT04577768
Status: COMPLETED
Last Update Posted: 2020-10-08
First Post: 2020-09-23

Brief Title: The Effect of Transcranial Direct Current Stimulation on Motor Performance in Healthy Adults
Sponsor: Ariel University
Organization: Ariel University

Study Overview

Official Title: The Effect of Transcranial Direct Current Stimulation Intensity on Motor Performance in Healthy Adults
Status: COMPLETED
Status Verified Date: 2020-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: to investigate the effect of stimulation intensity on motor performance in healthy adults
Detailed Description: 60 healthy subjects were randomly allocated to one of three groups a 20-min of High-Definition transcranial direct current stimulation HD-tDCS with an intensity of 2 mA HD-tDCS 2 mA 2 20-min of HD-tDCS with an intensity of 15 mA HD-tDCS 15 mA and 3 20-min of sham HD-tDCS HD-tDCS sham The stimulation was administered noninvasively using an M x N 9-channel high definition transcranial electrical current stimulator from Soterix Medical New York NY The anodal stimulation targeted the right Brodmann area 4 primary motor cortex based on HD-Targets brain modelling software Soterix Medical New York NY

Tests The non-dominant left arm was tested The subjects performed a sequential point-to-point movement task on the graphics tablet Initially the participants were required to perform 3 sequences without errors to familiarize themselves with the setup the task and the sequence Then they performed the pre-test which consisted of two blocks of 6 sequences ie 12 sequences with a 30 s break between blocks Two min after starting the appropriate stimulation they performed 2 blocks of 6 sequences identical to the pre-test After finishing the tDCS stimulation the participants performed a post-test which was also identical to the pre-test The participants returned after 24 hours to perform a retention test which was equivalent to the pre- and post-tests Two outcome measures were used movement time s and the reaction time s of the reaching movements

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None