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Clinical Trial Summary

Noninvasive brain stimulations (NIBS) will be used in MS patients with cognitive impairments to enhance their cognitive aptitudes.


Clinical Trial Description

tDCS will be used in a sham-controlled, double-blind, randomized, cross-over control trial in MS patients suffering from cognitive impairments and/or motor deficits. After informed consent and recruitment, patients will be randomly (computer method) allocated to real or sham tDCS, that will be applied during working memory and attentional tasks. A few days/weeks after completing one arm, the patients will enter the other arm (double-blind cross-over design). Baseline and follow-up outcomes about cognitive aptitudes, motor tasks and fatigue will be collected. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02266121
Study type Interventional
Source University Hospital of Mont-Godinne
Contact
Status Terminated
Phase N/A
Start date October 2014
Completion date May 8, 2023

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