Optimizing tDCS Protocol for Clinical Use in Major Depressive Disorder

Status Completed

Clinical Trial Summary

In this project, the efficacy of different tDCS protocols in major depression will be investigated. The tDCS protocols have already been investigated in humans, and results showed that stimulation intensity has a different effect on tDCS long-term aftereffects based on the human motor cortex model. The project has three major goals: first, we want to see if the differential outcome of tDCS dosage, as present in healthy populations, can be translated to patients with major depression. Second, we want to compare the efficacy of a multi-channel novel protocol with conventional tDCS modules. Lastly, we are interested in the safety and tolerability of optimized multi-channel. The project output will be an optimized tDCS protocol for major depression treatment.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06165445
Study type	Interventional
Source	The National Brain Mapping Laboratory (NBML)
Contact
Status	Completed
Phase	N/A
Start date	June 1, 2021
Completion date	March 1, 2023

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