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Clinical Trials/NCT01652391
NCT01652391
Completed
Not Applicable

Modulation of Cognitive Control in Healthy and Depressed Subjects by Transcranial Direct Current Stimulation

University Hospital Tuebingen1 site in 1 country44 target enrollmentJuly 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Major Depression
Sponsor
University Hospital Tuebingen
Enrollment
44
Locations
1
Primary Endpoint
Correctness of response
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Insufficient cognitive control over emotional distracters is characteristic for major depressive disorder (MDD). Hypoactivation of the dorsolateral prefrontal cortex (dlPFC) is associated with this deficit. In this study the investigators assess the effect of an enhancement of dlPFC activity in MDD patients by anodal transcranial direct current stimulation (tDCS) on cognitive control.

In a double-blinded, balanced randomized, sham-controlled crossover trial the investigators determine the effect of a single-session tDCS to the left dlPFC on cognitive control in MDD patients and healthy controls. To assess the cognitive control the investigators use a delayed response working memory (DWM) task with pictures of varying valence presented during the delay period.

Registry
clinicaltrials.gov
Start Date
July 2011
End Date
December 2012
Last Updated
12 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christian Plewnia, MD

Professer

University Hospital Tuebingen

Eligibility Criteria

Inclusion Criteria

  • age \> 18
  • informed consent
  • in the patients group: Major depressive disorder, no antidepressant medication or stability over 1 week

Exclusion Criteria

  • cardiac pacemaker
  • deep brain stimulation

Outcomes

Primary Outcomes

Correctness of response

Time Frame: The primary outcome measure is obtained during the intervention (20min tDCS or sham stimulation).

Secondary Outcomes

  • Reaction time(The secondary outcome measure is obtained during the intervention (20min tDCS or sham stimulation).)

Study Sites (1)

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