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Clinical Trials/NCT01845129
NCT01845129
Unknown
Not Applicable

Impact of Transcranial Direct Current Stimulation of the Motor Cortex on Language Functions in Residual Aphasia

Charite University, Berlin, Germany1 site in 1 country16 target enrollmentApril 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Residual Aphasia
Sponsor
Charite University, Berlin, Germany
Enrollment
16
Locations
1
Primary Endpoint
Response latency during picture naming task (max. 80)
Last Updated
13 years ago

Overview

Brief Summary

The present study assesses whether language functions in patients with residual post-stroke aphasia can be improved by transcranial direct current stimulation administered to the primary motor cortex in the language dominant (left) hemisphere.

Detailed Description

Patients will participate in two tDCS sessions (atDCS; sham) in a cross-over within subjects design. tDCS or placebo will be administered during simulatneous fMRI to assess neural signatures of the stimulation. Order of stimulation will be counterbalanced between subjects

Registry
clinicaltrials.gov
Start Date
April 2013
End Date
April 2014
Last Updated
13 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marcus Meinzer

Creutzfeldt Fellow

Charite University, Berlin, Germany

Eligibility Criteria

Inclusion Criteria

  • right handedness
  • German native speaker
  • cerebrovascular stroke in left hemisphere (\>6 months)
  • mild aphasia (according to Aachen Aphasia Test Battery Classification, Huber et al., 1983)
  • residual anomia in naming test (\>75 correct responses)

Exclusion Criteria

  • other current or previous neurological or psychiatric diseases
  • alcohol or drug abuse
  • MRI contraindication (e.g. magnetic metal, pacemaker, claustrophobia)

Outcomes

Primary Outcomes

Response latency during picture naming task (max. 80)

Time Frame: Change in response latency between assessment 1 (week 1) and assessment 2 (week 2), assessments 1 and 2 are seperated by one week

Subjects are assessed in a cross-over design. The primary outcome measure will be assessed twice in each subject, either during placebo ("sham) stimulation or active (anodal) stimulation with transcranial direct current stimulation. Order of stimulation will be counterbalanced across the group.

Secondary Outcomes

  • Change in neural activity measured by functional magnetic resonance imaging(Change in fMRI activity between Assessment 1 (week 1) and Assessment 2 (week 2), assessments 1 and 2 are seperated by one week)

Study Sites (1)

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