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Clinical Trials/NCT02101398
NCT02101398
Terminated
Not Applicable

Etude de l'Effet de Stimulations transcrâniennes en Courant Continu (tDCS) Sur Les Performances en dénomination Chez le Sujet Aphasique à Moins d'un an de Son Accident Vasculaire cérébral : Comparaison de 5 Configurations de Stimulation

Institut National de la Santé Et de la Recherche Médicale, France1 site in 1 country5 target enrollmentOctober 2, 2014
ConditionsAphasiaStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aphasia
Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Enrollment
5
Locations
1
Primary Endpoint
Percentage of improvement of picture naming
Status
Terminated
Last Updated
8 months ago

Overview

Brief Summary

The aim of this work is to study the effect of transcranial direct current stimulation combined with naming therapy in acute and post-acute stroke comparing four bihemispheric positioning electrodes to a sham condition.

Detailed Description

TDCS have shown a positive effect on clinical outcome in naming treatment in aphasic subjects however some aspects as the positioning of the electrodes on the head are still unclear. That is why we compare the effects of four different positionings of the electrodes (two anterior over Broca's area and its homologue and two posterior over Wernicke's area and its homologue) to a sham stimulation in order to observe if a more important effect of one or another positioning could be found.

Registry
clinicaltrials.gov
Start Date
October 2, 2014
End Date
July 1, 2016
Last Updated
8 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • man or woman of 18 years and older
  • aphasic patient following a first left hemispheric stroke
  • BDAE 3.0 aphasia score \> or = to 1
  • stroke within 3 to 12 months before inclusion in the study
  • mother tongue = French
  • right handedness
  • signed informed consent

Exclusion Criteria

  • history of other neurologic pathologies
  • epileptic seizure within 2 months before inclusion
  • bilingual patient (2 mother tongues)
  • history of cranial surgery
  • presence of intracerebral metallic material
  • unauthorized molecules at inclusion : sulpiride, rivastigmine, dextromethorphan, carbamazepine, flunarizine, levodopa
  • pregnant, parturient or lactating woman

Outcomes

Primary Outcomes

Percentage of improvement of picture naming

Time Frame: Before stimulation and immediately after stimulation

Study Sites (1)

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