NCT01500564View on ClinicalTrials.gov

Functional Interest of Non Invasive Brain Stimulation During Physiotherapy at a Subacute Phase Post Stroke (Anodal Protocol): ReSTIM

NACompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

January 2, 2012

Primary Completion Date

July 31, 2015

Study Completion Date

July 31, 2015

Conditions
Stroke
Interventions
DEVICE

anodal tDCS (device) Eldith DC-Stimulator

tDCS applied to the motor cortex every day of two consecutive weeks (10 sessions) at 1 mA during 20 minutes. Conductive rubber covered by sponges soaked in saline will be used, held in place by a band. The current will be gradually increased over 100 seconds.

DEVICE

Sham tDCS

Participants will receive sham tDCS over the primary motor cortex of the ipsilesional hemisphere during 20 minutes of motor training (10 consecutive sessions Monday-Friday during two weeks).

Trial Locations (2)

54690

Centre de Lay-Saint-Christophe-Institut Régional de Médecine Physique et de Réadaptation, Lay-Saint-Christophe

69235

Hospices Civils de Lyon- Hôpital Henry Gabrielle-Service de Médecine Physique et Réadaptation, Saint-Genis-Laval

All Listed Sponsors
lead

Hospices Civils de Lyon

OTHER

NCT01500564 - Functional Interest of Non Invasive Brain Stimulation During Physiotherapy at a Subacute Phase Post Stroke (Anodal Protocol): ReSTIM | Biotech Hunter | Biotech Hunter