About this trial
The goal of this clinical study is to investigate the potential synergy between non-invasive brain and spinal cord stimulation administered during a cognitive-motor task, in terms of their immediate effects on sensorimotor and cognitive functions after neurological injuries affecting the upper limb (cervical spinal cord injury and stroke). Secondary objectives are to evaluate the relevance of anatomical MRI, functional MRI, and neurophysiological measurements for optimizing and predicting the effects of these different interventions.
Eligibility criteria
Qualifiers
Over 18 years of age
Participant who has signed an informed consent form
Participant who is affiliated with and covered by the social security system
Over 18 years of age
Disqualifiers
Suffering from a chronic condition
Skin problems or open wounds
History of epilepsy or seizures
Presence of a contraindication to the use of magnetic/electrical stimulation or MRI, including: cardiac pacemaker; implanted hearing aid; intraocular foreign body, shrapnel, or bullets; metal worker; pacemaker or neurostimulator; claustrophobia
Trial design
Treatments tested in this trial
- tDCS
- tSCS
- Sham
- Cognitive-Motor Task
Treatment groups
Sponsors and collaborators
Centre National de la Recherche Scientifique, France
Lead sponsor
University Hospital, Bordeaux
Collaborator
Centre de la Tour de Gassies
Collaborator
Institute of Neurodegenerative Diseases, CNRS UMR 5293
Collaborator