Sub-study of the NEURODOC Project : Neurophysiological Evaluation of a Routine Care Open Label tDCS Session (Neurodoc)
Disorder of Consciousness, Traumatic Brain Injury, Anoxic Brain Injury
About this trial
This is an interventional basic science trial for Disorder of Consciousness focused on measuring Disorders of consciousness, Transcranial direct current stimulation, Electroencephalography, Electrophysiological signatures of consciousness, Coma Recovery Scale - Revised
Eligibility Criteria
Inclusion Criteria:
- Age between 18 and 80 years
- Disorder of consciousness assessed by CRS-R (VS, MCS, exitMCS)
- Patients with stable clinical examination (even in intensive care unit)
- Structural brain injury confirmed by cerebral imaging (MRI or TDM)
Exclusion Criteria:
- Refractory status epilepticus
- Known preexisting severe neurodegenerative disease (ie: Alzheimer disease, Lewy body dementia, ...)
- MRI contraindication: metallic intra-cranial implants, pacemaker or implantable cardioverter-defibrillator, cranial prosthesis
- Pregnant, parturient or breastfeeding women
Sites / Locations
- Groupe Hospitalier Pitié-Salpêtrière
Arms of the Study
Arm 1
Experimental
Clinical and electrophysiological evaluation of tDCS session
In this prospective case-control study, the investigator's main goal was to evaluate the impact of a single standard-care tDCS session on brain activity (EEG). The effect of a single 20 minutes 2 mA tDCS session with the anode placed over the left dorsolateral prefrontal cortex and the cathode over the right supraorbital cortex administered as routine care were evaluated by combined behavioral and electrophysiological assessments immediately before and after the stimulation. The study consisted of the following interventions, administered immediately before and after the stimulation session: detailed behavioral assessment by the Coma Recovery Scale-Revised (CRS-R) 5 minutes resting state high-density EEG recordings and 6 minutes auditory oddball paradigm immediately. Additionally, clinical anatomical MRI (T1) acquired as routine care were used to model the estimated tDCS-induced electric fields in the entire head of patients, based on available T1-weighted MRI.