Disorder of Consciousness Clinical Trial
Official title:
Effect of Transcranial Electrical Stimulation on the Consciousness of Non-communicating Patients.
The aim of this study is to investigate the effect of transcranial Alternating Current
Stimulation (tACS) at theta frequency and the the effect of transcranial Direct Current
Stimulation (tDCS) on the conscious state of non-communicating patients. tACS and tDCS are
non-invasive stimulation techniques that are used to induce brain oscillations at certain
frequency or to increase the brain activity in applied region.
Limited treatments are available to improve consciousness in severely brain injured patients.
Transcranial Direct Current stimulation (tDCS) is one of the few therapeutics that showed
evidence of efficacy to increase level of consciousness and functional communication in some
Minimally Conscious State (MCS) patients, and in some Vegetative State (VS) patients. However
the optimal intensity of electrical current stimulation remains unknown and transcranial
Alternative Current Stimulation (tACS), with the ability to stimulate cortex at specific
frequencies and to manipulate phase-synchrony between regions is a promising techniques to
improve patients' consciousness.
In this study, the investigators will use prefrontal tDCS and theta tACS to improve patients
consciousness level.
This study is constituted of two independent sub-studies investigating two types of
stimulation (tDCS and tACS) with the same cross-over design
Study design The study design is composed of two experimental sessions, one active
stimulation and one sham comparator. Sessions will be randomized in a double-blind randomized
crossover design (neither the participant nor the experimenter knows which session includes
which stimulation type), with at least 2 days of interval between them.
In these sessions, the patients' state of consciousness participants will first be determined
using the dedicated Coma Recovery Scale - Revised (Giacino, Neurology 2002) (CRS-R) scale
before stimulation. Resting state brain activity EEG and cognitive auditory paradigm
(local-global paradigm, Bekinschtein, PNAS 2009) will also be recorded before stimulation.
Twenty minutes stimulation will then be performed (see below). CRS-R, resting state EEG and
local-global paradigm will be repeated after stimulation.
Outcome measures will be the same in the two studies. The primary outcome will be the change
of CRS-R between before and after stimulation. Secondary outcomes will be the
neurophysiological correlates of consciousness in resting state EEG and during the local
global paradigm.
tACS stimulation During tACS sessions, 6 Hz stimulation (1000 μA) will be applied
simultaneously over the left prefrontal dorso-lateral cortex (F3 of the 10-20 international
scalp EEG system) and the left parietal cortex (P3) using an 8-channels stimulator (Starstim
NE, Neuroelectrics, Barcelona, Spain) with small round sponge electrodes (25 cm2 surface,
maximal current density of 0.06 μA/cm2), controlled via Bluetooth. In the in-phase condition,
the phase difference between the two stimulation sites will be 0° which will entrain
synchronization between sites. In the sham condition, the stimulation will start with a
current intensity of 1000 μA lasting for 30 seconds. Afterwards, the intensity will
progressively decrease over 20 seconds until cessation. Each stimulation session will take 20
minutes and the positions of stimulation electrodes and the duration of the stimulation will
be kept identical for all conditions.
tDCS stimulation During tDCS session, 2000 μA stimulation will be applied over the left
prefrontal dorso-lateral cortex (F3 of the 10-20 international scalp EEG system) (Starstim
NE, Neuroelectrics, Barcelona, Spain) with small round sponge electrodes (25 cm2 surface,
maximal current density of 0.06 μA/cm2), controlled via Bluetooth. In the sham condition, the
stimulation will start with a current intensity of 2000 μA lasting for 30 seconds.
Afterwards, the intensity will progressively decrease over 20 seconds until cessation. Each
stimulation session will take 20 minutes and the positions of stimulation electrodes and the
duration of the stimulation will be kept identical for all conditions.
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