Transcranial Direct Current Stimulation Effects in Patients With Chronic Consciousness Disorders
- Conditions
- TBIMinimally Conscious State
- Interventions
- Device: real-tDCS
- Registration Number
- NCT02288533
- Lead Sponsor
- University Hospital of Ferrara
- Brief Summary
Chronic consciousness disorders have high level of impact on public health and its costs.
- Detailed Description
Consciousness disorders have high impact on society and national health system. One of these disorders is vegetative condition in which, as in coma, there isn't any self or environmental consciousness but there is alertness, whereas in minimal state of consciousness at least part of awareness is conserved.
In Emilia Romagna region about 80 people per million of inhabitants are hospitalized after cerebral damage, and after discharge about 1/5 of patients are stabilized in a consciousness disorder.
The diagnosis of these disorders is based on neurobehavioural tests, for example JFK Coma Recovery Scale Revised (CRS-R).
In these patients recovery of state of consciousness is one of the main challenges. There are very little evidences about treatment, it has been proposed the use of therapies that could modulate central nervous system activity, like specific drugs, neuroimaging and neuromodulation techniques such as transcranial magnetic stimulation and repetitive transcranial current stimulation.
A non invasive neuromodulation technique is transcranial direct current stimulation (tDCS) which can modulate cortical excitability: cathodic current reduces excitability whereas anodic current increases it.
In conclusion, tDCS is an easy technique to use, it's not invasive and it's an efficient tool for the modulation of cortical excitability that demonstrated reliable results in healthy subjects.
As the tDCS can modulate cortical excitability it is likely that the combination of this stimulation tool with transcranial magnetic stimulation for the registration of cortical excitability could give important information about cerebral damage in patients with consciousness disorders and to test new treatments. It is also likely that the modification of cortical excitability could induce neurobehavioural changes.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 10
- males and females aged >18 years old and <70 years old
- diagnosis of disorders of consciousness classified as MCS according to criteria of American Academy of Neurology1.
- traumatic etiology (>12 months after the acute injury)
- contraindications to single pulse TMS (TMS will be used to measure cortical excitability) such as metal head implants, history of seizures, metal in the head, implanted brain medical devices.
- contraindications to tDCS such as metal in the head, implanted brain medical devices.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description real-tDCS real-tDCS Participants will receive tDCS over the primary motor cortex bilaterally (M1). The excitability-enhancing anode electrode (saline-soaked sponge electrode - 16cm2) will be placed over the primary motor cortex, C3 and C4 (10/20 international EEG system). The excitability-diminishing cathode electrode will be placed over the supraorbital area. We will use the following stimulation parameters: intensity of 2 milliampere and for 40 minutes (10 consecutive sessions).
- Primary Outcome Measures
Name Time Method Coma Recovery Scale Revised (CRS-R) Change measures (weeks: -2,0,1,2,4) behavioural scale (visual, auditory, motor, verbal, communication, arousal)
- Secondary Outcome Measures
Name Time Method single-pulse transcranial magnetic stimulation (TMS) Change measures (weeks: -2,0,1,2,4) cortical excitability measures
Circulating Biomarkers Change measures (weeks: -2,0,1,2,4) blood biomarker levels modifications
electroencephalography (EEG) Change measures (weeks: -2,0,1,2,4) To assess if, after tDCS administration, MCS patients could show: electroencephalographic pattern modifications
functional near infrared spectroscopy (fNIRS) Change measures (weeks: -2,0,1,2,4) cerebral perfusion
Trial Locations
- Locations (1)
Ferrara University Hospital
🇮🇹Ferrara, Italy