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TerminatedNCT03576248CONTEST_3Updated Sep 23, 2026

CONsciousness Transcranial Electric STimulation

An interventional study of In-phase 6 Hz prefronto-parietal tACS and Sham prefronto-parietal tACS in Disorder of Consciousness, sponsored by Institut National de la Santé Et de la Recherche Médicale, France. Terminated at 1 site in France. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-09-23.

Sponsored by Institut National de la Santé Et de la Recherche Médicale, France · Not applicable, Interventional, and Treatment

Why this study was terminated
Expected number of patients unreached because of COVID19 pandemics. Inclusion stopped at N=20 patients (lower expected number of patients).
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Disorder of Consciousness

Keywords

  • State of consciousness
  • tACS
  • tDCS
  • Global neuronal workspace
  • Brain injury
03

In context

Consciousness Disorders

236 studies on the registry are indexed under Consciousness Disorders; 102 are open to participants now.

This study's enrollment of 20 is below the median of 40 across 147 interventional studies indexed under Consciousness Disorders.

Browse Consciousness Disorders studies →

Lead sponsor

Institut National de la Santé Et de la Recherche Médicale, France is the lead sponsor of 375 studies on the registry; 82 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age between 18 and 80 years
  • Non communicative patients with disorder of consciousness diagnosed by CRS-R (VS, MCS, exitMCS)
  • Patients with stable clinical examination (even in intensive care)
  • Brain injury confirmed by cerebral imaging (MRI or TDM)
  • French social security affiliation
  • Signed and informed consent by the patient or by a legal representant

Exclusion criteria

Exclusion Criteria:

  • Status epilepticus or uncontrolled epilepsy
  • Severely neurodegenerative illnesses (Alzheimer disease, Lewy Body Dementia)
  • Electrical stimulation contraindication (metallic intra-cranial implants, pacemaker or implantable cardioverter-defibrillator, cranial prosthesis)
  • Pregnant, parturient or breastfeeding women- Patients underage
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    In-phase 6 Hz prefronto-parietal tACS

    6 Hz stimulation (1000 μA) with transcranial Alternative Current Stimulation (tACS) 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 of the 10-20 international scalp EEG system, with a return electrode in Cz) for 20 minutes. The phase difference between the two stimulation sites will be 0°.

    Device: In-phase 6 Hz prefronto-parietal tACS

  • Sham comparator
    Sham prefronto-parietal tACS

    The same stimulation as in in-phase transcranial Alternative Current Stimulation tACS (6 Hz F3 and P3 stimulation with 0° phase difference) will start with a current intensity of 1000 μA lasting for 30 seconds. Afterwards, the intensity will progressively decrease over 20 seconds until cessation. The whole session duration is 20 minutes.

    Device: Sham prefronto-parietal tACS

  • Experimental
    2 mA left prefrontal tDCS

    2000 μA anodal transcranial Direct Current Stimulation (tDCS) will be applied over the left prefrontal dorso-lateral cortex (F3 of the 10-20 international scalp EEG system with a right supraorbital return electrode (Fp2 of the 10-20 international scalp EEG system) during 20 minutes.

    Device: 2 mA left prefrontal tDCS

  • Sham comparator
    Sham left prefrontal tDCS

    The same stimulation as active transcranial Direct Current Stimulation (tDCS) (anodal F3 and return in Fp2) will start at 2 mA intensity for 30 seconds. Afterwards, the intensity will progressively decrease over 20 seconds until cessation. The whole session duration is 20 minutes.

    Device: Sham left prefrontal tDCS

Interventions

  • DeviceIn-phase 6 Hz prefronto-parietal tACS

    tACS is a non-invasive stimulation technique that works by delivering a weak sinusoidally oscillating electrical current to the surface of the skull to entrain oscillations in the brain.

  • DeviceSham prefronto-parietal tACS

    tACS is a non-invasive stimulation technique that works by delivering a weak sinusoidally oscillating electrical current to the surface of the skull to entrain oscillations in the brain.

  • Device2 mA left prefrontal tDCS

    tDCS is a form of neuromodulation method where very low levels of constant current are delivered to specifically targeted areas of the brain

  • DeviceSham left prefrontal tDCS

    tDCS is a form of neuromodulation method where very low levels of constant current are delivered to specifically targeted areas of the brain

06

What researchers measure

Primary outcomes

  1. State of consciousness

    Change of the Coma Recovery Scale-Revised scores (CRS-R, Giacino et al. Neurology 2002 and Kalmar et al., Neuropsychol Rehabil 2005) between before and after stimulation (CRS-R post stimulation - CRS-R before stimulation). The CRS-R score is a qualitative and quantitative scales ranking predefined behaviors elicited by the patients in the following six subscales, auditory function, visual function, motor function, verbal and oromotor function, communication and wakefulness, the sum of which give a total score ranging from 0 to 23. Higher values of the scale mean a better state of consciousness. This change in state of consciousness will be compared between active stimulation and sham stimulation

    Time frame: Two time points: immediately before (baseline) and immediately after stimulation (post-stimulation)

Secondary outcomes

  1. Evoked response potential during local-global paradigm

    Change of the ERPS recorded during the "local global" auditory paradigm (Bekinschtein et al., PNAS 2009)

    Time frame: Two time points: immediately before (baseline) and immediately after stimulation (post-stimulation)

  2. Resting state EEG

    Change from baseline of the multivariate automatic classification of conscious state from EEG (Sitt et al., Brain et al. 2014)

    Time frame: Two time points: immediately before (baseline) and immediately after stimulation (post-stimulation)

07

Study locations

1 site
  • Institut du Cerveau et de la Moelle - CR-ICM U 975 / UMRS INSERM 1127
    Paris, 75013, France
08

References and documents

Publications

  • Thibaut A, Bruno MA, Ledoux D, Demertzi A, Laureys S. tDCS in patients with disorders of consciousness: sham-controlled randomized double-blind study. Neurology. 2014 Apr 1;82(13):1112-8. doi: 10.1212/WNL.0000000000000260. Epub 2014 Feb 26. PubMed 24574549 ↗
  • Polania R, Nitsche MA, Korman C, Batsikadze G, Paulus W. The importance of timing in segregated theta phase-coupling for cognitive performance. Curr Biol. 2012 Jul 24;22(14):1314-8. doi: 10.1016/j.cub.2012.05.021. Epub 2012 Jun 7. PubMed 22683259 ↗
  • Giacino JT, Ashwal S, Childs N, Cranford R, Jennett B, Katz DI, Kelly JP, Rosenberg JH, Whyte J, Zafonte RD, Zasler ND. The minimally conscious state: definition and diagnostic criteria. Neurology. 2002 Feb 12;58(3):349-53. doi: 10.1212/wnl.58.3.349. PubMed 11839831 ↗
  • Kalmar K, Giacino JT. The JFK Coma Recovery Scale--Revised. Neuropsychol Rehabil. 2005 Jul-Sep;15(3-4):454-60. doi: 10.1080/09602010443000425. PubMed 16350986 ↗
  • Sangare A, Munoz-Musat E, Hermann B, Herault C, Belloli L, Breton M, Borden A, Ben Salah A, Valente M, Demeret S, Rohaut B, Sitt JD, Naccache L. Prefrontal tDCS modulates behavioural and neural signatures associated with consciousness. Neuroimage. 2026 Aug 1;336:122015. doi: 10.1016/j.neuroimage.2026.122015. Epub 2026 May 22. PubMed 42176825 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03576248
Lead sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Responsible party
Sponsor
First posted
Jul 3, 2018
Start date
Nov 19, 2018
Primary completion
Oct 31, 2022
Completion
Jan 3, 2024
Last update
Sep 23, 2026

Study contacts

Jacobo D Sitt, MD, PhD
principal investigator · CR-ICM U 975 /UMRS INSERM 1127
Lionel Naccache, MD, PhD
principal investigator · CR-ICM U 975 /UMRS INSERM 1127
Bertrand Hermann, MD
principal investigator · CR-ICM U 975 /UMRS INSERM 1127

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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