Neurodoc: Sub-study of the NEURODOC Project : Neurophysiological Evaluation of a Routine Care Open Label tDCS Session

Sponsor
Groupe Hospitalier Pitie-Salpetriere (Other)
Overall Status
Completed
CT.gov ID
NCT04035655
Collaborator
(none)
66
1
1
35
1.9

Study Details

Study Description

Brief Summary

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 mechanisms by which tDCS improves consciousness are poorly understood and the electrophysiological effects of such a stimulation have never been studied in disorders of consciousness patients.

In this study, the investigators will use detailed clinical examinations and electrophysiological assessments (quantitative high-density EEG and event-related potentials) to assess the effect of a open-label single session of left dorsolateral prefrontal cortex tDCS stimulation administered as routine care.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Coma Recovery Scale - revised
  • Diagnostic Test: Electrophysiological recordings
N/A

Detailed Description

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 (1, 2, 3, 4), with no side effects reported.

However the mechanisms by which tDCS improves consciousness are poorly understood and the electrophysiological effects of the stimulation have never been studied in disorders of consciousness patients.

In this study, the investigators will use detailed clinical examinations (Coma Recovery Scale

  • Revised (5)) and electrophysiological assessments (quantitative high-density EEG and event-related potentials) (6, 7) and event-related potentials (8, 9) together with a standard morphological MRI to assess the effect of a open-label single session of left dorsolateral prefrontal cortex tDCS stimulation administered as routine care.

The primary goal is to investigate electrophysiological response to tDCS and its relation to behavioral response to better understand how tDCS affects consciousness in disorders of consciousness patients.

References:
  1. Angelakis, E. et al. Transcranial Direct Current Stimulation Effects in Disorders of Consciousness. Arch. Phys. Med. Rehabil. 95, 283-289 (2014).

  2. Thibaut, A., Bruno, M.-A., Ledoux, D., Demertzi, A. & Laureys, S. tDCS in patients with disorders of consciousness: sham-controlled randomized double-blind study. Neurology 82, 1112-1118 (2014).

  3. Thibaut, A. et al. Controlled clinical trial of repeated prefrontal tDCS in patients with chronic minimally conscious state. Brain Inj. 1-9 (2017). doi:10.1080/02699052.2016.1274776

  4. Martens, G. et al. Randomized controlled trial of home-based 4-week tDCS in chronic minimally conscious state. Brain Stimulat. (2018). doi:10.1016/j.brs.2018.04.021

  5. Giacino, J. T. & Kalmar, K. Diagnostic and prognostic guidelines for the vegetative and minimally conscious states. Neuropsychol. Rehabil. 15, 166-174 (2005).

  6. Sitt, J. D. et al. Large scale screening of neural signatures of consciousness in patients in a vegetative or minimally conscious state. Brain 137, 2258-2270 (2014).

  7. Engemann, D. A. et al. Robust EEG-based cross-site and cross-protocol classification of states of consciousness. Brain J. Neurol. 141, 3179-3192 (2018).

  8. Bekinschtein, T. A. et al. Neural signature of the conscious processing of auditory regularities. Proc. Natl. Acad. Sci. 106, 1672-1677 (2009).

  9. Faugeras, F. et al. Event related potentials elicited by violations of auditory regularities in patients with impaired consciousness. Neuropsychologia 50, 403-418 (2012).

Study Design

Study Type:
Interventional
Actual Enrollment :
66 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Electrophysiological evaluation of a routine care intervention: single session of left dorso-lateral transcranial direct current stimulationElectrophysiological evaluation of a routine care intervention: single session of left dorso-lateral transcranial direct current stimulation
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Sub-study of the NEURODOC Project (Electrophysiological Evaluation of Consciousness in Patients With Disorders of Consciousness During Standard Care Procedures): Neurophysiological Evaluation of a Routine Care Open Label tDCS Session
Actual Study Start Date :
Oct 1, 2015
Actual Primary Completion Date :
Sep 1, 2018
Actual Study Completion Date :
Sep 1, 2018

Arms and Interventions

Arm Intervention/Treatment
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.

Behavioral: Coma Recovery Scale - revised
Assessment of the level of consciousness by the dedicated Coma Recovery Scale - Revised, current gold-standard in consciousness level assessment. Assessment before and after the tDCS session (immediately before and after the electrophysiological assessment, see below).
Other Names:
  • CRS-R
  • Diagnostic Test: Electrophysiological recordings
    The electrophysiological assessment consisted of: a 5 minutes resting state high-density EEG recording a approximately 6 minutes auditory oddball paradigm These two procedures were administered immediately before and after the tDCS session
    Other Names:
  • EEG
  • Outcome Measures

    Primary Outcome Measures

    1. Support vector machine multivariate prediction of consciousness from resting state EEG markers [Two time points: immediately before (baseline) and immediately after stimulation (post-stimulation)]

      Change from baseline of the predicted probability of conscious state, ie. to be classified a in a 'minimally conscious state' as opposed to be classified as in a 'vegetative state'. The prediction will be based on a set of markers extracted from the EEG (power spectra, information theory, complexity and connectivity markers) and will use a support vector machine classifier algorithm train on a validated database. See Sitt et al., Brain et al. 2014. for details on the EEG preprocessing, markers extraction, support vector machine algorithm and training database.

    2. Evoked response potential during auditory oddball paradigm [Two time points: immediately before (baseline) and immediately after stimulation (post-stimulation)]

      Change of the Evoked Response Potentials recorded during the auditory oddball paradigm

    Secondary Outcome Measures

    1. Resting state EEG individual markers [Two time points: immediately before (baseline) and immediately after stimulation (post-stimulation)]

      In addition to the multivariate classification from the EEG, the response to stimulation will be evaluated on several quantitative markers derived from the EEG: power spectrum, complexity and connectivity assessed by the weighted symbolic mutual information (King & Sitt, Current Biology 2013; Sitt, Brain 2014; Engemann & Raimondo, Brain 2018)

    2. State of consciousness [Two time points: immediately before (baseline) and immediately after stimulation (post-stimulation)]

      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.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Groupe Hospitalier Pitié-Salpêtrière Paris France 75013

    Sponsors and Collaborators

    • Groupe Hospitalier Pitie-Salpetriere

    Investigators

    • Principal Investigator: Lionel Naccache, MD, PhD, Assistance Publique - Hôpitaux de Paris

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    LIONEL NACCACHE, Professor, Groupe Hospitalier Pitie-Salpetriere
    ClinicalTrials.gov Identifier:
    NCT04035655
    Other Study ID Numbers:
    • 2013-A01385-40
    First Posted:
    Jul 29, 2019
    Last Update Posted:
    Jul 29, 2019
    Last Verified:
    Jul 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    Yes
    Keywords provided by LIONEL NACCACHE, Professor, Groupe Hospitalier Pitie-Salpetriere
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 29, 2019