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NCT06469463Completed

Decoding Motor Imagery From Non-invasive Brain Recordings as a Prerequisite for Innovative Motor Rehabilitation Therapies

Source: ClinicalTrials.gov · Last updated 28 Jul 2026

Brief summary (registry, in English)

Seminal studies in motor neuroscience involving healthy subjects have revealed time-locked changes in induced power within specific frequency bands. Brain recordings were shown to exhibit a gradual reduction in signal power, relative to baseline, in the mu and beta frequency bands during an action or during motor imagery: the event-related desynchronization (ERD). This is considered to reflect processes related to movement preparation and execution and is particularly pronounced in the contralateral sensorimotor cortex. Shortly following the completion of the task, a relative increase in power, the event-related synchronization (ERS), could be observed in the beta band. ERS is thought to reflect the re-establishment of inhibition in the same area. Ever since the characterization of the ERD and ERS phenomena, there has been little to no discussion in the field of non-invasive Brain Computer Interfaces (BCI) as to whether these features accurately capture the task-related modulations of brain activity. Recent studies in neurophysiology have demonstrated that the ERD and ERS patterns only emerge as a result of averaging signal power over multiple trials. On a single trial level, beta band activity occurs in short, transient events, bursts, rather than as sustained oscillations. This indicates that the ERD and ERS patterns reflect accumulated, time-varying changes in the burst probability during each trial. Thus, beta bursts may carry more behaviourally relevant information than averaged beta band power. Studies in humans involving arm movements have established a link between the timing of sensorimotor beta bursts and response times before movement, as well as behavioural errors post-movement. Beta burst activity in frontal areas has also been shown to correlate with movement cancellation and recent studies show that activity at the motor unit level also occurs in a transient manner, which is time-locked to sensorimotor beta bursts. Although beta burst rate has been shown to carry significant information, it still comprises a rather simplistic representation of the underlying activity. Indeed, complex burst waveforms are embedded in the raw signals, and can be characterized by a stereotypical average shape with large variability around it. The waveform features are neglected in standard BCI approaches, because conventional signal processing methods generally presuppose sustained, oscillatory and stationary signals, and are thus inherently unsuitable for analysing transient activity. In contrast to beta, activity in the mu frequency band is oscillatory even in single trials. This activity is typically analysed using time-frequency decomposition techniques, which assume that the underlying signal is sinusoidal. However, there is now growing consensus that oscillatory neural activity is often non-sinusoidal and that the raw waveform shape can be informative of movement. In this project, the design of a subject-specific neurophysiological model to guide motor BCI training will be optimized using Magnetic Resonance Imaging (MRI) and Magnetoencephalography (MEG) for high spatial and biophysical specificity in the experimental group. Anatomical MR volumes will be used to design and 3D-print an individual head cast that will be used in the MEG scanner to stabilize the head position and minimize movements. This high-precision approach (hpMEG) has been proven to significantly improve source localization up to the level of distinguishing laminar activity, which makes it superior to EEG recording technique. An individualized hpMEG approach, as well as the widely adopted EEG, will be used to study bursts of oscillatory activity in the beta and mu frequency bands related to motor imagery and motor execution. hpMEG will yield subject-specific models of motor imagery that will be used to constrain online decoding of EEG data. This approach will be applied and validated on a group of healthy adult subjects and will then be compared against another feasibility group of patients and age-matched healthy participants. The proposed approach will be compared with a classic EEG-based BCI approach. The information will be used to optimally guide subsequent EEG-based BCI training in the control group. After a thorough investigation in healthy subjects in this project, the feasibility of the approach will be evaluated in a few stroke patients with upper-limb motor deficits. Tasks 1.1 and 1.2 aim to develop subject-specific generative models decoding movement onset and offset, the type of movement, as well as finely discretized movement amplitude during both real and imagined wrist extensions/flexions. Task 1.2 investigates how lesions of patients alter our ability to decode attempted wrist movements.

Status (registry)
Completed
Study type
Interventional
Enrollment
30 (actual)
First submitted
28 May 2024
Start date
17 Mar 2026
Primary completion date
7 Jul 2026
Lead sponsor
Hospices Civils de Lyon
Diseases
Stroke
NCT number
NCT06469463

What you commit to

  • Study type: Interventional
  • Participants enrolled: 30
  • From 17 Mar 2026 to the primary completion date, 7 Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subjects who:
    • have had an MRI within 2 weeks prior to the experiment.
    • have implanted materials (any dental apparatus containing metal including or root canals or any metallic object, pacemaker, cochlear implanted in the body).
  • Subjects with alcohol dependence (no consumption of alcohol or drugs at least 24 hours prior to the day of experiments).
  • Subjects currently taking a medication that may have a strong effect on MEG or EEG recordings (e.g., antidepressants, stimulant medication, etc).
  • Cochlear implants or other hearing aids.
  • Intracerebral / surgical aneurysm clips.

Other illness

  • Subjects with motor impairment (only applies to control group), severe traumatic brain injury.
  • Subjects with chronic stroke (applies to both groups).
  • Subjects history of skin disease or skin allergies (multiple or severe).

Age

  • Subjects under 18 years of age.

Other

  • Subjects with characteristics incompatible with MEG and MRI :
    • 1\. Claustrophobia.
  • Subjects working with metals in their professional lives.
  • Pregnant or lactating women Pregnant or lactating women (check with a urinary test).
  • Subjects who are not able to tolerate sitting for longer than 2 hours (the estimated length of an experimental session is about 2h30mins).
  • Subjects who, in the opinion of the investigator, are not able or willing to comply with the protocol.
  • Persons under guardianship or curatorship.
  • Persons in emergency situations who cannot give their consent.
  • Subjects under legal protection measures.
  • Volunteers with contraindications to MEG examination
  • Pacemaker.
  • Implanted pump including insulin pump.
  • Neurostimulator.
  • Metal prosthesis.
  • Ocular or cerebral ferromagnetic foreign bodies in the upper body.
  • Neurosurgical ventriculoperitoneal shunt valves.

Who the study is looking for

  • Control group:
  • Healthy subjects with age\> 18, male or female.
  • Right handed (Due to the fact that unlike right-handed people, left-handed people tend to have more complicated somatotopic organization of the motor cortex, we will avoid confounding observed differences to differences attributable to anatomic factors).
  • Registered with the French healthcare system.
  • Motivated to participate in the study.
  • Normal or corrected vision.
  • Adequate knowledge of French language to be able to follow directions.
  • Subjects must be able to listen and understand the study instructions.
  • Subjects must be able to give written informed consent before participation.
  • No history of neurological or psychiatric disease.
  • No physical disability of the arms or wrists.
  • No use of drugs affecting the central nervous system or self-reported abuse of any drugs.
    • Patient group :
  • Male or female stroke patients over 18 years old.
  • Stroke patients must be not be in the acute phase of stroke.
  • Right-handed.
  • Having motor disorders in at least one of the upper limbs following the stroke, possibly with moderate accompanying deficits but no cognitive deficits.
  • Entitled to a social security scheme.
  • Motivated to participate in the study.
  • Having normal or corrected vision.
  • Having a sufficient understanding of the French language to be able to follow directions.
  • Able to listen and understand study instructions.
  • Able to give their written informed consent before participating.

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre de Recherche en Neurosciences de Lyon - INSERM U1028
Coordinator of this site? Confirm its status
BronFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.