Stroke SequelaeMODECONCT06469463
Decoding Motor Imagery From Non-invasive Brain Recordings as a Prerequisite for Innovative Motor Rehabilitation Therapies
A study testing MRI, MEG and EEG in people with Stroke Sequelae and Motor Imagery, run by Hospices Civils de Lyon at 1 site in France.
Trial summary
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… Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Stroke Sequelae, Motor Imagery, Upper Limb Deficit
- What is being tested?
- MRI, MEG and EEG
- Type of treatment
- Medical device
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 30 participants
- Where
- 1 siteFrance
- Study dates
- 17 Mar 2026to 7 Jul 2026
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- 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.
Show all 23Show fewer
- 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.
Who cannot join
- Subjects with characteristics incompatible with MEG and MRI :
- 1. Claustrophobia.
- 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).
- Subjects who:
Show all 27Show fewer
- 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 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 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).
- 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 18 years of age.
- Subjects under legal protection measures.
- Volunteers with contraindications to MEG examination
- Pacemaker.
- Implanted pump including insulin pump.
- Neurostimulator.
- Cochlear implants or other hearing aids.
- Metal prosthesis.
- Intracerebral / surgical aneurysm clips.
- Ocular or cerebral ferromagnetic foreign bodies in the upper body.
- Neurosurgical ventriculoperitoneal shunt valves.
Trial locations and contacts
1 site in 1 country.
France1 site
Centre de Recherche en Neurosciences de Lyon - INSERM U1028
Bron, 69675
About this study
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.
Read more
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.
Read the detailed description
Seminal studies in motor neuroscience involving healthy subjects have, since a long time, revealed time-locked changes in induced power within specific frequency band. Brain recordings were shown to exhibit a gradual reduction in signal power, relative to baseline, in the mu (~ 8-12 Hz) and beta (~ 13-30 Hz) frequency bands during an action or during motor imagery (MI): the so-called event-related desynchronization (ERD). This phenomenon is considered to reflect processes related to movement preparation and execution, and is particularly pronounced in the contralateral sensorimotor cortex. Moreover, shortly following the completion of the task a relative increase in power, the event-related synchronization (ERS) (also referred to as the beta rebound), 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 non-invasive BCI field as to whether these features accurately capture the task-related modulations of brain activity. Recent studies in neurophysiology have challenged this view and 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, termed 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 behaviorally relevant information than averaged beta band power. Indeed, studies in humans involving arm movements have established a link between the timing of sensorimotor beta bursts and response times prior to movement, as well as behavioral 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. Every burst can be characterized by a set of TF-based features: the burst peak time and peak frequency, as well as its duration and its span in the frequency axis. In turn, all these descriptors are extracted using a particular time-frequency transformation and constitute simpler representations of the more complex burst waveform that is embedded in the raw signals, and which is 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 analyzing transient activity.
In contrast to beta, activity in the mu frequency band is oscillatory even in single trials. This activity is typically analyzed 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. Future efforts could take advantage of this possibility by using recently developed non-parametric cycle-by-cycle analyzes.
In this project, the investigators will optimize the design of a subject-specific neurophysiological model to guide motor BCI training, by 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 in order to stabilize the subject's 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 a superior-to-EEG recording technique. In MODECO the investigators will use an individualized hpMEG approach, as well as the widely adopted EEG, 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 (control group) and will then be compared against another feasibility group of patients (patient group) and age-matched healthy participants (control group; the investigators will attempt to recruit patients relatives). the investigators will compare the proposed approach with a classic EEG-based BCI approach.
the investigators will investigate how to use this information to optimally guide subsequent EEG-based BCI training in the control group. After a thorough investigation in healthy subjects in this project, the investigators will be able to evaluate this approach on a population of stroke patients with upper-limb motor deficits. Two tasks have been designed in this project tasks 1.1 and task 1.2. The aim of Task 1.1 is to develop subject-specific generative models decoding movement onset and /offset, the type of movement (left versus right), as well as finely discretized movement amplitude during both real and imagined wrist extension/flexion movements. In task 1.2 the investigators aim to investigate how the lesions of patients alter our ability to decode attempted wrist movements (control vs patients group).
- Conditions
- Stroke Sequelae, Motor Imagery, Upper Limb Deficit
- Being tested
- MRI, MEG, EEG
- Keywords
- Motor imagery, motor rehabilitation, magnetoencephalography, electroencephalography
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
MRIDevice
The healthy subjects in the control group will perform an MRI head scan, which will be used to construct 3D head models and headcasts.
MEGDevice
The healthy subjects will undergo hpMEG data while wearing 3D-printed headcasts created from high resolution MRI
EEGDevice
The healthy participants will undergo a similar session using EEG recording, using a Polhemus Fastrak system for localization of EEG electrodes and precise co-registration with anatomy and hpMEG data.
The patients group will take part in the same EEG recording session.
| Study group | Role | What they receive |
|---|---|---|
| Control group | Placebo comparator | Control group of healthy subjects Receives: Device: MRI; Device: MEG; Device: EEG |
| Patients group | Active comparator | Patients group of post-stroke with upper-limb deficits on one side Receives: Device: EEG |
What is being measured
The primary outcome is the main question the study is designed to answer.
Develop subject-specific generative models
Movement Onset and Offset Detected During Real and Imagined Wrist Extension/Flexion Movements.
Direction of Movement Detected During Real and Imagined Wrist Extension/Flexion Movements.
Amplitude of Movement Measured During Real and Imagined Wrist Extension/Flexion Movements.
Each of these outcome measures focuses on a specific aspect of the movement, providing all the necessary information to developp subject-specific generative models.
Measured: 2 years
Secondary outcomes (1)
Beta burst characterization.
Timing of Beta Bursts Measured in MEG \& EEG Recordings. Location of Beta Bursts Measured in MEG \& EEG Recordings. Waveform Shape of Beta Bursts Measured in MEG \& EEG Recordings.
Measured: 2 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Jun 2024
- Study start17 Mar 2026
- Primary completion7 Jul 2026
- Study completion7 Jul 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Stroke SequelaeStudies of the same condition, open and under way.
- More trials run by Hospices Civils de LyonThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- Hospices Civils de Lyon
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06469463
- Sponsor's protocol ID
- 69HCL23_1346
- Other IDs
- 2024-A00161-46
- Acronym
- MODECO
- Status last verified
- Jul 2026
- First submitted
- 28 May 2024
- Last updated
- 28 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Decoding Motor Imagery From Non-invasive Brain Recordings as a Prerequisite for Innovative Motor Rehabilitation Therapies
- ClinicalTrials.gov ID
- NCT06469463
- Acronym / sponsor ID
- MODECO / 69HCL23_1346
- Conditions
- Stroke Sequelae, Motor Imagery, Upper Limb Deficit
- Keywords
- Motor imagery, motor rehabilitation, magnetoencephalography, electroencephalography
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- Hospices Civils de LyonUniversity, hospital or other
- Study start
- 17 Mar 2026 (actual)
- Primary completion
- 7 Jul 2026 (actual)
- Study completion
- 7 Jul 2026 (actual)
- First posted
- 21 Jun 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Seminal studies in motor neuroscience involving healthy subjects have, since a long time, revealed time-locked changes in induced power within specific frequency band. Brain recordings were shown to exhibit a gradual reduction in signal power, relative to baseline, in the mu (~ 8-12 Hz) and beta (~ 13-30 Hz) frequency bands during an action or during motor imagery (MI): the so-called event-related desynchronization (ERD). This phenomenon is considered to reflect processes related to movement preparation and execution, and is particularly pronounced in the contralateral sensorimotor cortex. Moreover, shortly following the completion of the task a relative increase in power, the event-related synchronization (ERS) (also referred to as the beta rebound), 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 non-invasive BCI field as to whether these features accurately capture the task-related modulations of brain activity. Recent studies in neurophysiology have challenged this view and 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, termed 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 behaviorally relevant information than averaged beta band power. Indeed, studies in humans involving arm movements have established a link between the timing of sensorimotor beta bursts and response times prior to movement, as well as behavioral 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. Every burst can be characterized by a set of TF-based features: the burst peak time and peak frequency, as well as its duration and its span in the frequency axis. In turn, all these descriptors are extracted using a particular time-frequency transformation and constitute simpler representations of the more complex burst waveform that is embedded in the raw signals, and which is 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 analyzing transient activity.
In contrast to beta, activity in the mu frequency band is oscillatory even in single trials. This activity is typically analyzed 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. Future efforts could take advantage of this possibility by using recently developed non-parametric cycle-by-cycle analyzes.
In this project, the investigators will optimize the design of a subject-specific neurophysiological model to guide motor BCI training, by 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 in order to stabilize the subject's 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 a superior-to-EEG recording technique. In MODECO the investigators will use an individualized hpMEG approach, as well as the widely adopted EEG, 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 (control group) and will then be compared against another feasibility group of patients (patient group) and age-matched healthy participants (control group; the investigators will attempt to recruit patients relatives). the investigators will compare the proposed approach with a classic EEG-based BCI approach.
the investigators will investigate how to use this information to optimally guide subsequent EEG-based BCI training in the control group. After a thorough investigation in healthy subjects in this project, the investigators will be able to evaluate this approach on a population of stroke patients with upper-limb motor deficits. Two tasks have been designed in this project tasks 1.1 and task 1.2. The aim of Task 1.1 is to develop subject-specific generative models decoding movement onset and /offset, the type of movement (left versus right), as well as finely discretized movement amplitude during both real and imagined wrist extension/flexion movements. In task 1.2 the investigators aim to investigate how the lesions of patients alter our ability to decode attempted wrist movements (control vs patients group).
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control group | Placebo comparator | Device: MRI, Device: MEG, Device: EEGControl group of healthy subjects |
| Patients group | Active comparator | Device: EEGPatients group of post-stroke with upper-limb deficits on one side |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (23 listed)
- 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.
Key exclusion criteria (27 listed)
- Subjects with characteristics incompatible with MEG and MRI :
- 1. Claustrophobia.
- 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).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| MRIThe healthy subjects in the control group will perform an MRI head scan, which will be used to construct 3D head models and headcasts. | Device | Control group |
| MEGThe healthy subjects will undergo hpMEG data while wearing 3D-printed headcasts created from high resolution MRI | Device | Control group |
| EEGThe healthy participants will undergo a similar session using EEG recording, using a Polhemus Fastrak system for localization of EEG electrodes and precise co-registration with anatomy and hpMEG data. The patients group will take part in the same EEG recording session. | Device | Control group, Patients group |
Primary outcome
Develop subject-specific generative models
Time frame: 2 years
Movement Onset and Offset Detected During Real and Imagined Wrist Extension/Flexion Movements. Direction of Movement Detected During Real and Imagined Wrist Extension/Flexion Movements. Amplitude of Movement Measured During Real and Imagined Wrist Extension/Flexion Movements. Each of these outcome measures focuses on a specific aspect of the movement, providing all the necessary information to developp subject-specific generative models.
1 secondary outcome
Beta burst characterization.
Time frame: 2 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Jul 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing MRI, MEG and EEG in people with Stroke Sequelae and Motor Imagery, run by Hospices Civils de Lyon at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 23 inclusion and 27 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 28 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Develop subject-specific generative models (time frame: 2 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jul 2026.