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Motor CortexMOBETANCT04727944

Evaluation of Motor-Related Beta-Activity in Relation to Naturalistic Movement in Healthy Adult Subjects

A study testing Reach and grasp tasks in healthy participants using MEG technique (Experiment 1) and Reach and grasp tasks in healthy participants using EEG technique (Experiment 2) in people with Motor Cortex and Primary Motor Cortex, run by Hospices Civils de Lyon at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The whole body's voluntary movements are controlled by the brain. One of the brain areas most involved in controlling these voluntary movements is the motor cortex and it is often viewed as the primary 'output' region of the neocortex. Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Motor Cortex, Primary Motor Cortex
What is being tested?
Reach and grasp tasks in healthy participants using MEG technique (Experiment 1) and Reach and grasp tasks in healthy participants using EEG technique (Experiment 2)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
31 participants
Where
1 siteFrance
Study dates
28 Jul 2022to 6 Jan 2025
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 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • For all experiments :
  • Healthy male or female
  • Aged 18-40 years
  • Registered with the French healthcare system
  • Motivated to participate in the study
  • Normal or corrected vision
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  • Right-handed
  • Adequate knowledge of French to be able to follow directions
  • Subjects must have the minimal motor ability necessary to participate in the experiment
  • Subjects must be able to listen and understand the study instructions
  • Subjects must be able to give written informed consent before participation
  • Normal hearing

Who cannot join

  • For all experiments :
  • Subjects with characteristics incompatible with MEG/EEG and MRI :
  • Claustrophobia
  • Psychiatric pathology characterized including Alzheimer's disease, Parkinson's disease, multiple sclerosis (MS), or severe traumatic brain injury
  • Neuropsychological disorders or cognitive impairment including schizophrenia, bipolar disorder, seizures, epilepsy, sleep disorders
  • Regular use of neurodevelopment medicines (antidepressants, neuroleptics)
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  • Subject has a history of skin disease or skin allergies (multiple or severe)
  • Subject working with metals in their professional lives
  • The subject had an MRI 2 weeks prior to experiment 1
  • Implanted material (any dental apparatus containing metal including or root canals or any metallic object, pacemaker, cochlear implanted in the body)
  • Pregnant women or lactating women (based on self-report)
  • subjects who are not able to tolerate sitting for 1 hour (the estimated length of the experiment)
  • Alcohol dependence
  • Subjects who, in the opinion of the investigator are not able or willing to comply with the protocol
  • For experiment 1:
  • A head size incompatible with the use of a personalized 3D head-cast or a magnetoencephalography

Trial locations and contacts

1 site in 1 country.

France1 site
  • Institut des Sciences Cognitives, Marc Jeannerod, UMR 5229 CNRS

    Bron, 69500

Other trials in France

About this study

The whole body's voluntary movements are controlled by the brain. One of the brain areas most involved in controlling these voluntary movements is the motor cortex and it is often viewed as the primary 'output' region of the neocortex. Motor cortical activity in the beta frequency range (13-30Hz) is a hallmark signature of healthy and pathological movement, but its behavioral relevance remains unclear. Such uncertainty confounds the development of treatments for diseases of movement which are associated with pathophysiological beta activity, including Parkinson's, therefore furthering understanding on the behavioral significance of activity in this range is now vital. Recently, it has become apparent that oscillatory beta activity actually occurs in discrete transient bursts, and that the summation of short-lasting, high-powered bursts of activity only appear to be sustained oscillations when averaged over multiple trials.

In this study we will use neurophysiological and neuroimaging techniques such as electroencephalography (EEG), magnetoencephalography (MEG), and magnetic resonance imaging (MRI). All of these techniques have been identified as non-invasive techniques. By applying these methods, we will be able to analyze beta burst activity in order to determine how beta bursts influence naturalistic motor behavior.

Read more

This project also encompasses the study of auditory and motor interactions doing an experimental task.

The aim of the project is to get a better understanding of the role of motor-related beta activity during the preparation and generation of reach and grasp actions. These findings may inform novel treatments for pathophysiological disorders characterized by aberrant beta signaling, utilizing causal manipulation of the neural circuits implicated in the generation of beta activity. This project also has expected methodological repercussions. It will make it possible to validate the use of individualized head-casts worn during MEG acquisition for the study of the cortical control of naturalistic actions, and to create new analysis tools that allow an increase in the spatial resolution of MEG data.

Being tested
Reach and grasp tasks in healthy participants using MEG technique (Experiment 1), Reach and grasp tasks in healthy participants using EEG technique (Experiment 2)
Keywords
Beta burst activity, Naturalistic motor behavior, Neuroimaging techniques, electroencephalography (EEG), magnetoencephalography (MEG), magnetic resonance imaging (MRI), Reach and Grasp

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Reach and grasp tasks in healthy participants using MEG technique (Experiment 1)Other

    Human participants will perform reach and grasp movements to various objects (e.g. a cube, sphere, or rod) driven either by perceived action affordances, or instruction cues. A rotating carousel will be used to present subjects with various objects affording different types of grasps (e.g. a precision pinch, a whole hand 'power' grasp, or a tripod grasp).

    Prior to the experiment, subjects will be tested outside the scanner by asking them to grasp each object as they would naturally to ensure that each object elicits the expected grasp type. Subject-specific, 3D-printed head-casts will be created based on high resolution MRI scans from each subject, and worn by subjects during the MEG experiment (Experiment 1) to reduce within-session head movement associated with reaching and grasping.

    At the end of this session an experimental task is added: detection of tons in presence of multitonal masks, in order to verify how beta peaks might be generated by a stimulus auditory.

  • Reach and grasp tasks in healthy participants using EEG technique (Experiment 2)Other

    Experiment 2 consists of a task of reaching for and grasping several objects (e.g. a cube, sphere, or rod) ; the task used for experiment 2 is the same as that used for experiment 1. EEG signals will be measured.

Study groups in NCT04727944
Study groupRoleWhat they receive
MEG and EEG recordings on Healthy volunteersExperimentalAll subjects can participate in experiment 1 and/or 2. All analyses are intra-subject (no analyses are between-subject). * Experiment 1 will test the functional role of beta bursts in naturalistic action preparation, using a combined anatomical MEG-MRI approach which will be conducted in 2 sessions. * Experiment 2 will study the relationship between beta bursts and naturalistic action preparation using EEG.
Receives: Other: Reach and grasp tasks in healthy participants using MEG technique (Experiment 1); Other: Reach and grasp tasks in healthy participants using EEG technique (Experiment 2)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Timing of beta bursts in motor cortex, measured with MEG before initiation of a movement

    Timing (ms, relative to motion onset) of beta bursts in motor cortex with MEGthan the one planned is cued and must be performed.

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years

  2. Spatial location of beta bursts in motor cortex, measured with MEG before initiation of a movement

    Spatial location (mm, in a brain-centered reference frame) of beta bursts in motor cortex, measured with MEG

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years

  3. Timing of beta bursts in motor cortex, measured with EEG before initiation of a movement

    Timing (ms, relative to motion onset) of beta bursts in motor cortex with EEG

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years

  4. Spatial location of beta bursts in motor cortex, measured with EEG before initiation of a movement

    Spatial location (mm, in a brain-centered reference frame) of beta bursts in motor cortex, measured with EEG

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years

Secondary outcomes (10)
  1. Timing of beta bursts in motor cortex, measured with MEG before initiation of a movement

    Timing (ms, relative to motion onset) of beta bursts in motor cortex with MEG

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years

  2. Spatial location of beta bursts in motor cortex, measured with MEG before initiation of a movement

    Spatial location (mm, in a brain-centered reference frame) of beta bursts in motor cortex, measured with MEG

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years

  3. Timing of beta bursts in motor cortex, measured with EEG before initiation of a movement

    Timing (ms, relative to motion onset) of beta bursts in motor cortex with EEG

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years

  4. Spatial location of beta bursts in motor cortex, measured with EEG before initiation of a movement

    Spatial location (mm, in a brain-centered reference frame) of beta bursts in motor cortex, measured with EEG

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years

  5. Beta amplitude, measured with MEG

    Beta amplitude (fT) in motor cortex, measured with MEG

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years

  6. Beta amplitude, measured with EEG

    Beta amplitude (μV) in motor cortex, measured with EEG

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years

  7. Determine what aspects of grasp kinematics can be decoded from beta burst activity in motor cortex and related regions.

    Multivariate machine learning models which are able to predict the trajectory of arm and hand kinematics from the spatiotemporal pattern of beta bursts in motor cortex.

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years.

  8. Within-session movement

    Movement (mm) of fiducial locations of the head-cast relative to the MEG sensors

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years.

  9. Visual stimuli

    Comparison of synchronization, localization and waveform of beta peaks in the motor cortex in response ovisual stimuli.

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years.

  10. Auditory stimuli

    Comparison of synchronization, localization and waveform of beta peaks in the motor cortex in response to auditory stimuli.

    Measured: The data of subjects will be collected and analyzed through study completion an average of 2 years.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Jan 2021
  2. Study start28 Jul 2022
  3. Primary completion6 Jan 2025
  4. Study completion6 Jan 2025

Resources

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
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
31 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04727944
Sponsor's protocol ID
69HCL20_0843
Other IDs
2021-A00042-39
Acronym
MOBETA
Status last verified
Aug 2025
First submitted
18 Jan 2021
Last updated
14 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Reach and grasp tasks in healthy participants using MEG technique (Experiment 1) and Reach and grasp tasks in healthy participants using EEG technique (Experiment 2) in people with Motor Cortex and Primary Motor Cortex, 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 12 inclusion and 16 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 14 Aug 2025. 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. 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?

Timing of beta bursts in motor cortex, measured with MEG before initiation of a movement (time frame: The data of subjects will be collected and analyzed through study completion an average of 2 years). The study lists 4 primary outcomes in all. 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 14 Aug 2025.

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