Combining Motor Imagery and Tendon Vibration on the Effectiveness of Motor Imagery

NCT ID: NCT06845176

Last Updated: 2025-02-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

33 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-03-11

Study Completion Date

2027-03-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Kinesthetic motor imagery (kMI) involves imagining the sensations of movement, activating brain regions similar to actual movement execution. It is widely used to maintain or restore motor functions, particularly in rehabilitation. Tendon vibration (TV), which stimulates proprioceptive receptors can also enhance corticospinal excitability and promote neuroplasticity. This project investigates the coupling of kMI and TV through three modalities: simultaneous application, TV application between kMI trials, or pre-application of TV to precondition the nervous system before kMI trials. The effectiveness and quality of kMI will be assessed by corticospinal excitability measurements using transcranial magnetic stimulation and EEG measures. Conducting this study in healthy participants will inform the development of optimized clinical interventions for immobilized or mobility-reduced patients.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Healthy Volunteer

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Simultaneous application of TV and kMI

Simultaneous application of Tendon Vibration and Kinesthesic Motor Imagery

Group Type EXPERIMENTAL

Tendon vibration (TV)

Intervention Type DEVICE

We use the VIBRAMOOV PHYSIO device which delivers local muscle vibrations at frequencies of 80 Hz and an amplitude of 1 mm.

Kinesthetic motor imagery (kMI)

Intervention Type OTHER

kMI is a mental technique in which an individual visualizes performing a movement without physically executing it. This process involves the internal representation of the sensations associated with the movement, engaging neural pathways similar to those activated during actual physical movement. kMI stimulates key motor and sensory areas in the brain, promoting neuroplasticity and enhancing motor performance.

TV application between kMI trials

Tendon Vibration application between Kinesthesic Motor Imagery

Group Type EXPERIMENTAL

Tendon vibration (TV)

Intervention Type DEVICE

We use the VIBRAMOOV PHYSIO device which delivers local muscle vibrations at frequencies of 80 Hz and an amplitude of 1 mm.

Kinesthetic motor imagery (kMI)

Intervention Type OTHER

kMI is a mental technique in which an individual visualizes performing a movement without physically executing it. This process involves the internal representation of the sensations associated with the movement, engaging neural pathways similar to those activated during actual physical movement. kMI stimulates key motor and sensory areas in the brain, promoting neuroplasticity and enhancing motor performance.

TV as a pre-conditionning for kMI

Tendon Vibration application as a pre-conditionning for Kinesthesic Motor Imagery

Group Type EXPERIMENTAL

Tendon vibration (TV)

Intervention Type DEVICE

We use the VIBRAMOOV PHYSIO device which delivers local muscle vibrations at frequencies of 80 Hz and an amplitude of 1 mm.

Kinesthetic motor imagery (kMI)

Intervention Type OTHER

kMI is a mental technique in which an individual visualizes performing a movement without physically executing it. This process involves the internal representation of the sensations associated with the movement, engaging neural pathways similar to those activated during actual physical movement. kMI stimulates key motor and sensory areas in the brain, promoting neuroplasticity and enhancing motor performance.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Tendon vibration (TV)

We use the VIBRAMOOV PHYSIO device which delivers local muscle vibrations at frequencies of 80 Hz and an amplitude of 1 mm.

Intervention Type DEVICE

Kinesthetic motor imagery (kMI)

kMI is a mental technique in which an individual visualizes performing a movement without physically executing it. This process involves the internal representation of the sensations associated with the movement, engaging neural pathways similar to those activated during actual physical movement. kMI stimulates key motor and sensory areas in the brain, promoting neuroplasticity and enhancing motor performance.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Men or women aged 18 to 50 years.
* Affiliated with or beneficiaries of a social security system.
* Provided written informed consent freely after being informed of the study's purpose, procedures, and potential risks.

Exclusion Criteria

* History of pathology or surgery affecting upper limb motor function within 6 months prior to the study.
* Chronic neurological, motor, or psychiatric disorders.
* Use of neuroactive substances likely to alter corticospinal excitability (e.g., hypnotics, antiepileptics, psychotropics, muscle relaxants) during the study period.
* Contraindications to transcranial magnetic stimulation
* Simultaneous participation in another interventional study or participation in such a study within 30 days prior to this study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Jean Monnet University

OTHER

Sponsor Role collaborator

Centre Hospitalier Universitaire de Saint Etienne

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Léonard FEASSON, PhD

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universiatire de SAINT-ETIENNE

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

IRMIS-Hôpital Nord

Saint-Etienne, France, France

Site Status

Countries

Review the countries where the study has at least one active or historical site.

France

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Léonard FEASSON, PhD

Role: CONTACT

04 77 12 03 83 ext. 33

Diana RIMAUD, Doctor of Science

Role: CONTACT

0477120467 ext. 33

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Diana RIMAUD, Docor of science

Role: primary

0477120467 ext. 33

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2024-A02856-41

Identifier Type: OTHER

Identifier Source: secondary_id

24CH250

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.