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

Recruiting now · Not applicable

Conditions studied: Healthy Volunteer

In brief

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.

Key facts

Study ID

NCT06845176

Run by

Centre Hospitalier Universitaire de Saint Etienne

People needed

33

Starts

2026-03-27

Expected to finish

2027-03-01

Last updated by the study team

2026-04-03

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• IRMIS-Hôpital Nord — Saint-Etienne, France, France (enrolling)

Full record on ClinicalTrials.gov

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