RecruitingACTRN12626000408381

Effects of neck muscle vibration on motor planning in healthy young adults

Vibration-induced modulation of movement-related cortical potentials associated with motor planning in healthy young adults


Sponsor

Prof Bernadette Murphy - Ontario Tech University

Enrollment

30 participants

Start Date

Feb 26, 2026

Study Type

Interventional

Conditions

Summary

This study investigates whether neck muscle vibration influences cortical activity associated with motor planning in healthy young adults. Participants will complete baseline electroencephalography (EEG) recordings while performing a voluntary motor task used to measure movement-related cortical potentials (MRCPs). Participants will then receive either 10 minutes of neck muscle vibration applied to the right sternocleidomastoid and left cervical extensor muscles or a sham control condition in which vibratory devices are attached but not activated. EEG recordings will then be repeated to assess changes in MRCPs following the intervention. The study aims to determine whether altered proprioceptive input from neck muscles influences cortical processes involved in movement preparation.


Eligibility

Sex: Both males and femalesMin Age: 17 YearssMax Age: 30 Yearss

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Interventions

The intervention will consist of experimentally induced, high-frequency, low-amplitude mechanical vibration applied to cervical muscles to transiently alter proprioceptive afferent input. Vibration wi

The intervention will consist of experimentally induced, high-frequency, low-amplitude mechanical vibration applied to cervical muscles to transiently alter proprioceptive afferent input. Vibration will be delivered using portable mechanical vibration devices affixed to the skin over the right sternocleidomastoid muscle and left cervical extensor muscles using Hypafix tape. Participants randomly assigned to the active intervention group will receive mechanical vibration at a frequency of 100 Hz with an amplitude of less than 1 mm for a single continuous period of 10 minutes. The intervention will be delivered once during a single laboratory visit following baseline assessments. The intervention will be delivered face-to-face on an individual basis in a controlled laboratory environment at a university research facility by trained research personnel with experience in neuromuscular and neurophysiological experimental protocols. Intervention fidelity will be ensured through the use of identical vibration devices and standardized placement procedures across participants. Adherence will be ensured through direct supervision by research staff, and completion of the full 10-minute stimulation period will be confirmed for all participants.


Locations(1)

Ontario, Canada

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ACTRN12626000408381