RecruitingACTRN12626000407392

Effects of neck muscle vibration on forearm muscle activity in young adults

Vibration-induced modulation of forearm motor unit recruitment and discharge behaviour in healthy young adults


Sponsor

Prof Bernadette Murphy - Ontario Tech University

Enrollment

30 participants

Start Date

Nov 10, 2025

Study Type

Interventional

Conditions

Summary

This study investigates the effects of neck muscle vibration on motor unit activity in forearm muscles of healthy young adults. Participants will complete baseline recordings of forearm muscle activity using high-density surface electromyography (HDsEMG). 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 vibrators are attached but not activated. Following the intervention, HDsEMG recordings will be repeated to assess changes in motor unit recruitment and discharge behaviour. This study aims to determine whether altered proprioceptive input from the neck influences motor unit control in distal upper limb muscles.


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 on a single study visit day, and is not personalized, titrated or adapted across participants. All participants receive identical stimulation parameters within their assigned group. The intervention will be delivered face-to-face on an individual basis in a controlled laboratory environment at a university research facility. The vibration will be applied by trained research personnel with experience in neuromuscular and neurophysiological experimental protocols. Intervention fidelity will be ensured by using identical vibration devices and standardized placement procedures across participants. Adherence is ensured by direct supervision of the intervention by research staff and completion of the full 10-minute vibration or sham period is confirmed for all participants.


Locations(1)

Ontario, Canada

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ACTRN12626000407392