NCT07424066

Brief Summary

The goal of this interventional cross-sectional study is to evaluate motor responses to non-invasive vibratory stimulation applied to the hamstring muscle tendons in healthy individuals. Knee flexion and extension efforts, in both isometric and concentric contractions, will be tested. The investigators hypothesize that vibratory stimulation causes an increase in activity in the flexor muscles (hamstrings) and a decrease in the extensor muscles (quadriceps) of the knee in all motor tasks. It follows that during knee flexion (both concentric and isometric), vibratory stimulation should cause an increase in the distance between the angular trajectories of the knee obtained with and without vibratory stimulation (with a positive sign). The increased activity of the hamstring muscles would, in fact, contribute to increasing the velocity of the flexor movement. Conversely, during extensor movements (both concentric and isometric), vibratory stimulation should reduce the instantaneous velocity of the movement, therefore causing an increase in distance (with a negative sign) between the trajectories obtained with and without stimulation. Participants will be tested using an isokinetic dynamometer and they will be asked to perform the following motor tasks in a random order: concentric knee flexion, concentric knee extension, isometric knee flexion, and isometric knee extension. The dominant limb will be tested, only. The assessment will be performed one time.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
35

participants targeted

Target at P25-P50 for not_applicable

Timeline
8mo left

Started May 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress60%
May 2025Dec 2026

Study Start

First participant enrolled

May 20, 2025

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

February 6, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

February 20, 2026

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

February 20, 2026

Status Verified

October 1, 2025

Enrollment Period

1.6 years

First QC Date

February 6, 2026

Last Update Submit

February 13, 2026

Conditions

Keywords

vibratory stimulationmuscle spindlemuscle contractionspinal reflexsomatosensory system

Outcome Measures

Primary Outcomes (2)

  • Knee angle

    Maximum distance (in degrees) between the knee trajectory obtained with and without vibratory stimulation.

    Day 1.

  • Surface electromyography (sEMG)

    Difference in sEMG between the muscle activity with and without vibratory stimulation, for each muscle (i.e., Quadriceps, Hamstrings, and Plantarflexor muscles).

    Day 1.

Study Arms (1)

Healthy participants

EXPERIMENTAL

Healthy participants will perform motor tasks with the dominant lower limb, consisting in knee flexion and extension movements in isometric and concentric conditions. The motor tasks will be performed while a vibratory stimulation is applied to hamstring tendons (treatment) and without vibratory stimulation (control) to assess motor responses.

Device: Vibratory stimulation

Interventions

A vibratory stimulator will be applied to the back of the dominant leg, at the level of the hamstring muscle tendons. The stimulator consists of two small vibrating boxes fixed to the leg by means of an elastic band.

Healthy participants

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age equal to or greater than 18 years.

You may not qualify if:

  • Neurological disorders.
  • Musculoskeletal injuries, including previous ones, that may compromise the execution of required movements.
  • Cardiorespiratory disorders.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istituto Auxologico Italiano, Clinica Capitanio

Milan, Milan, 20122, Italy

RECRUITING

Study Officials

  • Cristiano Alessandro, Engineering

    University of Milano Bicocca

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Stefano Scarano, Medical Doctor

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 6, 2026

First Posted

February 20, 2026

Study Start

May 20, 2025

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

February 20, 2026

Record last verified: 2025-10

Locations