Actively Recruiting
Non-invasive Vibratory Stimulation of the Knee Muscles for the Improvement of the Somatosensory Input and Motor Performance
Led by University of Milano Bicocca · Updated on 2026-02-20
35
Participants Needed
1
Research Sites
84 weeks
Total Duration
On this page
Sponsors
U
University of Milano Bicocca
Lead Sponsor
I
Istituto Auxologico Italiano
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Non-invasive Vibratory Stimulation of the Knee Muscles for the Improvement of the Somatosensory Input and Motor Performance
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age equal to or greater than 18 years.
You will not qualify if you...
- Neurological disorders.
- Musculoskeletal injuries, including previous ones, that may compromise the execution of required movements.
- Cardiorespiratory disorders.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Istituto Auxologico Italiano, Clinica Capitanio
Milan, Milan, Italy, 20122
Actively Recruiting
Research Team
S
Stefano Scarano, Medical Doctor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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