Actively Recruiting

Phase Not Applicable
Age: 19Years - 45Years
All Genders
Healthy Volunteers
ID07021079

Effects of Focal Muscle Vibration as a Countermeasure Against Hypoactivity-induced Neuromuscular Deconditioning

Led by Centre Hospitalier Universitaire de Saint Etienne · Updated on 2026-05-26

42

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Muscle deconditioning, which includes loss of muscle mass and strength, often occurs after long periods of reduced use of the lower limbs. This condition is worsened by reduced neural drive, not just muscle loss, highlighting the importance of treatments that improve neuromuscular function during immobilization. Researchers are evaluating the use of focal muscle vibration (FMV), a non-invasive method that activates muscle spindle afferents and causes brain adaptations, as a potential way to counteract this decline. Participants in this study will be randomly assigned to one of two groups. One group will receive a local vibration countermeasure program targeting the knee extensor muscles using small, portable vibrator devices over 10 days to promote neural adaptations. The other group will not receive this vibration treatment, serving as the control group. This approach aims to prevent or reduce strength loss during a period of unilateral lower limb suspension. Throughout the study, participants will undergo measurements at multiple time points (Days 1, 7, 14, 28, and 33) including isometric and maximum voluntary force, jumping performance, postural balance, neuromuscular fatigue, force-velocity-endurance, voluntary activation level, cortico-spinal and spinal excitability, cortical activation, muscle volume, and blood tests for markers of bone and muscle remodeling as well as thrombotic risk. These assessments will help researchers understand the effects of FMV on neuromuscular function and muscle condition over time.

CONDITIONS

Brief Title

Muscle Vibration as a Countermeasure Against Hypoactivity-induced

Who Can Participate

Age: 19Years - 45Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Men and women
  • Aged 18 to 45 years
  • Body Mass Index (BMI) between 18.5 and 24.9 kg/m²
  • Engage in at least 1.5 hours per week of physical activity such as brisk walking, running, swimming, or cycling
  • Provided informed consent after receiving detailed study information
  • Affiliated with or beneficiaries of a social security system
Not Eligible

You will not qualify if you...

  • Chronic cardiovascular, neuromuscular, bone, metabolic, or inflammatory disorders
  • Personal history or risk factors for thrombosis
  • Use of antidepressant medications
  • Use of neuroactive substances that may alter corticospinal excitability during the study
  • Recent bone or ligament trauma within the past 12 months
  • Inability to perform required physical efforts
  • Recent participation in intense or unusual physical activity or sporting competition within the past month
  • Corticosteroid treatment within the past 3 months
  • Any skin lesions at the planned vibration application site
  • Participation in another interventional medical study simultaneously
  • Pregnant or breastfeeding women
  • Unable to understand the study purpose or provide informed consent
  • Deprived of liberty or under guardianship

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - 10 days

Participants receive focal muscle vibration sessions using small and portable vibrator devices or no intervention if assigned to the control group.

Multiple visits during 10-day treatment period

Follow-up

Duration - Up to 23 days after treatment

Participants undergo assessments to measure neuromuscular function and other outcomes after treatment ends.

Visits on Days 14, 28, and 33

Trial Site Locations

Total: 1 location

1

Centre Hospitalier Universitaire

Saint-Etienne, France, 42055

Actively Recruiting

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Research Team

L

LEONARD FEASSON, PHD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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