RecruitingNot ApplicableNCT07021079

Muscle Vibration as a Countermeasure Against Hypoactivity-induced

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


Sponsor

Centre Hospitalier Universitaire de Saint Etienne

Enrollment

42 participants

Start Date

Jun 16, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Muscle deconditioning, characterized by a loss of muscle mass and strength, is a frequent consequence of prolonged lower limb unloading. Beyond muscle mass loss, reduced neural drive contributes significantly to strength decline, highlighting the need for interventions targeting neuromuscular function during immobilization. Focal muscle vibration (FMV) has shown promise in modulating neuromuscular excitability by activating muscle spindle afferents and inducing cortical adaptations. Chronic use of FMV has been associated with significant strength gains and improved neural command. This makes FMV an effective rehabilitation tool. Its simplicity and non-invasiveness further make it a practical countermeasure.


Eligibility

Min Age: 19 YearsMax Age: 45 Years

Inclusion Criteria6

  • Men and women.
  • Aged 18 to 45 years.
  • Body Mass Index (BMI) between 20 and 25 kg/m².
  • Engaging in at least 1.5 hours per week of physical activity (e.g., brisk walking, running, swimming, cycling).
  • Provided informed consent after receiving detailed information about the study.
  • Affiliated with or beneficiaries of a social security system

Exclusion Criteria13

  • Chronic cardiovascular, neuromuscular, bone, metabolic, and/or inflammatory disorders.
  • Personal history and/or risk factors for thrombosis.
  • Use of antidepressant medications.
  • Use of neuroactive substances likely to alter corticospinal excitability (e.g., hypnotics, antiepileptics, psychotropics, muscle relaxants) during the study.
  • Recent bone or ligament trauma within the past 12 months.
  • Inability to perform the physical efforts required for the study.
  • Recent participation in a sporting competition or intense, unusual physical activity within the past month.
  • Corticosteroid treatment within the past 3 months.
  • Any skin lesions at the planned vibrator application site.
  • Simultaneous participation in another interventional medical study.
  • Pregnant or breastfeeding women.
  • Individuals unable to understand the purpose and conditions of the study or unable to provide informed consent.
  • Individuals deprived of liberty or under guardianship

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Interventions

DEVICEFocal muscle vibration

focal muscle vibration sessions, using small and portable vibrator devices.

DEVICENO Focal muscle vibration

The control group will not receive any intervention.


Locations(1)

Centre Hospitalier Universitaire

Saint-Etienne, France

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NCT07021079


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