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Chronic Effects of Tendon Vibrations on the Neuromechanical Muscular Properties. (NEUROVIB)

C

Centre Hospitalier Universitaire de Saint Etienne

Status

Completed

Conditions

Healthy

Treatments

Other: Usual activities
Device: Vibrasens

Study type

Interventional

Funder types

Other

Identifiers

NCT02668224
1408208
2015-A00036-43 (Other Identifier)

Details and patient eligibility

About

It is a randomized, controlled clinical trial, in healthy volunteers. They are in two groups : the test one will perform the vibration training (1h of Vibrasens 3 times a week, 24 sessions) whereas the control group will not be training. The primary outcome is the maximal voluntary strength.

Full description

These last 10 years, a new idea born: vibrations could have potential effects on muscular reconditioning. Researchers have previously demonstrated the effects on plantar ankle flexion, with the increase of the strength, on healthy volunteers. Nowadays physicians would like to demonstrate the effects on another muscular group: ankle's dorsal flexors. 24 sessions are programmed on 8 weeks.

Moreover, the last results showed a modification of the nervous capacities of the cortical voluntary activation. Transcranial Magnetic Stimulation (TMS) is a great tool to explore the neuromuscular function, at the cortical stage. The use of this tool will allow the characterization the effects of the vibration training on the cortical activation state.

Enrollment

46 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Between 18 and 50 years old
  • Both gender
  • Occasional sportsman (<4h/week)
  • Affiliated to a social security scheme
  • Having freely given their written consent

Exclusion criteria

  • Taking neuro-active substances able to modify cortico-spinal excitability from Day 10 to the end of the study
  • Contraindication to magnetic field application
  • Previous pathologies susceptible to modify the process of the tests (particularly stakeholders presenting knee or ankle pathologies)
  • Participation during the same time in another interventional experimentation

Trial design

46 participants in 2 patient groups

Vibrasens : Test group
Experimental group
Description:
Training programme: vibration training 3/week from Day 1 to Day 60 + Usual activities from day 60 to Day 75.
Treatment:
Device: Vibrasens
Control group
Active Comparator group
Description:
Control: Usual activities from day 1 to Day 75.
Treatment:
Other: Usual activities

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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