Effects of Vibration Clinical Trial
Official title:
Effect of Bone Mineral Density on Vibration-Induced Muscle Strength Gain at The Lower Limbs
The aim of this study is to investigate whether there is a relation between bone mineral
density of lower limbs exposed to vibration and the muscle strength gain in the knee
extensors and flexors, and a relation serum sclerostin level and the muscle strength gain in
the knee extensors and flexors in healthy young adult women.
Forty healthy young adult women are planned to include in this study. The participants
meeting the criteria were randomized into two groups: the training group (20 cases) and the
Control group (20 cases).
The whole-body vibration (WBV) training group will be trained on a WBV platform (Power
Plate) 5 times a week for 4 weeks period. Participants will be asked to stand upright on WBV
platform. Training volume and training intensity will be low at the beginning but progressed
slowly according to the overload principle. The training volume will be increased
systematically over the 4-week training period. The training intensity will be increased by
increasing the amplitude (2-4 mm) and the frequency (40 Hz) of the vibration. The subjects
will be asked to report negative side effects or adverse reactions in their training diary.
In the Control group, sham stimulus will be performed by WBV platform 5 times a week for a 4
weeks period.
Plasma sclerostin level and, the right and left knee flexor and extensor muscles strength
will be measured before and after training period. Isokinetic torque will be measured with
the Biodex (Biodex System 3 PRO Multijoint System Biodex Medical Inc. Shirley/NY
USA)extremity-testing system. The right and left lower limbs bone mineral density (BMD) and
muscle strength will be measured before training period. The BMD will be evaluated by bone
densitometer (Norland XR-46 DXA, USA). Sclerostin levels will be measured by human
sclerostin ELISA kit.
The rest muscle electrical activity of right and left knee flexor and extensor muscles will
be evaluated at pre-vibration, post- vibration and, during vibration. The rest muscle
electrical activity will be measured by Powerlab (data acquisition system, ADInstruments,
Australia) device.
Vibration has a strong osteogenic effect. Vibration-induced bone formation is neuronally
regulated. Vibration can also effectively enhance muscle strength and power. Previous
studies have shown that vibration increases muscle electromyographic (EMG) activity.
Attempts to explain vibration-induced increases in EMG activity were based on the tonic
vibration reflex. Tonic vibration reflex activates the muscle spindles, thereby enhancing
the excitatory drive reflex of the alpha motoneurons. On the contrary, it was shown that the
vibration treatment did not enhance the muscle spindle sensitivity and led to presynaptic
inhibition of muscle spindle group Ia afferents. As an alternative to tonic vibration
reflex, the recently described bone myoregulation reflex has been suggested to potentially
explain the increased muscle strength and electrical activity induced by vibration. Based on
the bone myoregulation reflex, bone is sensitive to mechanical stimuli and can send
mechanical input signals to central nervous system and so can neuronally regulate the muscle
activity.
The cyclic mechanical loading to the bone stimulates the osteocytes. According to bone
myoregulation reflex, the more the osteocytes are stimulated by the cyclic mechanical
loading, the increase occurring in the muscle strength and activity may be more. The rate of
osteocytes stimulated by vibration may be determined with serum sclerostin level.
Sclerostin, the protein product of the SOST gene, is an osteocyte-specific cysteine
knot-secreted glycoprotein that is a potent inhibitor of bone formation. Sost/sclerostin
levels have been reported to be reduced by mechanical stimulation.
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Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Basic Science
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