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Effect of Whole-Body Vibration on Plasma Sclerostin Level

Effect of Whole-Body Vibration on Plasma Sclerostin Level in Healthy Young Adult Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01310335
Acronym
WBV-SCL
Enrollment
15
Registered
2011-03-08
Start date
2011-04-30
Completion date
2011-04-30
Last updated
2016-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteopenia

Keywords

sclerostin, whole-body vibration

Brief summary

The aim of this study is to investigate effect of whole-body vibration on plasma sclerostin level in healthy young adult women. Fifteen healthy young adult women are planned to include in this study. All cases will be trained on a whole-body vibration (WBV) platform (Power Plate) 5 times a week for one week period. Training duration will be short at the beginning but progressed slowly. The amplitude of vibration will be 2 mm and the frequency of the vibration will be 40 Hz. The subjects will be asked to report negative side effects or adverse reactions in their training diary. Previbration and postvibration (just after, 10.minute and 30.minute) levels of plasma sclerostin will be measured on first, second and fifth day of experiment. Sclerostin levels will be measured by human sclerostin ELISA kit.

Detailed description

Whole-body vibration has a strong osteogenic effect. The cyclic mechanical loading to the bone stimulates the osteocytes. 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. The aim of this study is to investigate effect of whole-body vibration on plasma sclerostin level in healthy young adult women.

Interventions

All cases will be trained on a whole-body vibration (WBV) platform (Power Plate) 5 times a week for one week period.

Sponsors

Bagcilar Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy women, * Women with ages varying between 20 and 40 years * Right-handed women

Exclusion criteria

* Lower extremity problems 1. Orthopedic problems: shortness of legs, congenital anomalies, etc. 2. Joint disease (arthritis, joint prosthesis, etc.) 3. Other painful pathologies in the lower extremities (fractures, tendinitis,bursitis, etc.) 4. Circulation problems in the lower extremities * Dorsolumbar diseases: Vertebral fract, disc hernias, spondylodiskitis, etc. * Systemic disease cases 1. Systemic bone disease: osteoporosis, osteomalacia, Paget's disease 2. Hypertension (\>135 mmHg systolic, \>85 mmHg diastolic) 3. Heart dis.(coronary dis, conduction/rhythm prob, cardiac pacemaker) 4. Infectious diseases 5. Endocrine diseases (Diabetes mellitus etc) * Neurological diseases (CNS problems, peripheral neuropathy) * Menstrual cycle disorders, amenorrhea, lactation, oral contraceptive use * Cases during the ovulatory period (11-16th day of menses) * Obesity (BMI \>30 kg/m2) or low BMI (BMI \<20 kg/m2) * Vertigo * Cognitive function disorders * Women whose blood samples were not taken in the time planned * Women whose blood samples hemolyzed

Design outcomes

Primary

MeasureTime frameDescription
Plasma Sclerostin Level1 monthChange of plasma sclerostin level with whole-body vibration

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026