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Clinical Trials/NCT01310335
NCT01310335CompletedNot Applicable

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

Bagcilar Training and Research Hospital1 site in 1 country15 target enrollmentStarted: April 1, 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
15
Locations
1
Primary Endpoint
Plasma Sclerostin Level

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
20 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

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

Exclusion Criteria

  • •Lower extremity problems
  • •Orthopedic problems: shortness of legs, congenital anomalies, etc.
  • •Joint disease (arthritis, joint prosthesis, etc.)
  • •Other painful pathologies in the lower extremities (fractures, tendinitis,bursitis, etc.)
  • •Circulation problems in the lower extremities
  • •Dorsolumbar diseases: Vertebral fract, disc hernias, spondylodiskitis, etc.
  • •Systemic disease cases
  • •Systemic bone disease: osteoporosis, osteomalacia, Paget's disease
  • •Hypertension (>135 mmHg systolic, >85 mmHg diastolic)
  • •Heart dis.(coronary dis, conduction/rhythm prob, cardiac pacemaker)
  • •Infectious diseases
  • •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)
  • •Cognitive function disorders
  • •Women whose blood samples were not taken in the time planned
  • •Women whose blood samples hemolyzed

Arms & Interventions

Training

Experimental

The whole-body vibration (WBV) training

Intervention: whole-body vibration (WBV) (Device)

Outcomes

Primary Outcomes

Plasma Sclerostin Level

Time Frame: 1 month

Change of plasma sclerostin level with whole-body vibration

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Bagcilar Training and Research Hospital
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Ilhan Karacan, Clinical Associated Professor

Chief of Physical Med & Rehab Clinic

Bagcilar Training and Research Hospital

Study Sites (1)

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