Effects of Whole-Body Vibration on Balance in the Elderly Population

December 19, 2014 updated by: Slavko Rogan, cand. PhD, PTMsc, Bern University of Applied Sciences

Effects of Stochastic Resonance Therapy on Postural Control in the Elderly Population (Pilot Study)

The goal of this pilot study is to test whether in the elderly population there are acute long-term improvements in both the static and dynamic balance, reaction time and mobility with the use of WBV.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Exercise therapy plays an important role in health promotion, preservation of physical function and in preventing loss of independence among the elderly. They work beside an improvement in balance, a positive effect on metabolic and cardiovascular disorders, reducing falls, osteoporosis, colon cancer, breast cancer, depression, anxiety, and the general well-being. There is preliminary evidence to indicated that balance, and strength can be trained in the elderly using whole-body vibration (WBV) therapy. The use of WBV in the elderly population has shown to be a simple and effective treatment in the areas of balance and mobility. It would be very desirable to investigate these factors further in order to provide evidence for the delivery of sustainability of training methods.

Study Type

Interventional

Enrollment (Actual)

20

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years to 95 years (OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • BESA to include performance level 0,1,2.
  • live in the senior residence Multengut Muri or in the canton of Bern.
  • apart from the complaints of old age healthy and can stand with or without aids.
  • more than 22 points at the Mini-Mental State Examination

Exclusion Criteria:

  • Seniors / graduates may no severe, uncorrected visual disturbances (eg, low vision, double vision, skew deviation).
  • Acute stress the incompatibility of the lower limb / hip / ridge during the SRT: joint disease, thrombosis, fresh fractures, infections, tissue damage, or fresh surgical scars.
  • Seniors / inside with lower leg-/thigh prostheses.
  • alcoholics.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: CROSSOVER
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Group 1
T0, Stochastic resonance whole-body vibration A intervention over four weeks, three time a week;T1, 16 days wash-out period; T2, Stochastic resonance whole-body vibration B intervention over four weeks, three times week, T3
Device: Stochastic resonance whole-body vibration A
over four weeks, three times a week with 5 Hz, Noise 4 and than over four weeks three times a week with 1 Hz, Noise 1.
Other Names:
  • Zeptor med ®
Device: Stochastic resonance whole-body vibration b
over four weeks, three times a week with 1 Hz, Noise 1 and than four weeks three times a week with 5 Hz, Noise 4.
Other Names:
  • Zeptor med ®
EXPERIMENTAL: Group 2
T0, Stochastic resonance whole-body vibration B intervention over four weeks, three time a week;T1, 16 days wash-out period;T2, Stochastic resonance whole-body vibration A intervention over four weeks, three times week, T3
Device: Stochastic resonance whole-body vibration A
over four weeks, three times a week with 5 Hz, Noise 4 and than over four weeks three times a week with 1 Hz, Noise 1.
Other Names:
  • Zeptor med ®
Device: Stochastic resonance whole-body vibration b
over four weeks, three times a week with 1 Hz, Noise 1 and than four weeks three times a week with 5 Hz, Noise 4.
Other Names:
  • Zeptor med ®

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
static balance
Time Frame: after one session, four and eight weeks
after one session, four and eight weeks

Secondary Outcome Measures

Outcome Measure
Time Frame
reaction time
Time Frame: after one session, after four and eight weeks
after one session, after four and eight weeks
dynamic balance
Time Frame: after one session, four and eight weeks
after one session, four and eight weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Bern University of Applied Sciences

Collaborators

Goethe University
Maastricht University Medical Center
Swiss Federal Institute of Technology

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2010

Primary Completion (ACTUAL)

September 1, 2010

Study Completion (ACTUAL)

September 1, 2010

Study Registration Dates

First Submitted

January 8, 2010

First Submitted That Met QC Criteria

January 8, 2010

First Posted (ESTIMATE)

January 11, 2010

Study Record Updates

Last Update Posted (ESTIMATE)

December 23, 2014

Last Update Submitted That Met QC Criteria

December 19, 2014

Last Verified

December 1, 2014

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • PhD pilot study I

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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