Immediate Effects of Whole Body Vibration on Hemodynamic Response and Fatigue in Normotensive People With Obesity (RT)

March 5, 2019 updated by: Tülay Çevik, Okan University

Immediate Effects of Whole Body Vibration on Hemodynamic Response and Fatigue in Normotensive Patients With Obesity

Whole Body Vibration Therapy (WBVT) has been identified as a useful tool to increase peripheral blood flow. The present study aimed at how dynamic exercises with WBVT immediate effect on hemodynamic response and fatigue parameters in patients with obesity.

Study Overview

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey, 34959
        • Okan University Sports Laboratory

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Individuals between age 18-65 with Body Mass Index (BMI) of >29.9 kg/m2

Exclusion Criteria:

  • Unstable hypertensive patients
  • History of cardiovascular, neurologic, or orthopedic diseases,
  • Presence of knee prosthesis, hip replacement
  • Chronic inflammatory disease,
  • Anti-inflammatory treatment
  • Cognitive impairments
  • Pregnancy.

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: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Active Whole Body Vibration Training
Exercises were taught during the first session, active training was done in the second session, and acute evaluations were made during the third session. Both groups performed the dynamic exercises, under supervision, on the whole body vibration device with 10-second rest intervals. Throughout the WBVT session, the vibration amplitude was set to 2 mm and exercise frequency 30 Hz.
Whole Body Vibration Training (WBVT) method has been used as an alternative to conventional strengthening exercises. In this method, the patient stands on the platform of the WBVT device in a static position or performs dynamic exercises, the mechanical vibration produced by the device is transferred to the body
Other Names:
  • Standard Exercise
Active Comparator: Control Group
The same exercises as the aWBVT group were performed on the vibration platform, with the vibration application turned off
Whole Body Vibration Training (WBVT) method has been used as an alternative to conventional strengthening exercises. In this method, the patient stands on the platform of the WBVT device in a static position or performs dynamic exercises, the mechanical vibration produced by the device is transferred to the body
Other Names:
  • Standard Exercise

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Heart rate
Time Frame: "20 minute"
Heart rate was evaluated from the brachial artery using a sphygmanometer.
"20 minute"
Blood pressure
Time Frame: "20 minute"
Blood pressure was evaluated using a sphygmomanometer.
"20 minute"

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Fatigue
Time Frame: "20 minute"
Borg's Rating of Perceived Exertion Scale. Minimum score: 6 Maximum score: 20 The Borg Rating of Perceived Exertion scale helps estimate activity intensity.
"20 minute"

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Dyspnea
Time Frame: "20 minute"
Modified Borg Dyspnea Scale Minimum score 0: breathing is causing no difficulty Maximum score 10: breathing difficulty is maximal
"20 minute"

Collaborators and Investigators

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

Sponsor

Collaborators

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 (Actual)

November 1, 2018

Primary Completion (Actual)

February 15, 2019

Study Completion (Actual)

February 27, 2019

Study Registration Dates

First Submitted

February 27, 2019

First Submitted That Met QC Criteria

March 5, 2019

First Posted (Actual)

March 6, 2019

Study Record Updates

Last Update Posted (Actual)

March 6, 2019

Last Update Submitted That Met QC Criteria

March 5, 2019

Last Verified

March 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • Okan_University

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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