The Effects of Combining Whole Body Vibration Training With Plyometric Jumping on the Neuromuscular Adaptations of Human Triceps Surae Muscles

January 20, 2011 updated by: National Taiwan University Hospital
Muscle force, explosive strength and vertical jump height are important parameters determining the performance of athletes. Traditionally, high intensity resistance training, explosive strength training and plyometric training are used to improve athletes' performance. Recently, whole body vibration training is recommended for increasing muscle force and explosive strength, because vibrating platform could provide high gravitational acceleration to activate muscle activation and sensory input to spinal reflex. Design: Prospective and randomized control study. Subjects: Healthy male subjects with regular training or competition at least 6 hours per week. Methods: H-reflex, V-wave, triceps surae activation level and rate of force development are measured at pre-training, mid-training (5th week) and post-training. Subjects will receive 8 weeks, 3 times/week, training programs including plyometric jumping or static squat on whole body vibration platform. Data analysis: Data will be analyzed using SPSS 13.0 software (SPSS Inc., Chicago, IL) and two-way ANOVA will be used for data analysis.

Study Overview

Status

Unknown

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

30

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

      • Taipei, Taiwan, 100
        • Recruiting
        • National Taiwan University
        • Contact:
        • Principal Investigator:
          • HK Wang, PhD

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 30 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • subjects who had not been engaged in systematic strength training and had no history of knee, leg, or ankle pain that caused a subject to seek medical help during the year prior to the recruitment.

Exclusion Criteria:

  • Subjects who missed more than one training session or participated in any other type of fitness training were excluded.

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

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: No vibration
Active Comparator: vibration
8 week vibration

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
evoked spinal reflex
Time Frame: 8 weeks
In terms of evoked spinal reflexes, modulations of spinal inhibitory inter-neuronal circuits are often assessed by the Ia-afferent-mediated H-reflex. Results of H reflexes in studies with training are tightly coupled with excitability changes of small alpha motor neurons. The first volitional (V) wave, an electrophysiological variant of the H-reflex, is used to indicate the net excitation of the motorneurone pool.
8 weeks

Collaborators and Investigators

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

Investigators

  • Study Chair: Hsing-Kuo Wang, PhD, National Taiwan University Hospital

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, 2011

Primary Completion (Anticipated)

November 1, 2011

Study Completion (Anticipated)

December 1, 2011

Study Registration Dates

First Submitted

January 20, 2011

First Submitted That Met QC Criteria

January 20, 2011

First Posted (Estimate)

January 24, 2011

Study Record Updates

Last Update Posted (Estimate)

January 24, 2011

Last Update Submitted That Met QC Criteria

January 20, 2011

Last Verified

January 1, 2011

More Information

Terms related to this study

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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