Effect of Low Amplitude Vibration Therapy on Flexibility of Hamstring Muscle in Athletes of Pakistan

March 4, 2021 updated by: Dr Jaweria Syed, Shifa Clinical Research Center
Whole body vibration therapy is rapidly becoming a topic of interest for the researchers around the world. Evidence suggests that Whole body vibration has an effect on improving flexibility of hamstring muscle and balance in athletes. The purpose was to examine the effect of low amplitude Whole body vibration on the flexibility of hamstring muscle and improving balance in athletes of Pakistan

Study Overview

Detailed Description

A total 60 number of athletes were analyzed and out of these 40 were included in the study who full fill the inclusion criteria, selected athletes were randomly assigned into two groups (control & experimental). After a total 2 drop outs from control group and 3 drop outs from experimental group, there were 18 athletes in control group and 17 in experimental group who continued till the analysis. Experimental group was given five sessions of low amplitude whole body vibration therapy for almost duration of 10 minutes, on alternative days, along with static stretching of hamstring muscles for 5 minutes and the control group was given only the static hamstring muscle stretches for five minutes, and same five sessions alike on alternative days. Static stretching protocol had 10 stretches in total with 15 seconds stretch time and 30 seconds relaxing time of hamstring muscle. All participants were assessed using Biodex Whole body vibration plate, Biodex balance system , Goniometer and a questionnaire.

Study Type

Interventional

Enrollment (Actual)

40

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

      • Islamabad, Pakistan, 46000
        • Jaweria Syed

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

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • National athletes of Pakistan.
  • Age between 18-30 years

Exclusion Criteria:

  • Athletes having history of any acute injury within last 6 weeks.
  • Athletes who have had any surgical procedure previously or Patients who were medically unstable.

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: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Control group
The control group was given the static hamstring muscle stretches, five sessions on alternative days according to the set protocols.
Static stretching protocol had 10 repetitions in total with 15 seconds stretch time and 30 seconds relaxing time of hamstring muscle.
Pre and post balance assessment by Biodex balance system
Straight Leg Raising to check pre and post Range of Motion by using Goniometer
Experimental: Experimental Group
Given five sessions of low amplitude whole body vibration therapy for duration of 10 minutes, on alternative days, along with static stretching of hamstring muscles.
Pre and post balance assessment by Biodex balance system
Straight Leg Raising to check pre and post Range of Motion by using Goniometer

Given five sessions of low amplitude whole body vibration therapy for duration of 10 minutes, on alternative days, along with static stretching of hamstring muscles.

Static stretching protocol had 10 repetitions in total with 15 seconds stretch time and 30 seconds relaxing time of hamstring muscle.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pre Range of Motion of hamstring muscle (ROM)
Time Frame: outcome at baseline (day zero)
The outcome was the pre status of flexibility in hamstring muscle assessed using Goniometer.
outcome at baseline (day zero)
Post Range of Motion of hamstring muscle (ROM)
Time Frame: outcome at the end of 10 days
The outcome was the post status of flexibility in hamstring muscle assessed using Goniometer.
outcome at the end of 10 days
Pre Balance
Time Frame: outcome at baseline (day zero)
The outcome was pre balance testing using biodex balance system.
outcome at baseline (day zero)
Post Balance
Time Frame: outcome at the end of 10 days
The outcome was post balance testing using biodex balance system.
outcome at the end of 10 days

Collaborators and Investigators

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

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)

August 5, 2017

Primary Completion (Actual)

November 7, 2017

Study Completion (Actual)

January 3, 2018

Study Registration Dates

First Submitted

March 2, 2021

First Submitted That Met QC Criteria

March 4, 2021

First Posted (Actual)

March 5, 2021

Study Record Updates

Last Update Posted (Actual)

March 5, 2021

Last Update Submitted That Met QC Criteria

March 4, 2021

Last Verified

March 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • Riphah/RCRS/REC/00255

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

There is a plan to make IPD and related data dictionaries available

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

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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