Effect of Percussion Massage on Hamstring Flexibility

November 2, 2022 updated by: Pinar Yasar, Suleyman Demirel University

Comparison of Acute Effects of Percussion Massage Therapy and Static Stretching on Hamstring Flexibility

Background and aim: Percussion massage, which is one of the applications to increase muscle flexibility, is a method that combines vibration and massage therapy elements. With its popularity in recent years, it is offered as an alternative to traditional methods that increase flexibility. The aim of this study is to examine the acute effect of percussion massage and static stretching exercise on hamstring flexibility.

Method: Individuals with active knee extension angle limited to at least 15 degree were included in the study, which was designed as a cross-over. Active Knee Extension test and Sit and Reach Test were performed before and after the interventions for the evaluation of hamstring flexibility. Participants were divided into 3 groups as percussion massage, static stretching and control groups, interventions were made with 3 days intervals and control measurements were taken.

Study Overview

Detailed Description

Active knee extansion test: In this test, which is used to evaluate hamstring flexibility in the sitting position, the participant was asked to sit on the edge of the bed and the hip-knee flexion angle was adjusted to 90 degree. For the measurement of active knee extension degree, a double-arm universal goniometer (Baseline Stainless Steel Goniometer; Fabrication Enterprises Inc., Elmsford, NY, USA) was placed on the lateral condyle of the femur and the participant was told to actively extend the knee to full extension. The angle at the end point of the movement was recorded.

sit and reach test: While sitting in a long sitting position with their knees straight and their bodies upright, the participants were asked to touch the soles of their bare feet to the assessment table. In this position, they were told to reach as far as they could reach on the coffee table with their elbows straight and palms facing the floor. By measuring the distance between the fingertip and the coffee table, those who could reach the table received "0" values, those who could reach beyond the table (+) cm and those who could not reach (-) cm. The best value after two measurements was recorded.

Static stretching procedure: For the static stretching exercise, the participant was asked to lie down in the supine position. The investigator had the dominant side passively flexed the hip to 90 degree, extending the knee to the end that could be tolerated. At the last point, it was waited for 30 seconds and then the hamstring muscle was relaxed and rested for 30 seconds. A total of 5 minutes of application was completed by doing 5 repetitions with 30 seconds of static stretching and 30 seconds of rest in each period.

percussion massage procedure: Hypervolt (Hyperice, California, US) device was applied to the dominant hamstring muscle for 5 minutes at 53 Hz frequency with the "hard ball" head. Semitendinosus and semimembranosus muscles were focused in the first 2.5 minutes of the massage treatment, and the biceps femoris muscle in the second 2.5 minutes. By paying attention to the equal amount of pressure applied throughout the massage, the massage was started from the medial side of the muscle in the first part of the application and the massage was completed by moving the device from distal to proximal and from proximal to distal in a straight line within 20 seconds. While passing to the last 2.5 minutes, the massage device was shifted laterally at the distal end of the muscle, and the application was made from distal to proximal and then distally. Thus, the massage for each muscle was started from the medial and ended laterally.

Study Type

Interventional

Enrollment (Actual)

54

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

      • Isparta, Turkey, 32100
        • Faculty of Health Sciences

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

16 years to 23 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

-Active knee extension limited to at least 15 degrees

Exclusion Criteria:

  • Having a hamstring injury in the past two years
  • Having neurological problems in the lower extremity and lumbar region
  • participate in a similar study within the past year

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 Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: control group
no intervention
Active Comparator: percussion massage group
Applying the hypervolt device to the hamstring muscle with the hard ball head for 5 minutes
percussion massage to the dominant leg hamstring muscle for 5 minutes
Other Names:
  • vibration massage
Active Comparator: static stretching group
Static stretching of the hamstring muscle for 5 minutes
Static stretching to the dominant hamstring muscle for 5 minutes

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
knee range of motion measurement
Time Frame: 2 minutes
measurement of maximum knee extension angle in sitting position
2 minutes
hamstring flexibility measurement
Time Frame: 2 minutes
Evaluation of the flexibility of the hamstring muscle in the long sitting position
2 minutes

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Pinar Yasar, MsC, Suleyman Demirel University

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)

February 1, 2022

Primary Completion (Actual)

May 31, 2022

Study Completion (Actual)

May 31, 2022

Study Registration Dates

First Submitted

October 27, 2022

First Submitted That Met QC Criteria

November 2, 2022

First Posted (Actual)

November 7, 2022

Study Record Updates

Last Update Posted (Actual)

November 7, 2022

Last Update Submitted That Met QC Criteria

November 2, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 72867572-050.01.04-31

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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