Acute Effect of Instrument-Assisted Soft Tissue Mobilization on Hamstring Flexibility Via Fascial Chain

September 11, 2023 updated by: Erkan Erol, Tokat Gaziosmanpasa University
Instrument assisted soft tissue mobilization (IASTM) is one of the methods used to achieve fascial release. In this study, it will be examined whether there will be an increase in hamstring flexibility by releasing the superficial posterior fascial chain as a result of the IASTM technique to be applied over the triceps surae muscle and plantar fascia. Sociodemographic information of individuals who meet the inclusion criteria and volunteer to participate in the study will be obtained, and straight leg lift test and popliteal angle measurement will be performed with the digital inclinometer (Baseline Digital Inclinometer) to be provided within the scope of the project to measure hamstring flexibility. Then, IASTM will be applied to the triceps surae muscle and plantar fascia for 15 minutes. Measurements will be repeated after the application.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

35

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

      • Tokat, Turkey, 60250
        • Faculty of Health Sciences, Tokat Gaziosmanpaşa University

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

Description

Inclusion Criteria:

  • Healthy individuals with a straight leg lift test less than 80° and a popliteal angle greater than 15° will be included in the study.

Exclusion Criteria:

  • Individuals with a history of lower extremity fractures, lumbar disc herniation, acute pain, a history of lesion in the hamstring muscles at least 1 month before the study, knee or hip prosthesis, and those using drugs that may affect the measurements (e.g., muscle relaxants) will not be included in the study.

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: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Instrument Assisted Soft Tissue Mobilization Group
With the IASTM device, application will be made over the skin to the triceps surae muscle and plantar fascia for 15 minutes. The application will be made in the prone position. Massage oil will be used to reduce tissue friction before the application.
With the IASTM device, application will be made over the skin to the triceps surae muscle and plantar fascia for 15 minutes. The application will be made in the prone position. Massage oil will be used to reduce tissue friction before the application.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Straight Leg Raise Test
Time Frame: Baseline
Measurements will be made with a digital inclinometer. In the supine position, the digital inclinometer will be inserted into the tuberositas tibia. Then, the participant's leg will be passively lifted by the researcher with the knee extended. The leg will be brought to the point where the tension is felt, where the value on the inclinometer will be recorded. It will then return to the starting position. The procedure will be repeated for both legs.
Baseline
Straight Leg Raise Test
Time Frame: 1 hour
Measurements will be made with a digital inclinometer. In the supine position, the digital inclinometer will be inserted into the tuberositas tibia. Then, the participant's leg will be passively lifted by the researcher with the knee extended. The leg will be brought to the point where the tension is felt, where the value on the inclinometer will be recorded. It will then return to the starting position. The procedure will be repeated for both legs.
1 hour
Popliteal angle test
Time Frame: Baseline
In the supine position, the hip and knee will be brought to 90 degrees. The digital inclinometer will be placed on the tuberositas tibia and the participant will be asked to extend the knee while maintaining the position of the hip. At the last point, the value on the inclinometer will be recorded. It will then return to the starting position. The procedure will be repeated for both legs.
Baseline
Popliteal angle test
Time Frame: 1 hour
In the supine position, the hip and knee will be brought to 90 degrees. The digital inclinometer will be placed on the tuberositas tibia and the participant will be asked to extend the knee while maintaining the position of the hip. At the last point, the value on the inclinometer will be recorded. It will then return to the starting position. The procedure will be repeated for both legs.
1 hour

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)

March 30, 2023

Primary Completion (Actual)

May 31, 2023

Study Completion (Actual)

June 30, 2023

Study Registration Dates

First Submitted

February 19, 2023

First Submitted That Met QC Criteria

February 28, 2023

First Posted (Actual)

March 1, 2023

Study Record Updates

Last Update Posted (Actual)

September 13, 2023

Last Update Submitted That Met QC Criteria

September 11, 2023

Last Verified

September 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • GaziosmanpasaU_Erol_06

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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