Effects of IASTM vs. Foam Rolling on Knee and Hip Range of Motion in Soccer Players

October 25, 2023 updated by: Riphah International University

Effects of Instrument Assisted Soft Tissue Mobilization vs. Foam Rolling on Knee and Hip Flexibility and Performance in Soccer Players

The aim of this study is:

To compare the acute and long-term affects of instrument assisted soft tissue mobilization (IASTM) vs foam rolling on knee and hip flexibility and performance in soccer players.

Study Overview

Status

Recruiting

Conditions

Detailed Description

The objective of this study is to compare the acute and long-term affects of instrument assisted soft tissue mobilization vs foam rolling on knee and hip flexibility and performance in soccer players. This is a randomized controlled trial, in which participants will be randomly divided into two groups: group-A and group-B. Group-A will receive intervention IASTM while Group-B will receive foam rolling as intervention. Intervention will be carried out for 8 weeks. Assessment of the range of motions for hip and knee joints will be carried out at baseline, immediately after the session, after four weeks and after five (5) months. The secondary measures of performance used in the study are sit and reach test, 100m sprint speed test, Illinois agility run test.

Study Type

Interventional

Enrollment (Estimated)

10

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 Contact

Study Contact Backup

Study Locations

    • Islamabad Capital Territory
      • Islamabad, Islamabad Capital Territory, Pakistan, 44000
        • Recruiting
        • Riphah International University (RIU)
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Individuals with normal BMI
  • Players with at least one year of playing professional soccer and taking at least three training sessions/matches per week.

Exclusion Criteria:

  • Players with any pathological conditions affecting any of the system.
  • Suffering from recent acute unhealed MSK injury/Trauma.

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
Active Comparator: Group A
IASTM Group
Group-A participants would receive Facial Abrasion Technique (FAT) with an Instrument, FAT-Tool. Treatment sessions will be carried out three times per week for eight weeks after an initial warm-up session. All the sessions will be performed at the same time of day (i.e., between 4-6 pm), to avoid possible confounding circadian effects. The FAT group will receive 2 min application on the quadriceps and hamstring muscles with a FAT-tool Pro Large model, which consists of a handle and 20cm treatment surface. The muscles will be treated in a pre-stretched position, meaning a knee flexion in a supine position for the quadriceps muscle and a hip flexion and knee extension in a side-lying position for the hamstring muscles.
Active Comparator: Group B
Foam Rolling Group
Group-B participants would receive Foam Rolling (FR). Treatment sessions will be carried out three times per week for eight weeks after an initial warm-up session. All the sessions will be performed at the same time of day (i.e., between 4-6 pm) to avoid possible confounding circadian effects. The Foam Roller group will receive 2x1 min of FR on the quadriceps and the hamstrings on the dominant leg with the opposite leg crossed over the dominant one. During each minute the muscle will be rolled out 4-5 times, with a break of 30s in between sets. They will be instructed to utilize short, kneading like movements in one direction and a quick motion in the other direction. A grid foam roller will be utilized with a length of 33cm, diameter of 14 cm and with a hard hollow core, wrapped in ethylene vinyl acetate foam.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knee Range of Motion (ROM)
Time Frame: Baseline, after 8 weeks, and after 5 months
Knee ROM will be measured using universal goniometer.
Baseline, after 8 weeks, and after 5 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knee Flexibility (Active Knee Extension Test)
Time Frame: Baseline, after 8 weeks, and after 5 months
Knee flexibility will be assessed using the Active Knee Extension (AKE) test. Assessment of this test will be carried out through a universal goniometer.
Baseline, after 8 weeks, and after 5 months
Knee Flexibility (Sit and Reach Test)
Time Frame: Baseline, after 8 weeks, and after 5 months
Knee flexibility will also be assessed using the Sit and Reach Test. Assessment of this test will be carried out through an improvised ruler/measuring tape.
Baseline, after 8 weeks, and after 5 months
Sprint Speed
Time Frame: Baseline, after 8 weeks, and after 5 months
Sprint speed will be assessed using the time required to complete 100m Sprint Test.
Baseline, after 8 weeks, and after 5 months
Agility
Time Frame: Baseline, after 8 weeks, and after 5 months
Agility will be measured using the time required to complete the Illinois Agility Run Test (IART).
Baseline, after 8 weeks, and after 5 months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Noman Sadiq, MS-SPT, Riphah International University, Islamabad.

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 15, 2023

Primary Completion (Estimated)

November 30, 2023

Study Completion (Estimated)

January 31, 2024

Study Registration Dates

First Submitted

October 11, 2023

First Submitted That Met QC Criteria

October 25, 2023

First Posted (Actual)

October 26, 2023

Study Record Updates

Last Update Posted (Actual)

October 26, 2023

Last Update Submitted That Met QC Criteria

October 25, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • REC/01616 Mansoor Kh Achakzai

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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