Effects of Foam Rolling Versus Stretching Exercises on Quadriceps, Hamstrings and Calf Muscle Length

January 3, 2022 updated by: Riphah International University

Effects of Foam Rolling Versus Stretching Exercises on Quadriceps, Hamstrings and Calf Muscle Length in University Sport's Students

This project will be Randomized control trial conducted to check the effects of foam rolling and stretching exercises on university sport's students so that we can have best treatment option for duration will be for 6 months, purposive sampling data will be done, subject following eligibility criteria from University of Lahore athlete students , were randomly allocated in two groups via lottery method, baseline assessment will be done, Group A participants were given baseline treatment along with foam rolling effects , Group B participants were given baseline treatment along with stretching exercises, pre or post intervention assessment will done via goniometer and Lower extremity functional scale (LESF)and three sessions per week will be given, data will be analyzed by using SPSS version 25.

Study Overview

Status

Completed

Conditions

Detailed Description

The aim of the current study is to determine the effects of foam rolling versus stretching exercises on quadriceps, hamstrings and muscle length in university sport's students. It will be a Randomized control trial and will be conducted at University of Lahore. Purposive sampling technique will be used to collect data as per inclusion criteria the participant age between 18 to 25 years and male and female healthy participants. A history of cardiovascular or respiratory disease, any history of fractures or surgeries in the lower extremity in the past years will be excluded.

Patients will be randomly allocated into two groups; Group A will be treated with the effects of foam rolling on quadriceps, hamstrings and calf muscles. 5 min cycle ergometry, 6 min foam rolling 3 times for 30sec. Group B will be treated with the effects of stretching exercise on quadriceps, hamstrings and calf muscles. 5 min cycle ergometry, 6 min stretching exercises 3 times for 30sec for three sessions of treatment per week will be given. In both group's pre and post-test measurements of quadriceps, hamstrings and calf muscle length will be assessed through goniometer and Lower Extremity Functional Scale (LEFS) will be assessed to measure initial functions of lower limb. Evaluation will be done before session start and at the end of week. Total session will be given for at least 2 months.

Study Type

Interventional

Enrollment (Actual)

50

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

    • Punjab
      • Lahore, Punjab, Pakistan
        • University of Lahore

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 25 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • The age of participants between 18- 25 years.
  • Both male and female young athletes will be included.
  • Healthy participants involved

Exclusion Criteria:

  • A history of cardiovascular or respiratory disease.
  • Any history of fractures or surgeries in the lower extremity in the past year.
  • Any history of third-degree sprains (e.g., anterior cruciate ligament ruptures), grade II or III muscle strain.
  • Any prescribed medication

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group A
Foam Rolling
Group A will be treated with foam rolling effect on quadriceps, hamstring and calf muscle length. 5 min cycle ergometry, 6 min foam rolling 3 times for 30sec.For three session per week will be given atleast for 2 months.
Active Comparator: Group B
Stretching exercises
Group B will be treated with stretching exercises effect on quadriceps, hamstring and calf muscle length. 5 min cycle ergometry, 6 min foam rolling 3 times for 30sec.For three session per week will be given atleast for 2 months.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lower extremity functional scale (LEFS)
Time Frame: 8th Week
It is a questionnaire containing 20 questions about the person's ability to perform task. The LESF can be used by clinicians as a measure of patient's initial function ongoing progress and outcome, as well as to set functional goals.
8th Week
. Goniometric:
Time Frame: 8th Week
It is an instrument which measures the available range of motion at a joint. To measure lower extremity muscles range of motion i.e. quadriceps, hamstrings and calf muscle length
8th Week

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 30, 2021

Primary Completion (Actual)

December 15, 2021

Study Completion (Actual)

December 30, 2021

Study Registration Dates

First Submitted

August 27, 2021

First Submitted That Met QC Criteria

August 27, 2021

First Posted (Actual)

August 30, 2021

Study Record Updates

Last Update Posted (Actual)

January 4, 2022

Last Update Submitted That Met QC Criteria

January 3, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • REC/Lhr/0407 Nubara

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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