Release Versus Post Isometric Relaxation Among Futsal Players With Shin Splints

June 26, 2023 updated by: Riphah International University

Effects of Myofascial Release Versus Post Isometric Relaxation Among Futsal Players With Shin Splints

The aim of the study is to determine the effects of myofascial release versus post isometric relaxation among futsal players with shin splints

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Previous literature did not compare the combined effects of both myofascial release and post isometric relaxation technique inn sgin splints patients so the purpose of this study is self-explanatory, with the basic goal of comparing these two techniques to determine their effects on patient Pain, and Functional disability thus improving overall performance of the futsal players.This study will be helpful in proposing proper treatment for shin splint, to make people aware of the condition rehabilitation and improving performance of the futsal players undergoing the condition. Thus it will be useful for the betterment of the players overall health and wellbeing.

Study Type

Interventional

Enrollment (Estimated)

32

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 Locations

  • Pakistan
    • Punjab
      • Lahore, Punjab, Pakistan
        • Recruiting
        • Model town hospital

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:

  • Subjects have leg pain with exertion of more than 1 or 2 hours
  • Participants age 20-30 years
  • Participants have MTSS for more than 2 weeks
  • Subjects have No previous history of trauma to legs
  • Subject having Local pain on lower anterior leg Gradual cessation of the offending activity

Exclusion Criteria:

  • • Subjects have medical history of systemic disease

    • Subjects have Medical history of cardiovascular disease
    • Participants with History of metastatic diseases
    • Any trauma or pathology of lower limb Participants having Neuropathy of lower extremity

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
Myofascial release
Other: Myofscual release
I will apply myofascial release on group A patients and observse its effects on shin splint
Other Names:
  • Hot pack
Experimental: Group B
Post isometric relaxation
Other: Post isometric relaxation.
I will apply post isonetric relaxation on group b patients and observe effects on shin splint
Other Names:
  • Hot pack

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numeric pain rating scale
Time Frame: 3 months
Numeric pain rating scale NPRS is a subjective measure in which Pain intensity is frequently measured on an 11-point pain intensity scale (PI-NRS), where 0=no pain and 10=worst possible pain.
3 months
Lower extremity functional scale
Time Frame: 3 months
Lower extremity functional scale LEFS is a valid, reliable, and responsive tool that can be used to measure function in patients with lower extremity musculoskeletal dysfunction
3 months

Collaborators and Investigators

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

Sponsor

Riphah International University

Investigators

  • Principal Investigator: Nosheen Manzoor, Riphah International 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)

November 22, 2022

Primary Completion (Estimated)

July 15, 2023

Study Completion (Estimated)

July 25, 2023

Study Registration Dates

First Submitted

June 26, 2023

First Submitted That Met QC Criteria

June 26, 2023

First Posted (Actual)

July 5, 2023

Study Record Updates

Last Update Posted (Actual)

July 5, 2023

Last Update Submitted That Met QC Criteria

June 26, 2023

Last Verified

June 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/RCR & AHS/23/0425

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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