Effects of Movement Pattern Training Versus Proprioceptive Neuromuscular Training in Footballers With Groin Pain

February 10, 2025 updated by: Riphah International University

Effects of Movement Pattern Training Versus Proprioceptive Neuromuscular Training on Pain Range of Motion Flexibility and Kick Distance in Footballers With Groin Pain

Effects Of Movement Pattern Training Versus Proprioceptive Neuromuscular Facilitation On Pain Range Of Motion Flexibility and Kick Distance Among Footballers With Groin Pain.

Study Overview

Detailed Description

According to the literature, due to the small number of PT studies on elite athletes (compared with the number of studies on general athletes), it is necessary to further understand whether PT can also benefit this group and accurately test the sports science equipment to facilitate the planning of accurate training courses.There is limited number of studies that have investigated comparative effects of pattern training and propiocetive neuro muscular facilitation..Also, there was no study found that Effects Of Movement Pattern Training Versus Proprioceptive Neuromuscular Facilitation On Pain Range Of Motion Flexibility and Kick Distance Among Footballers With Groin Pain.

Study Type

Interventional

Enrollment (Estimated)

36

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

      • Lahore, Pakistan
        • Pakistan Sports Academy

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • History of groin or adductor strain Patient Neurological involvement that influenced coordination or balance
  • Male players,groin pain during or after the game
  • groin pain > 8 weeks.
  • Tenderness on palpation.
  • pain during hip adduction with resistance
  • Willingness to participate in the research

Exclusion Criteria:

  • Subjects with urinary tract infection
  • Lower limb fractures,
  • metastasis
  • Spinal pathology,
  • hip joint osteoarthritis
  • Inguinal pain(2).

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: Movement Pattern Training
The group A Comprises 18 participants and will perform Movement Pattern Training 2set each set 20 repition lasting for eight weeks.
The group A Movement Pattern Training 2set each set 20 repition lasting for eight weeks.
Experimental: propioceptive neuromuscular facilitation
The group B Comprises 18 participants and will perform propioceptive neuromuscular facilitation 2set each set 20 repition lasting for eight weeks.
The group B propioceptive neuromuscular facilitation 2set each set 20 repition lasting for eight weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
International Hip Outcome Tool
Time Frame: 8 weeks
Overall iHOT-33 and iHOT-12 scores were calculated as the mean visual analog scale score for the individual items for each questionnaire for each patient)
8 weeks
Sit And Reach Flexibility Test.
Time Frame: 8 weeks
The sit and reach test is a common measure of flexibility, and specifically measures the flexibility of the lower back and hamstring muscles.sit and reach box (or alternatively a ruler can be used, and a step or box)
8 weeks
Hip Rotation (Goniometer)
Time Frame: 8 weeks
Hip Internal and External Rotation Range of motions will be measured
8 weeks
Kicking For Distance
Time Frame: 8 weeks
Measuring Tapes will be used to measure the kick distance
8 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Awais ul Mustafa, DPT, Riphah International University

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)

April 24, 2024

Primary Completion (Estimated)

February 10, 2025

Study Completion (Estimated)

February 15, 2025

Study Registration Dates

First Submitted

November 18, 2024

First Submitted That Met QC Criteria

February 10, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 10, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR&AHS/24/0403

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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