Multi Station Training in Soccer Players Hamstrings Strain (EMPTSPHS)

December 25, 2023 updated by: Riphah International University

Effects of Multi Station Proprioceptive Training in Soccer Players With Hamstrings Strain

The study is a randomized controlled trial. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A & B through sealed envelope method by Non-probability Convenient random sampling technique. Group A will be the wobble board proprioceptive training program lasting for four weeks, while Group B will be administered the multi-station proprioceptive training program lasting for four weeks.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

The objective of the study is to determine the effects of Multi-station Proprioceptive training on hamstring strains in Soccer Players. The study is a randomized controlled trial. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A & B through sealed envelope method by Non-probability Convenient random sampling technique. Group A will be the wobble board proprioceptive training program lasting for four weeks, while Group B will be administered the multi-station proprioceptive training program lasting for four weeks. Outcome measures will be assessed by using NPRS, Sit And Reach Test. Lower Extremity Functional Scale. Proximal Hamstring Injury Questionnaire. Balance Training Tool. The collected data will be analyzed in statistical Package for the social Sciences (SPSS) 25.0 .Parametric ∕non|-parametric tests will be applied after test normality of data

Study Type

Interventional

Enrollment (Estimated)

24

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

  • Name: Amna Shahid
  • Phone Number: +92-3344512823

Study Locations

  • Pakistan
    • Punjab
      • Lahore, Punjab, Pakistan, 54000
        • Recruiting
        • Pakistan Sports Board

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:

  • Male football players (trained - not trained) between 14 and 30 years of age, Players with a history of hamstring strain had reduced SLH scores, Players with a history of right knee injury also had reduced SLHB scores on the injured side

Exclusion Criteria:

  • Children and older adults, Upper body proprioceptive training, Presence of pain in any part of upper limb,lower limb, trunk or body which can interfere in training session

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: wooble board proprioceptive training
The group A will perform the wobble board proprioceptive training program lasting for four weeks. Both the training programs consisted of one-leg and double-leg static and dynamic balance drills
Other: wooble board proprioceptive training
this includes wooble board proprioceptive training twice a day for four weeks
Other Names:
  • wooble board training
Other: multi-station proprioceptive training
this includes multi-station proprioceptive training twice a day for four weeks
Other Names:
  • multi-station training
Experimental: multi-station proprioceptive training
The group B will perform the multi-station proprioceptive training program lasting for four weeks. Both the training programs consisted of one-leg and double-leg static and dynamic balance drills basic exercise single length stance walk, Jumper exercise, resistance exercise
Other: wooble board proprioceptive training
this includes wooble board proprioceptive training twice a day for four weeks
Other Names:
  • wooble board training
Other: multi-station proprioceptive training
this includes multi-station proprioceptive training twice a day for four weeks
Other Names:
  • multi-station training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numeric Pain Rating Scale
Time Frame: pre and 4 weeks post intervention
pain will be measured by Numeric Pain Rating Scale (NPRS)
pre and 4 weeks post intervention
Hamstrings and low back flexibility
Time Frame: pre and post 4 weeks intervention
Sit and Reach test will be used to measure hamstrings and low back flexibility
pre and post 4 weeks intervention
Activities of daily living
Time Frame: pre and post 4 weeks intervention
lower extremity functional scale is used to measure ability to perform activities of daily living
pre and post 4 weeks intervention
Single limb stance excursion distances
Time Frame: pre and post 4 weeks intervention
Y balance test will be used to measure single limb stance excursion distances
pre and post 4 weeks intervention

Collaborators and Investigators

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

Sponsor

Riphah International University

Investigators

  • Principal Investigator: Khalid Abbas, Study Principal Investigator

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)

October 20, 2023

Primary Completion (Estimated)

February 20, 2024

Study Completion (Estimated)

February 20, 2024

Study Registration Dates

First Submitted

December 25, 2023

First Submitted That Met QC Criteria

December 25, 2023

First Posted (Actual)

January 9, 2024

Study Record Updates

Last Update Posted (Actual)

January 9, 2024

Last Update Submitted That Met QC Criteria

December 25, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/RCR&AHS/23/0448

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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