Effect of Pillates on Children With Backpack Syndrome

November 18, 2025 updated by: Riphah International University

Effects of Pilates on Pain and Trunk Muscle Endurance in Children With Backpack Syndrome

This randomized clinical trial focuses on a sample of 139 of children diagnosed with backpack syndrome, assessing both subjective pain levels and objective measures of trunk muscle endurance before and after a structured Pilates intervention. The Pilates regimen is designed to strengthen core muscles, improve flexibility, and promote better posture, all of which are critical for mitigating the adverse effects associated with heavy backpack use.Data will be collected from North Star School Allama Iqbal town,Lahore,Standard Grammar School, Allama iqbal town ,Kips School, Allama iqbal town,Ali School System, Allama Iqbal Town Using standardized pain assessment scales(VAS) and endurance tests(Modified Biering-Sørensen Test), the effect of pilates on pain and trunk endurance will concluded and the data will analysed with spss 23

Study Overview

Status

Recruiting

Conditions

Detailed Description

The research titled "Effects of Pilates on Pain and Trunk Muscle Endurance in Children with Backpack Syndrome" investigates the impact of Pilates exercises on alleviating pain and enhancing trunk muscle endurance in children affected by backpack syndrome. Backpack syndrome refers to musculoskeletal discomfort resulting from improper backpack use, often seen in school-aged children who carry heavy loads, leading to poor posture and potential long-term health issues.

This randomized clinical trial focuses on a sample of 139 of children diagnosed with backpack syndrome, assessing both subjective pain levels and objective measures of trunk muscle endurance before and after a structured Pilates intervention. The Pilates regimen is designed to strengthen core muscles, improve flexibility, and promote better posture, all of which are critical for mitigating the adverse effects associated with heavy backpack use.Data will be collected from North Star School Allama Iqbal town,Lahore,Standard Grammar School, Allama iqbal town ,Kips School, Allama iqbal town,Ali School System, Allama Iqbal Town Using standardized pain assessment scales(VAS) and endurance tests(Modified Biering-Sørensen Test), the effect of pilates on pain and trunk endurance will concluded and the data will analysed with spss 23.

Study Type

Interventional

Enrollment (Estimated)

140

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

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 5400

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Children aged 12-16 years.
  • Being Systemically healthy
  • Being physically active and participating in ordinary assessments(4)
  • Children with musculoskeletal backpain
  • Children with hyper thoracic kyphosis i.e. excessive antero-posterior curvature of the thoracic spine of greater than 40°
  • Children complaining about low back pain

Exclusion Criteria:

  • Children with a history of severe musculoskeletal conditions (e.g., scoliosis, fractures, or surgery).
  • Any neurological disorders or developmental conditions affecting motor function
  • Children with cardiological, metabolic or rheumatic illness
  • Children with no complaints of low back pain and postural instability.

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
Active Comparator: Group A
Interventional group
The exercise program will be performed twice a week for 12 weeks changing the exercises for every four weeks. Pilates exercises will consist of four exercises which are selected from original Pilates plan (month 1: rolling back, one leg stretch, shoulder bridge and the push up; month 2: the hundred, one leg stretch, the leg pull and one leg circle; month 3: roll up, scissors, swimming and one leg stretch) (4)
Active Comparator: Group B
Experimental group
Group B will perform routine physical therapy (RPT) alone. These routine exercises will consist of stretching exercises adding some games, stretching and relaxation exercises at the end. i,e stretching exercises, posture training, and spinal flexibility exercises

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Visual Analouge Scale
Time Frame: 12 weeks
The Visual Analog Scale (VAS) is a tool used to measure subjective characteristics or attitudes that cannot be directly measured, commonly used in pain assessment. The scale is often represented as a horizontal line, typically 10 cm in length, anchored by terms at each end that represent extremes of the sensation being measured
12 weeks
Modified Biering-Sørensen
Time Frame: 12 weeks
The Modified Biering-Sørensen Test is an adaptation of the original Biering-Sørensen test, used to assess endurance in the muscles of the lower back, particularly the lumbar extensor muscles. The test measures how long a person can hold a specific static position, which helps evaluate core strength and endurance.
12 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Muhammad Farooqi, MS-PT, 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.

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 27, 2025

Primary Completion (Estimated)

January 25, 2026

Study Completion (Estimated)

January 30, 2026

Study Registration Dates

First Submitted

November 18, 2025

First Submitted That Met QC Criteria

November 18, 2025

First Posted (Actual)

November 25, 2025

Study Record Updates

Last Update Posted (Actual)

November 25, 2025

Last Update Submitted That Met QC Criteria

November 18, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR&AHS/MUHAMMADFAROOQI

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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