- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07248514
Effect of Pillates on Children With Backpack Syndrome
Effects of Pilates on Pain and Trunk Muscle Endurance in Children With Backpack Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: IMRAN AMJAD, PhD
- Phone Number: 9233224390125
- Email: imran.amjad@riphah.edu.pk
Study Contact Backup
- Name: Muhammad Asif Javed, MS-PT
- Phone Number: 923224209422
- Email: a.javed@riphah.edu.pk
Study Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 5400
- Recruiting
- Imran Amjad
-
Contact:
- Muhmmad Asif Javed, MS
- Phone Number: 033224209422
- Email: a.javed@ripah.edu.pk
-
Contact:
- Muhammad Farooqi, MS-PT
- Phone Number: 03367129899
- Email: m.faruki97@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
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
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
Sponsor
Investigators
- Principal Investigator: Muhammad Farooqi, MS-PT, Riphah International University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS/MUHAMMADFAROOQI
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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