- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07638826
Mat-Pilates Exercises on Balance in Adolescents With Scoliosis
June 5, 2026 updated by: Eman Wagdy, Beni-Suef University
Efficacy of Mat-Pilates Exercises on Balance and Functional Capacity in Adolescents With Scoliosis. A Randomized Controlled Trial.
The aim of this study is to examine the effects of mat-Pilates exercises on balance and functional capacity in adolescents with scoliosis.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Adolescent scoliosis is one of the common spinal deformities observed during adolescence period aged between 10-16 years.
It can introduce wide-ranging dysfunction in different bodily systems and organs.
Numerous researchers present that standing balance assessments show greater postural instability in adolescent with scoliosis compared with age-matched controls.
Pilates exercises emphasizes the development of a neutral spine as it consists of stretching, strengthening, and coordination activities.
Consequently, it could improve the stability of the spine, muscle strength, and flexibility of the pelvis, and hip joints that in turn, could improve balance, lower limbs strength, and functional capacity.
Several studies support the use of mat-Pilates exercises among different areas in adults while, there is no research conducted on balance and functional capacity in children and adolescents with scoliosis.
Hence, there is need to study the efficacy of mat-Pilates exercises on balance and functional capacity in adolescents with scoliosis.
Study Type
Interventional
Enrollment (Estimated)
40
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
- Name: Eman Wagdy, PH.D
- Phone Number: 01008079576
- Email: Eman.wagdy@pt.bsu.edu.eg
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
No
Description
Inclusion Criteria:
- Adolescents ages will be ranged from 12 to 15 years old.
- Cobb's angles ranging from 10° to 25°.
- Functional Hearing and vision.
- Independent standing and walking.
Exclusion Criteria:
- Either spine, upper, or lower limbs fractures.
- Leg length discrepancy or foot deformities.
- Rheumatic and congenital heart disease.
- History of previous surgical operation.
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Conventional Physical Therapy
Adolescents with scoliosis will receive the conventional physical therapy for 45 min./session
|
It includes stretching exercises of the concave side muscles, strengthening exercises of the convex side muscles, postural control exercises from sitting and standing, and breathing exercises.
|
|
Experimental: Mat-Pilates
Adolescents with scoliosis will receive the conventional physical therapy for 45 minutes/session in addition to mat-pilates exercises for 45 min./session
|
It includes stretching exercises of the concave side muscles, strengthening exercises of the convex side muscles, postural control exercises from sitting and standing, and breathing exercises.
It includes a selected pilates exercises in the form of bridge, hundred, alternate toe taps, single leg circles, side to side, side kick lying, quadruped, spine twist, side leg raise, and tandem walking
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance
Time Frame: Up to 12 weeks
|
Biodex Stability System will be used to measure overall stability index, anteroposterior stability index and mediolateral stability index.
|
Up to 12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional Capacity
Time Frame: Up to 12 weeks
|
Six-minute walk test will be used for measuring functional capacity.
It is a sub-maximal test of aerobic capacity, in which the subjects walk as far as possible in 6 minutes (min.)
around a premeasured distance.
|
Up to 12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
June 15, 2026
Primary Completion (Estimated)
September 15, 2026
Study Completion (Estimated)
September 15, 2026
Study Registration Dates
First Submitted
June 5, 2026
First Submitted That Met QC Criteria
June 5, 2026
First Posted (Actual)
June 10, 2026
Study Record Updates
Last Update Posted (Actual)
June 10, 2026
Last Update Submitted That Met QC Criteria
June 5, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- P.T.REC/012/006462
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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