Actively Recruiting
Schroth and Scapular Muscle Activation in Hyperkyphosis
Led by Istanbul University - Cerrahpasa · Updated on 2025-10-01
56
Participants Needed
1
Research Sites
58 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This randomized controlled trial aims to investigate the effects of Schroth exercises on scapular muscle activation in children with thoracic hyperkyphosis. A total of 56 participants will be randomly assigned to either the Schroth exercise group or the control group receiving postural education. The intervention group will complete an 8-week supervised Schroth program focusing on three-dimensional correction, rotational breathing, and postural awareness. Primary outcome is scapular muscle activation measured by surface EMG. Secondary outcomes include muscle strength, scapular endurance, kyphotic appearance, posture, and pain. The results will guide clinical management and preventive strategies for children with postural thoracic hyperkyphosis.
CONDITIONS
Official Title
Schroth and Scapular Muscle Activation in Hyperkyphosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Thoracic kyphosis angle (Cobb) between �3e40�b0 and <70�b0 on lateral radiographs
- Aged 7-18 years
- Risser stage 0-5, indicating ongoing skeletal development
You will not qualify if you...
- Congenital or rigid spinal deformities/anomalies
- Major musculoskeletal surgery or trauma, especially involving the spine
- Physiotherapeutic intervention for the spine in the last 6 months
- Current brace use
- BMI �3e= 30
- Regular upper extremity sports involvement (e.g., swimming, volleyball) at least twice a week for one year
- More than 60 minutes of moderate-to-high intensity physical activity per week
- Visual impairments or light sensitivity
- Positive vestibular (Unterberger) test
- Hearing impairments
- Cognitive difficulties affecting comprehension
- Systemic diseases (diabetes, hypothyroidism, infection, malignancy)
- Neurological disorders
- Active rheumatic diseases
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Istanbul University-Cerrahpasa
Istanbul, Istanbul, Turkey (Türkiye)
Actively Recruiting
Research Team
K
Kübra Kardeş, PhD
CONTACT
T
Turgut Akgül, Prof
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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