Actively Recruiting
Resisted Inspiratory Muscle Training Applied in Addition to PSSE-Schroth Exercises
Led by Hacettepe University · Updated on 2026-03-03
45
Participants Needed
1
Research Sites
60 weeks
Total Duration
On this page
Sponsors
H
Hacettepe University
Lead Sponsor
K
Kirsehir Ahi Evran Universitesi
Collaborating Sponsor
AI-Summary
What this Trial Is About
This prospective randomized controlled trial will evaluate whether adding resisted inspiratory muscle training (IMT) to Physiotherapeutic Scoliosis-Specific Exercises (PSSE)-Schroth exercises provides additional benefits on clinical outcomes in individuals with adolescent idiopathic scoliosis. Participants will be randomly assigned to either PSSE-Schroth plus IMT or PSSE-Schroth alone. Both groups will receive supervised exercise sessions three times per week for 8 weeks (24 sessions). Outcomes will be assessed before and after the intervention and will include clinical measures (e.g., Cobb angle, angle of trunk rotation, Posterior Trunk Symmetry Index, The Walter Reed Visual Assessment Scale), respiratory muscle performance (maximal inspiratory pressure/maximal expiratory pressure, six-minute walk test) and related physiological parameters, functional performance (balance, 3D kinematics, plantar pressure analysis, isokinetic strength), sleep quality, and health-related quality of life (Scoliosis Research Society- 22, Italian Spine Youth Quality of Life). The study is expected to enroll approximately 45 participants.
CONDITIONS
Official Title
Resisted Inspiratory Muscle Training Applied in Addition to PSSE-Schroth Exercises
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female adolescents aged 10 to 18 years
- Diagnosis of adolescent idiopathic scoliosis
- Cobb angle between 106 and 456
- Angle trunk rotation (ATR) 25 56
- Risser 24 3 and Sanders 24 4
- No scoliosis-related procedure within the last 6 months
- No contraindication to exercise
You will not qualify if you...
- Non-idiopathic scoliosis (neuromuscular, congenital, syndromic)
- Inability to achieve 2580% adherence/compliance
- History of spinal surgery or major trauma
- Cardiopulmonary diseases contraindicating exercise
- Neurological, rheumatological, vestibular, or systemic diseases
- Acute musculoskeletal injury or impaired skin integrity
- Participation in a regular PSSE-Schroth or IMT program within the last 3 months
- Intellectual disability or communication difficulties preventing protocol adherence
- Newly initiated brace treatment or high risk of non-compliance with brace management
- Lack of informed consent
AI-Screening
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Trial Site Locations
Total: 1 location
1
Kırşehir Ahi Evran University
Kırşehir, Merkez, Turkey (Türkiye), 40100
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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