Effect of Scoliosis and Progressive Resistance Exercises on Clinical and Pulmonary Parameters in Adolescents With Idiopathic Scoliosis
SPRE-AIS
Effects of Scoliosis Exercises and Upper and Lower Extremity Progressive Resistance Exercises on Anthropometric, Clinical, and Pulmonary Parameters in Adolescents With Idiopathic Scoliosis
1 other identifier
interventional
24
1 country
1
Brief Summary
Adolescent idiopathic scoliosis (AIS) is a common spinal deformity that may affect physical function and pulmonary capacity during adolescence. Exercise-based rehabilitation programs are frequently used in the conservative management of scoliosis. The aim of this study is to investigate the effects of scoliosis-specific exercises combined with upper and lower extremity progressive resistance exercises on anthropometric, clinical, and pulmonary parameters in adolescents with idiopathic scoliosis. Participants diagnosed with adolescent idiopathic scoliosis will participate in an exercise program including scoliosis-specific exercises and progressive resistance exercises targeting upper and lower extremities. Anthropometric measurements, clinical assessments, and pulmonary function parameters will be evaluated before and after the intervention. The results of this study are expected to provide evidence regarding the effectiveness of combined exercise interventions on physical and respiratory outcomes in adolescents with idiopathic scoliosis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 30, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 30, 2026
CompletedFirst Submitted
Initial submission to the registry
March 15, 2026
CompletedFirst Posted
Study publicly available on registry
March 18, 2026
CompletedMarch 18, 2026
March 1, 2026
8 months
March 15, 2026
March 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Muscle Thickness Measured by Ultrasonography
Changes in diaphragm, lumbar multifidus and pectoralis major muscle thickness measured by ultrasonography.
Baseline and after 4 weeks of exercise intervention
Secondary Outcomes (4)
Sit and Reach Flexibility Test
Baseline and after 4 weeks of intervention
Back Scratch Test
Baseline and after 4 weeks of intervention
Hand Grip Strength
Baseline and after 4 weeks of intervention
Pulmonary Function Test
Baseline and after 4 weeks of intervention
Study Arms (2)
Scoliosis Exercise Program
EXPERIMENTALParticipants perform scoliosis-specific exercises designed to improve spinal alignment, posture, and respiratory function.
Progressive Resistance Exercise Program
EXPERIMENTALParticipants perform upper and lower extremity progressive resistance exercises targeting major muscle groups.
Interventions
Scoliosis-specific exercise program designed to improve spinal alignment, posture, and respiratory function in adolescents with idiopathic scoliosis. The program includes supervised therapeutic exercises performed under physiotherapist guidance.
Progressive resistance exercise program targeting upper and lower extremity muscle groups including biceps, triceps, pectoral, back, quadriceps, and hamstring muscles.
Eligibility Criteria
You may qualify if:
- Adolescents aged between 12 and 18 years diagnosed with adolescent idiopathic scoliosis (AIS)
- Cobb angle between 10° and 25° confirmed by radiological evaluation
- C-type scoliosis curve pattern
You may not qualify if:
- Presence of congenital scoliosis
- Presence of chromosomal abnormalities
- Presence of skeletal dysplasia
- Presence of connective tissue disease
- Presence of neuromuscular disease
- Presence of metabolic diseases affecting bone metabolism
- Calcium metabolism disorders
- Severe autoimmune diseases
- Severe endocrine diseases
- Severe cognitive impairment
- Orthopedic conditions preventing participation in exercise
- History of spinal surgery
- History of excisional procedure or surgery involving paravertebral muscles
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ankara Bilkent City Hospital
Ankara, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Researcher
Study Record Dates
First Submitted
March 15, 2026
First Posted
March 18, 2026
Study Start
June 1, 2025
Primary Completion
January 30, 2026
Study Completion
January 30, 2026
Last Updated
March 18, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share