Actively Recruiting
Comparison of the Efficiency of Schroth Method and Schroth Method Based Virtual Reality Exercises in Individuals With Adolescent Idiopathic Scoliosis
Led by Istanbul University - Cerrahpasa · Updated on 2024-06-24
48
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating treatments for adolescent idiopathic scoliosis (AIS), a three-dimensional spinal deformity with unknown cause. This study evaluates the effects of Schroth-based virtual reality exercises compared to traditional Schroth exercises on spinal and postural parameters in adolescents with AIS. The study aims to improve spinal curvature, trunk rotation, and spinal mobility, addressing challenges in long-term treatment adherence and motivation among young patients. Participants will be randomly assigned to one of three groups: a Schroth exercise group, a Schroth method-based virtual reality group using Nintendo Wii games, or a control group on a waiting list. Both exercise groups will follow a 24-week program with supervised sessions twice a week for 12 weeks, then once a week for 12 weeks, totaling 36 sessions. The virtual reality program includes warm-up, balance and sports games, and cool-down, with progression by difficulty and positioning. Control participants will continue usual activities without intervention. Participants will be assessed at baseline, 12 weeks, and 24 weeks for spinal parameters, trunk rotation, spinal mobility, muscle strength, endurance, proprioception, posture symmetry, deformity perception, quality of life, and satisfaction. Researchers will monitor adherence via home exercise reporting during sessions. The study measures outcomes to compare the two exercise methods and understand their impact on scoliosis management in adolescents.
CONDITIONS
Brief Title
Comparison of the Efficiency of Schroth Method and Virtual Reality Exercises in Individuals With AIS
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with adolescent idiopathic scoliosis by an orthopedic specialist
- Aged between 10 and 15 years
- Risser stage between 0 and 3
- Cobb angle between 10 and 30 degrees on anteroposterior radiograph
- Major curvature located in the lumbar region
- No pulmonary or rib cage diseases such as rib fracture, atelectasis, or asthma
- Ability to understand and follow instructions
- Volunteering to participate in the study
You will not qualify if you...
- Using a brace
- Received any scoliosis treatment or spine surgery within the last year
- Any contraindications to exercise
- Neuromuscular, orthopedic, or rheumatic diseases, vestibular problems, vision-related diseases, or mental health issues affecting balance
- Engaged in other exercises or physical activities that affect trunk muscle strength or balance
- Any problem affecting walking other than scoliosis
- Inability to understand and follow instructions
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 24 weeks
Participants receive either Schroth exercises or Schroth method-based virtual reality exercises supervised by a physiotherapist, or continue their routine physical activities if assigned to the control group. Exercise sessions occur 2 days a week for 12 weeks and 1 day a week for the next 12 weeks, totaling 36 sessions over 24 weeks. Home exercises are also included on non-session days.
Up to 36 supervised exercise sessions over 24 weeks
Duration - 24 weeks concurrent with treatment
Participants undergo evaluations of spinal parameters, trunk rotation, spinal mobility, proprioception, muscle strength and endurance, posture symmetry, deformity perception, quality of life, and satisfaction at baseline, 12 weeks, and 24 weeks.
3 assessment visits (baseline, 12 weeks, 24 weeks)
Trial Site Locations
Total: 1 location
1
İrem Kurt
Istanbul, Turkey (Türkiye), 34147
Actively Recruiting
Research Team
İ
İrem KURT ULUSOY, PhD(C)
İ
İpek YELDAN
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here