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Clinical Trials/NCT04203394
NCT04203394
Completed
Not Applicable

Comparison of the Effects of Controlled Schroth Exercise and Home Programs on Body Symmetry, Deformity Perception and Quality of Life in Adolescent Idiopathic Scoliosis

Eastern Mediterranean University1 site in 1 country37 target enrollmentAugust 18, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Scoliosis Idiopathic
Sponsor
Eastern Mediterranean University
Enrollment
37
Locations
1
Primary Endpoint
3D Motion analysis
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The aim of this study is to compare the effects of Schroth 3D exercise method on home symmetry, trunk topography, scapula symmetry, pelvic symmetry, health related quality of life and cosmetic deformity perception in adolescents with idiopathic scoliosis

Detailed Description

Cobb angle measurement, which is accepted as the gold standard in patients with scoliosis, is a radiological measurement. However, in continuous follow-up, the search for other methods to obtain objective data that will provide a short term evaluation on the patient in determining the efficacy of conservative treatment continues. In our study, individuals who meet the criteria will be evaluated at the beginning and end of the study. Sociodemographic features and scoliosis characteristics (Cobb angle, degree of bone maturation according to Risser, apex, vertebra rotation angle) will be recorded. Posterior Trunk Asymmetry Index (POTSI) will be used to determine body asymmetry, and topographic measurements will be performed with Artec Eva 3D Scanner and motion analysis will be performed with Biomechanical Motion Analysis Sistem (Model is BTS Smart DX100) . Individuals will evaluate their cosmetic deformities with the Walter Reed Visual Evaluation Scale. Scoliosis Research Society-22 will be used to measure quality of life.

Registry
clinicaltrials.gov
Start Date
August 18, 2019
End Date
May 30, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with scoliosis diagnosed and followed up by the attending physician
  • 10-16 age group,
  • Patients who voluntarily agreed to participate in the study
  • Living in Antalya/TURKEY

Exclusion Criteria

  • Mental retardation, congenital scoliosis or spinal deformity, spinal surgery, neuromuscular disease, rheumatologic disease, tumor, cardiovascular or pulmonary disease, vertigo attack or balance problem, neurological disease
  • İndividual who does not sign the consent form

Outcomes

Primary Outcomes

3D Motion analysis

Time Frame: 12 weeks

3D motion analysis with 4 cameras, symmetry of certain points will be evaluated during motion.

Postural Trunk Asymmetry Index (POTSI)

Time Frame: 12 weeks

It is a method that allows an individual with AIS to evaluate body shape and asymmetry.

Root Mean Square(RMS)

Time Frame: 12 weeks

Body right and left asymmetry will be examined.

Walter Reed Visuel Assesment Scale

Time Frame: 12 weeks

Walter Reed Visuel Assesment Scale (WRVAS) each aspect is shown with five levels of increasing severity of the seven type of deformity that are scored from minimum (1) to maximum (5). How individuals perceive their own cosmetic deformities and the effectiveness of treatment in improving cosmetic deformity can be evaluated

Scoliosis Research Society-22

Time Frame: 12 weeks

Scoliosis Research Society (SRS-22) is a simple and practical questionnaire specific to individuals with scoliosis. The questionnaire included pain, self-image, function / activity, mental health and treatment satisfaction. There are 22 questionnaire questions, scoring from 1 to 5. The minimum score is the worst score (22).

Study Sites (1)

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