Comparison of the Effects of Controlled Schroth Exercise and Home Exercise Programs

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

37 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-08-18

Study Completion Date

2021-05-30

Brief Summary

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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

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Detailed Description

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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.

Conditions

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Scoliosis Idiopathic Scoliosis; Adolescence

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Schroth Exercise Group

12 week , Exercises 1 hour, 2 times for a week with physiotherapist 20 minutes home exercise

Group Type EXPERIMENTAL

Schroth Exercise Group

Intervention Type OTHER

12 week , Exercises 1 hour, 2 times for a week with physiotherapist 20 minutes home exercise

Home Exercise Group

Home exercise 20 min at home Once, one hour to determine the Schroth program + teaching home exercises 20 minutes home exercise

Group Type EXPERIMENTAL

Home Exercise Group

Intervention Type OTHER

Home exercise 20 min at home Once, one hour to determine the Schroth program + teaching home exercises 20 minutes home exercise

Interventions

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Schroth Exercise Group

12 week , Exercises 1 hour, 2 times for a week with physiotherapist 20 minutes home exercise

Intervention Type OTHER

Home Exercise Group

Home exercise 20 min at home Once, one hour to determine the Schroth program + teaching home exercises 20 minutes home exercise

Intervention Type OTHER

Eligibility Criteria

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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

Minimum Eligible Age

10 Years

Maximum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes