The Effect of Schroth Method on Pain, Body Awareness and Quality of Life in Adolescent Individuals With Idiopathic Scoliosis

Hacettepe University40 enrolled

Overview

This study was aimed to compare the effect of Schroth therapy method, which is a 3-dimensional scoliosis exercise method, and traditional exercises on pain, body awareness and quality of life in young individuals with idiopathic scoliosis.

38 individuals aged between 10-18 with the diagnosis of idiopathic scoliosis will be participated in the study. Individuals (study group) underwent 1 hour exercise program 3 times a week for 6 weeks, and the individuals (control group) undervent a traditional exercise program once a week under supervision of physiotherapist for 6 weeks. During the rest of the week, same exercise program was given as a home program for at least half an hour a day and individuals will followed up. Individuals' subjective pain intensity will be assessed with Visual Analogue Scale (VAS), pressure pain threshold by algometer, body awareness by Turkish version of Body Awareness Questionnaire and quality of life by Turkish version of Scoliosis Research Society (SRS)-22 scale. Measurements will be performed before and after the 6-week exercise program.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Scoliosis

Interventions

exercise programme 1OTHER

Schroth three dimensional scoliosis therapy method

exercise programme 2OTHER

Traditional scoliosis exercises

Eligibility

Sex: ALLMin age: 10 YearsMax age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Having been diagnosed with idiopathic scoliosis by a specialist physician, * Between the ages of 10-18, * Primary curvature between 20-40 degrees according to the Cobb method, * Having C or S type of scoliosis, * Having back / low-back pain due to scoliosis, * Those who have not received any previous exercise therapy for scoliosis, * Volunteering to participate in the study, * Having the cognitive capacity to cooperate with the directions of the physiotherapist, * Has not suffered any injuries to the musculoskeletal system in the last 6 months, * No neurological, orthopedic or cardiopulmonary disorders other than scoliosis diagnosis, * Young individuals who have not undergone any surgery related to the diagnosis of scoliosis Exclusion Criteria: * Previous spinal surgery, * Any disease other than idiopathic scoliosis, * Individuals who cannot adapt to the directions of the physiotherapist and cannot fulfill the requirements of the exercise program

Locations (1)

Fizyo Omurga

Konya, Turkey (Türkiye)

Outcomes

Primary Outcomes

Pain Level

Pain level will be assessed with VAS (visual analog scale) (min:0, max:10)

Time frame: 6 weeks

Pressure Pain Threshold

Pressure pain threshold with algometer (kg/cm\^2).

Time frame: 6 weeks

Secondary Outcomes

Body awareness before and after treatment

body awareness assessment will be done with body awareness questionnaire (min:18, max:126 pts.)

Time frame: 6 weeks

Data from ClinicalTrials.gov

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