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Three-Dimensional Scoliosis Exercises and Diaphragmatic Manual Techniques in Adolescents With Idiopathic Scoliosis

1 luglio 2026 aggiornato da: Neriman Temel Aksu, Akdeniz University

The Effectiveness of Three-Dimensional Scoliosis Exercises Supported by Diaphragmatic Manual Techniques in Adolescents With Idiopathic Scoliosis: A Randomized Controlled Study

Adolescent idiopathic scoliosis (AIS) is a three-dimensional deformity of the spine that emerges during growth and is characterized by lateral curvature, vertebral rotation, and trunk asymmetry. AIS can negatively affect not only the spinal structure but also postural control, trunk stability, muscle activation patterns, respiratory function, and the quality of life of individuals. Particularly in thoracic curvatures, decreased rib cage mobility and impaired functional effectiveness of the diaphragm and intercostal muscles can lead to reduced respiratory capacity and respiratory muscle strength. Therefore, in scoliosis rehabilitation, it is important to evaluate not only spinal alignment but also respiratory mechanics and diaphragmatic function. Currently, among conservative treatment approaches, Three-Dimensional Scoliosis Exercises (Schroth method) are widely used and reported to be effective in reducing curvature progression. However, scientific evidence regarding the effects of supporting Schroth exercises with diaphragmatic manual techniques on muscle activation, trunk derotation, and respiratory function is limited. Since the diaphragm is both a primary respiratory muscle and an important postural muscle involved in spinal stabilization, it is thought that improving diaphragmatic function may contribute to scoliosis rehabilitation. In this randomized controlled trial, 24 individuals aged 10-18 years diagnosed with AIS will be divided into two groups. The study group will receive Schroth exercises supported by diaphragmatic manual techniques, while the control group will receive only Schroth exercises. Participants will be evaluated before and after treatment in terms of superficial muscle activity, Cobb angle, trunk rotation angle, perception of cosmetic deformity, respiratory functions, respiratory muscle strength, and quality of life. The unique value of this research is that it is one of the limited number of studies that multidimensionally examine the effects of diaphragmatic manual techniques combined with Schroth exercises on electromyographic muscle activation, derotation, and respiratory functions. It is expected that the results will contribute to the development of new rehabilitation approaches in the conservative treatment of AIS, strengthen evidence-based physiotherapy practices, and improve the quality of life of individuals with scoliosis.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Adolescent idiopathic scoliosis is characterized by a three-dimensional deformity of the spine and can cause changes in muscle strength, muscle activation, trunk stability, and respiratory function. Considering the role of the diaphragm muscle in postural control and spinal stabilization, it is thought that disorders in diaphragmatic function may contribute to scoliosis progression. Three-dimensional scoliosis exercises (Schroth exercises), with their three-dimensional correction principles and rotational breathing techniques, are frequently used in scoliosis rehabilitation. However, the effects of supplementing Schroth exercises with diaphragmatic manual techniques on muscle activation and trunk derotation have not been sufficiently clarified. The results of this study are expected to contribute to determining the effectiveness of breath-based manual approaches in scoliosis rehabilitation and to provide a scientific basis for physiotherapy applications. Although there are studies in the literature examining the effects of Schroth exercises on curvature angle, posture, and quality of life, studies investigating the effects of applying diaphragmatic manual techniques in conjunction with Schroth exercises on electromyographic muscle activation and derotation are limited. Adolescent idiopathic scoliosis is a progressive musculoskeletal problem that emerges during the growth period and is characterized by a three-dimensional deformity of the spine. Lateral curvature, vertebral rotation, and trunk asymmetry in the spine can negatively affect individuals' postural control, respiratory functions, and muscle activation patterns. In recent years, three-dimensional scoliosis exercises and brace therapy have become widely used among conservative treatment methods, and these approaches have been reported to be effective in reducing curvature progression. However, the effects of diaphragmatic manual techniques on respiratory mechanics, trunk stabilization, and muscle activation, and the results of their combined use with three-dimensional scoliosis exercises, have not yet been sufficiently investigated. This study aims to investigate the effects of diaphragmatic manual techniques and 3D scoliosis exercises, applied for 12 weeks, on superficial muscle activity, scoliosis severity, trunk rotation angle, perception of cosmetic deformity, respiratory function, respiratory muscle strength, and quality of life in individuals with adolescent idiopathic scoliosis.

Although there are studies in the literature examining the effects of 3D scoliosis exercises on curvature angle, posture, and quality of life, studies evaluating the effects of applying diaphragmatic manual techniques in conjunction with 3D scoliosis exercises on EMG activation, scoliosis severity, trunk rotation angle, perception of cosmetic deformity, respiratory function, respiratory muscle strength, and quality of life are limited. Therefore, the aim of this research is to contribute to the development of new rehabilitation approaches in the conservative treatment of adolescent idiopathic scoliosis.This study aims to investigate the effects of diaphragmatic manual techniques and 3D scoliosis exercises, applied for 12 weeks, on superficial muscle activity, scoliosis severity, trunk rotation angle, perception of cosmetic deformity, respiratory function, respiratory muscle strength, and quality of life in individuals with adolescent idiopathic scoliosis. Although there are studies in the literature examining the effects of 3D scoliosis exercises on curvature angle, posture, and quality of life, studies evaluating the effects of applying diaphragmatic manual techniques in conjunction with 3D scoliosis exercises on EMG activation, scoliosis severity, trunk rotation angle, perception of cosmetic deformity, respiratory function, respiratory muscle strength, and quality of life are limited. Therefore, the aim of this research is to contribute to the development of new rehabilitation approaches in the conservative treatment of adolescent idiopathic scoliosis.

Tipo di studio

Interventistico

Iscrizione (Stimato)

24

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

  • Nome: Açelya Kocabey
  • Numero di telefono: 05332786187

Luoghi di studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Individuals aged 10-18 years, in adolescence.
  • Scoliosis curvature in the thoracic region.
  • Individuals and their parents (those who have signed the informed consent form) who agree to participate in regular follow-up and exercise programs throughout the study period.
  • Diagnosis of AIS by a physician.
  • Patients with idiopathic scoliosis diagnosed radiologically and with a Cobb angle less than 30°.
  • The child and family agree to participate in and adhere to the 12-week treatment process.
  • Ability to understand and speak Turkish.
  • Not being in another treatment program. Individuals without any systemic disease that prevents participation in the physical exercise program.

Exclusion Criteria:

  • Individuals who report that they cannot participate regularly during the exercise period or who will not adhere to the study schedule.
  • Individuals who have not previously undergone surgery for scoliosis
  • Those with accompanying neuromuscular or rheumatic diseases
  • Those receiving other scoliosis-related treatment during the study
  • Malignancy
  • Those using braces
  • Individuals with cognitive impairment that prevents them from understanding and performing the exercises mentally or physically.
  • Those with respiratory and cardiovascular system diseases requiring regular medication

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Prevenzione
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Diaphragmatic manual techniques and Schroth exercises
The Diaphragmatic manual techniques and Schroth exercises group will receive 15 minutes of diaphragmatic manual techniques followed by 45 minutes of Schroth exercises.
Altro: Diaphragmatic manual techniques
With the patient sitting upright, the physiotherapist will position themselves behind the patient, placing their hands across the rib cage and fingertips to the subcostal margins. As the patient exhales, the physiotherapist will apply gentle but firm lateral pulling force from the subcostal margin to stretch the diaphragm. This pulling will be continued during inhalation. After repeating this for several breathing cycles, the patient will be placed supine, with hands bilaterally placed on the lower ribs, and mobilization will be performed in a figure-eight pattern. For diaphragm mobilization, individuals will lie comfortably on their backs. The physiotherapist, positioned above the individual's head, will place the hypothenar region and the last three fingers of their hands bilaterally on the 7th-10th costal cartilages. The therapist will apply lateral and longitudinal pulls with their hands to support rib elevation during inspiration.
Altro: Schroth exercises
During a Schroth exercise session, the goal is to stabilize proper posture by lengthening shortened muscles and activating stretched muscles through rotational breathing, based on the principles of active elongation, deflection, and derotation postural correction. Individuals will be positioned in three different positions-sleeping, sitting, and standing-with passive or active support, and stabilization will be achieved through isometric stretching. Each position will be held for 10 breaths*3 sets, and the therapist will monitor the corrections throughout the session.
Comparatore attivo: Schroth exercises
Patients in the Schroth exercises group will only perform Schroth exercises for 60 minutes.
Altro: Schroth exercises
During a Schroth exercise session, the goal is to stabilize proper posture by lengthening shortened muscles and activating stretched muscles through rotational breathing, based on the principles of active elongation, deflection, and derotation postural correction. Individuals will be positioned in three different positions-sleeping, sitting, and standing-with passive or active support, and stabilization will be achieved through isometric stretching. Each position will be held for 10 breaths*3 sets, and the therapist will monitor the corrections throughout the session.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change of Ossification of the Iliac Apophysis
Lasso di tempo: Changes from baseline Ossification of the Iliac Apophysis at 12 weeks.

Evaluation of skeletal maturation is necessary to determine the patient's risk of progression. Risser grading is one of the most commonly used methods for measuring ossification of the iliac apophysis.

Stage 0: No ossification

Stage 1: Ossification of up to 25% of the iliac apophysis

Stage 2: Ossification of 25% to 50% of the iliac apophysis

Stage 3: Ossification of 50% to 75% of the iliac apophysis

Stage 4: Ossification of more than 75% of the iliac apophysis

Stage 5: Complete bone fusion of the iliac apophysis

Growth is not considered complete until Stage 5 is reached; therefore, one of the inclusion criteria for the study is a maximum Risser stage of 4.
Changes from baseline Ossification of the Iliac Apophysis at 12 weeks.
Change of Severity of Scoliosis
Lasso di tempo: Change from baseline severity of scoliosis at 12 weeks.
The Cobb angle is an angle method that radiologically measures the degree of curvature. This angle is based on the angle between the top and bottom edges of the spinal segments at the beginning and end of the curvature. On the X-ray, the top and bottom vertebrae that form the spinal curve are selected. These vertebrae represent the beginning and ending points of the curvature. The top and bottom edges of each selected vertebra are drawn with lines, and an angle is measured through the intersection of these lines. This angle is considered the Cobb angle. Scoliosis can be diagnosed when the curvature in the spine is more than 10 degrees. If the Cobb angle is 10 degrees or more, this curvature is considered scoliosis.
Change from baseline severity of scoliosis at 12 weeks.
Change of Trunk Rotation Angle
Lasso di tempo: Change from baseline trunk rotation angle at 12 weeks.
Trunk rotation angle (ATR) will be measured using a Bunnell scoliometer. Frequently used to assess scoliosis progression and treatment effectiveness, the Bunnell scoliometer is an inclinometer known for its ease of use, low cost, and reliability. Measurements are taken by placing the scoliometer vertically along the axial axis of the vertebral column, perpendicular to the spinous processes of the vertebrae. In our study, assessments with the scoliometer will be performed in a standing forward-bend position. Patients will be asked to bend forward until the trunk is in a horizontal position and the scapula and pelvis are aligned. Care will be taken to ensure that the patients' arms are relaxed in this position. The highest rotation angle value obtained from the thoracic, thoracolumbar, and lumbar regions of the spine will be noted.
Change from baseline trunk rotation angle at 12 weeks.
Change of Cosmetic Deformity Perception
Lasso di tempo: Changes from baseline Cosmetic Deformity Perception at 12 weeks.
Patients' perception of cosmetic deformity will be assessed using the WRVAS (Walter Reed Visual Assessment Scale). WRVAS is a visual scale designed for patients with idiopathic scoliosis to describe how they perceive their own deformity. The scale categorizes deformity into 7 different aspects. Each of the 7 items includes a set of 5 figures representing the severity of the deformity. These sets contain visuals that assess spinal deformity, rib protrusion, lumbar protrusion, chest deformity, trunk imbalance, shoulder asymmetry, and scapular asymmetry. The visuals include posterior views of the deformity and assess how the patient feels about how others see their own back. Selected visuals are scored from a minimum of "1" to a maximum of "5". The results are used to understand the visual changes caused by scoliosis, as well as to monitor treatment outcomes. Reliability and validity studies were conducted on the Turkish version of the scale
Changes from baseline Cosmetic Deformity Perception at 12 weeks.
Change of Quality of Life
Lasso di tempo: Change from Baseline Quality of Life at 12 weeks.
The Scoliosis Research Society-22 (SRS-22) questionnaire is a widely used self-report scale developed to assess quality of life in individuals with adolescent idiopathic scoliosis and adult spinal deformities for clinical and research purposes. Originally derived from the SRS-24 version, this form has been simplified to shorten assessment time and reduce patient burden. Today, it is used as a standardized tool to understand how scoliosis affects an individual's daily life. Each item is evaluated using a Likert-type response scale scored from 1 (worst case) to 5 (best case). Higher scores indicate better quality of life. For example, a question such as "To what extent does your back pain affect your daily activities?" quantitatively reflects the impact of the pain experienced by the individual on daily functioning. In the overall scoring of the questionnaire, excluding the treatment satisfaction dimension, average sub-dimension scores are obtained out of 20 items.
Change from Baseline Quality of Life at 12 weeks.
Change of Electromyographic Activity of Muscles
Lasso di tempo: Change from Baseline Electromyographic Activities of Muscles at 12 weeks.
Muscles produce myoelectric potentials during contraction. Electromyography (EMG) is an evaluation method to determine the magnitude of this electrical activity of the muscle. Surface EMG signals are obtained with surface electrodes placed on the muscle body. High-magnitude EMG signals indicate that numerous motor units are firing. The magnitude of EMG signals provides information about how well the person can use the muscles being evaluated and the strength of the relevant muscle. Individuals with adolescent idiopathic scoliosis have asymmetric use and loss of strength in muscles. The main goal of the exercises used in treatment is to increase muscle strength, reduce asymmetric use, and increase the usability of the muscles. Evaluations will be performed with the wireless BTS FreeEMG-1000 system (BTS Engineering Corp.) electromyography device. The system has a miniaturized wireless surface EMG probe with Snap-On active electrodes that receive and transmit the signal in real time, and
Change from Baseline Electromyographic Activities of Muscles at 12 weeks.
Change of Pulmonary Function
Lasso di tempo: Change from Baseline Pulmonary Function at 8 weeks.
Description: The Pulmonary Function Test will be performed with the COSMED Pony FX (COSMED; Italy) spirometer in accordance with the criteria of the American Thoracic Society (ATS) and the European Respiratory Society (ERS). Forced vital capacity (FVC), Forced expiratory volume in 1 second (FEV1), Tiffeneau ratio (FEV1/FVC), Forced expiratory flow 25-75% (FEF25-75%) and peak expiratory flow rate (PEF) values and predictive values percentage will be recorded. Preoperative period, postoperative 7th day, postoperative 4th week and postoperative 8th week will be repeated.
Change from Baseline Pulmonary Function at 8 weeks.
Change of Respiratory Muscle Strength
Lasso di tempo: Change from Baseline Respiratory Muscle Strength at 12 weeks.
Respiratory muscle strength measurement will be performed with a portable, electronic intraoral pressure measuring device COSMED Pony FX (COSMED; Italy) according to ATS/ERS criteria. The MIP will be measured at residual volume and during deep inspiration. MEP will be determined at total lung capacity and during deep expiration. Measurements will be made in a sitting position using a nose clip. Patients will be verbally encouraged for the best strength. Measurement will be made until it provides the valid value in patients. Preoperative period, postoperative 7th day, postoperative 4th week and postoperative 8th week will be repeated.
Change from Baseline Respiratory Muscle Strength at 12 weeks.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Height in Meters
Lasso di tempo: Initial assessment before surgery
The height of all subjects in meters (m) will be noted before the surgery. Height will be combined to report BMI in kg/m^2
Initial assessment before surgery
Weight in Kilograms
Lasso di tempo: Initial assessment before surgery
The weight of all subjects in kilograms (kg) will be noted before the surgery. Weight will be combined to report BMI in kg/m^2.
Initial assessment before surgery
Body Mass Index (BMI) in kg/m^2
Lasso di tempo: Initial assessment before surgery
Description: Body Mass Index (BMI) will be calculated with the formula weight (kg)/height (m)^2.
Initial assessment before surgery

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Akdeniz University

Investigatori

  • Investigatore principale: Neriman Temel Aksu, Akdeniz University

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 agosto 2026

Completamento primario (Stimato)

1 febbraio 2027

Completamento dello studio (Stimato)

30 aprile 2027

Date di iscrizione allo studio

Primo inviato

23 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

1 luglio 2026

Primo Inserito (Effettivo)

6 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

1 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • akdenizscoliosis

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Descrizione del piano IPD

Patients and their relatives may not want this.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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