- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06417944
The Effect of Three-dimensional Exercise (Schroth Exercise) on Diaphragm Thickness in Adolescent Idiopathic Scoliosis Patients
Study Overview
Status
Detailed Description
Spinal deformity is common in childhood and adolescence, and can often present as scoliosis or increased thoracic kyphosis deformity with various etiologies.
Any spinal deformity, especially one that affects the thoracic spine, can affect lung function. If left untreated, the curves may distort over time as skeletal growth accelerates. In some patients, this can lead to restrictive or obstructive lung disease and, rarely, death as a result of cor pulmonale.
The alignment of the skeletal system in the chest and its harmony with the compliance of the chest wall are related to respiratory function; Thoracic kyphosis and the resulting changes in the rib cage lead to a decrease in lung capacity. The diaphragm is the main respiratory muscle, and diaphragm contraction is associated with respiratory functions. In recent years, ultrasonography (USG) has gained increasing utility for visualizing the diaphragm and assessing its function, with several advantages.
In the planned thesis study, investigators will measure the diaphragm thickness in adolescent idiopathic scoliosis patients with scoliosis deformities affecting the thoracic region, whether there is any relationship between the impact in the thoracic region and the diaphragm thickness, and the three-dimensional exercise (Schroth exercise-Barcelona Schroth therapy) applied in investigators' clinic for scoliosis, before and after the treatment of the diaphragm. Investigators aimed to show whether there is any change in thickness.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Gaziosmanpasa
-
Istanbul, Gaziosmanpasa, Turkey, 34255
- Omer Faruk Alp
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Having scoliosis affecting the thoracic region according to BSPTS (type 3C, type 4C and its subtypes)
- Being between the ages of 10-18
- Being able to perform a respiratory function test
- Having the mental capacity to answer surveys
Exclusion Criteria:
- Congenital spinal, costal and diaphragmatic anomalies
- Neuromuscular disease
- Respiratory system diseases that affect lung functions
- Patients who cannot cooperate with spirometry.
- Having surgery to the chest wall or spine
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Schroth group (Group 1)
Patients aged 10-18 years who are diagnosed with scoliosis and given 10 sessions of schroth exercises, either outpatient or inpatient. Scoliosis study forms consisting of clinical and radiological measurements of patients aged 10-18 years who applied to the outpatient clinic with spine deformity will be filled in in detail. |
Scoliosis study form consisting of clinical and radiological measurements of patients aged 10-18 years who applied to the outpatient clinic with spine deformity will be filled in detail.
Patients whose Adam's forward bending test and clinical evaluation results are compatible with scoliosis, scoliosis graphy are requested.
(Adams test (forward bending test) (+) was measured by Bunnell scoliometer (scoliosis assessment tool) and ATR (angle of trunk rotation angle) values were 5 degrees in those with BMI (Body Mass Index) above 85%.
If it is below 85% and above 7 degrees, patients who meet the inclusion criteria will be included in the study by filling out an informed consent form and a scoliosis film will be requested.).Coronal, sagittal balance; coronal and sagittal Cobb angles will be measured from posterior-anterior (PA) and lateral scoliosis radiographs.
Pulmonary function tests (PFTs) are noninvasive tests that show how well the lungs are working.
The tests measure lung volume, capacity, rates of flow, and gas exchange.
This information can help your healthcare provider diagnose and decide the treatment of certain lung disorders.
We will use handheld spirometry device for measurement.
Three measurements will be made.
In these three measurements; FEV1(Forced Expiratory Volume In One Second)(L), FEV1 (%predicted), FVC (Forced Vital Capacity) (L), FVC (%predicted), FEV1/FVC (%) and FEV1/FVC (%predicted) will be evaluated.
The arithmetic average of the results of these three measurements will be taken.
Other Names:
Diaphragm thickness will be measured in the supine position with a 6-14 Mhz lineer, conventional ultrasound probe (Mindray DC-8, Shenzen Mindray Bio-Medical Electronics CO. LTD.,P.R. China) at the end of inspiration and expiration from the intercostal space on the anterior axillary line.
The measurements will be evaluated by making three measurements from the right 8-9. intercostal space where the diaphragm is best visualized.
End-expiratory (Forced residual capacity-FRC) (centimeter- cm), end-inspiratory (Total Lung Capacity) (centimeter-cm) and thickening rate (%) (thickness TLC / thickness FRC) will be evaluated three times and the arithmetic average of these three measurements will be taken.
It only provides outpatient treatment, but it has different practices, intensive or regular, depending on local and external patients. For local patients, it is applied once a week, accompanied by a therapist, and the treatment duration is determined according to the patient's condition. In patients coming from outside; It can be continued as 2 hours a day for 10 days, then as additional treatment for 1-2 weeks for 3-6 months depending on the patient's condition. I In regular treatment; 30 sessions of 90 minutes group treatment, the first 8 sessions are carried out under the supervision of a therapist for a shorter period of time. We will give 10 sessions of BSPTS Schroth exercises, either outpatient or inpatient. After 10 sessions of the Schroth exercise program, the home program will continue two months after outpatient/inpatient schroth exercise(Home program: 5 days/week, 45-60 minutes for all patients).
Other Names:
|
|
Control group (Group 2)
Patients aged 10-18 years who are diagnosed with scoliosis and given home exercise Scoliosis study forms consisting of clinical and radiological measurements of patients aged 10-18 years who applied to the outpatient clinic with spine deformity will be filled in in detail.
|
Scoliosis study form consisting of clinical and radiological measurements of patients aged 10-18 years who applied to the outpatient clinic with spine deformity will be filled in detail.
Patients whose Adam's forward bending test and clinical evaluation results are compatible with scoliosis, scoliosis graphy are requested.
(Adams test (forward bending test) (+) was measured by Bunnell scoliometer (scoliosis assessment tool) and ATR (angle of trunk rotation angle) values were 5 degrees in those with BMI (Body Mass Index) above 85%.
If it is below 85% and above 7 degrees, patients who meet the inclusion criteria will be included in the study by filling out an informed consent form and a scoliosis film will be requested.).Coronal, sagittal balance; coronal and sagittal Cobb angles will be measured from posterior-anterior (PA) and lateral scoliosis radiographs.
Pulmonary function tests (PFTs) are noninvasive tests that show how well the lungs are working.
The tests measure lung volume, capacity, rates of flow, and gas exchange.
This information can help your healthcare provider diagnose and decide the treatment of certain lung disorders.
We will use handheld spirometry device for measurement.
Three measurements will be made.
In these three measurements; FEV1(Forced Expiratory Volume In One Second)(L), FEV1 (%predicted), FVC (Forced Vital Capacity) (L), FVC (%predicted), FEV1/FVC (%) and FEV1/FVC (%predicted) will be evaluated.
The arithmetic average of the results of these three measurements will be taken.
Other Names:
Diaphragm thickness will be measured in the supine position with a 6-14 Mhz lineer, conventional ultrasound probe (Mindray DC-8, Shenzen Mindray Bio-Medical Electronics CO. LTD.,P.R. China) at the end of inspiration and expiration from the intercostal space on the anterior axillary line.
The measurements will be evaluated by making three measurements from the right 8-9. intercostal space where the diaphragm is best visualized.
End-expiratory (Forced residual capacity-FRC) (centimeter- cm), end-inspiratory (Total Lung Capacity) (centimeter-cm) and thickening rate (%) (thickness TLC / thickness FRC) will be evaluated three times and the arithmetic average of these three measurements will be taken.
In the home exercise program; daily living activities, neutral pelvis exercises, coronal balance exercises, rotational angular breathing exercises and axial elongation exercises were taught by the physiotherapist in one session.
A total of 10-week home exercise program was planned, with exercises to be performed twice a week for the first two weeks, once every 15 days for 1 month (twice in one month), and then once a month.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Scoliosis study form
Time Frame: Within 2 week of applying to the scoliosis outpatient clinic
|
Scoliosis study form consisting of clinical and radiological measurements of patients aged 10-18 years who applied to the outpatient clinic with spine deformity will be filled in detail.
|
Within 2 week of applying to the scoliosis outpatient clinic
|
|
Pulmonary function test
Time Frame: Within 2 weeks after applying to the scoliosis clinic (pre-exercise) and 3 months after exercise
|
We will use handheld spirometry device for measurement.
Three measurements will be made.
In these three measurements; FEV1(Forced Expiratory Volume In One Second) (Liter-L), FEV1 (%predicted), FVC (Forced Vital Capacity) (Liter-L), FVC (%predicted), FEV1/FVC (%) and FEV1/FVC (%predicted) will be evaluated.
The arithmetic average of the results of these three measurements will be taken.
|
Within 2 weeks after applying to the scoliosis clinic (pre-exercise) and 3 months after exercise
|
|
Ultrasonographic Diaphragm Thickness Measurement
Time Frame: Within 2 weeks after applying to the scoliosis clinic(pre-exercise) and 3 months after exercise
|
Diaphragm thickness (millimeter-mm) will be measured in the supine position with a 6-14 Mhz lineer, conventional ultrasound probe (Mindray DC-8, Shenzen Mindray Bio-Medical Electronics CO. LTD.,P.R. China) at the end of inspiration and expiration from the intercostal space on the anterior axillary line.
The measurements will be evaluated by making three measurements from the right 8-9. intercostal space where the diaphragm is best visualized.
Diaphragm thickness of End-expiratory (Forced residual capacity-FRC) (millimeter-mm), diaphragm thickness of end-inspiratory (Total Lung Capacity) (millimeter-mm) and thickening rate (%) (thickness TLC / thickness FRC) will be evaluated three times and the arithmetic average of these three measurements will be taken.
|
Within 2 weeks after applying to the scoliosis clinic(pre-exercise) and 3 months after exercise
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Pediatric Quality of Life Inventory
Time Frame: Within 2 weeks after applying to the scoliosis clinic(pre-exercise) and 3 months after exercise
|
The Pediatric Quality of Life Inventory (PedsQL) is a 23-item generic health status instrument with parent and child forms that assesses five domains of health (physical functioning, emotional functioning, psychosocial functioning, social functioning, and school functioning) in children and adolescents ages 2 to 18.
Each item of the instrument is scored on a 5-point scale from 0- 4 for ages 8-18, (0 = never a problem, 1 = almost never a problem, 2 = sometimes a problem, 3 = often a problem, 4 = almost always a problem) ad 3-point scale for young child self reporting (ages 5- 7) as following (0 = not at all a problem, 2 = sometimes a problem, 4 = a lot of a problem) the large score means worst symptoms , scores are linearly transformed to a 0-100 scale (0 = 100, 1 = 75, 2 = 50, 3 = 25, 4 = 0) in which high score means better condition
|
Within 2 weeks after applying to the scoliosis clinic(pre-exercise) and 3 months after exercise
|
|
Scoliosis Research Society Score
Time Frame: Within 2 weeks after applying to the scoliosis clinic(pre-exercise) and 3 months after exercise
|
The SRS-22r is a validated questionnaire intended to assess outcomes in patients with idiopathic scoliosis after spinal surgery.
The first version, developed by the Scoliosis Research Society in 1999, had 24 items, and this was reduced to 22 items (accompanied by a name change) in the course of 3 major updates.The SRS-22 contains 22 questions covering 5 domains: function/activity 5 items; pain 5 items; self-perceived image 5 items; mental health 5 items; and satisfaction with treatment 2 items.
Each item is scored from 1 (worst) to 5 (best).
Each domain has a total sum score ranging from 5 to 25, except for satisfaction, which ranges from 2 to 10.
The sum of the first 4 domains gives a maximum subtotal of 100, and when the satisfaction domain is included, the maximum total is 110
|
Within 2 weeks after applying to the scoliosis clinic(pre-exercise) and 3 months after exercise
|
Collaborators and Investigators
Investigators
- Study Chair: Aynur Metin Terzibasioglu, MD,Chief Assistant, Maltepe District, Askeri Firin Street, Inistanbul buildins F1 Block Flat: 82 Zeytinburnu /ISTANBUL
- Study Director: Ebru Yilmaz Yalcinkaya, MD,Professor, Gaziosmanpasa Training and Research Hospital Physical Rehabilitation Department
Publications and helpful links
General Publications
- Jagger F, Tsirikos AI, Blacklock S, Urquhart DS. Adaptation to reduced lung function in children and young people with spinal deformity. J Clin Orthop Trauma. 2020 Mar-Apr;11(2):191-195. doi: 10.1016/j.jcot.2019.12.013. Epub 2020 Jan 3.
- Karaali E, Ciloglu O, Gorgulu FF, Ekiz T. Ultrasonographic measurement of diaphragm thickness in patients with severe thoracic scoliosis. J Ultrasound. 2021 Mar;24(1):75-79. doi: 10.1007/s40477-020-00536-w. Epub 2021 Feb 7.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 326
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Scoliosis
-
National Scoliosis CenterCompletedAdolescent Idiopathic Scoliosis (AIS) | Neuromuscular Scoliosis | Juvenile Idiopathic Scoliosis | Infantile Idiopathic Scoliosis | Ealy Onset ScoliosisUnited States
-
Manhattan Physical Medicine and Rehabilitation,...RecruitingScoliosis Idiopathic | Scoliosis; Adolescence | Scoliosis; Lumbar RegionUnited States
-
Istanbul University - Cerrahpasa (IUC)RecruitingScoliosis | Adolescent Idiopathic Scoliosis | Scoliosis; Adolescence | Scoliosis Lumbar RegionTurkey
-
Lahore University of Biological and Applied SciencesGhurki Trust and Teaching HospitalNot yet recruitingScoliosis Idiopathic | Idiopathic Adolescent ScoliosisPakistan
-
Poznan University of Medical SciencesNot yet recruitingScoliosis Idiopathic | Scoliosis; AdolescencePoland
-
Uppsala UniversityUniversity of Oslo; Linkoeping University; Örebro University, Sweden; Skane University... and other collaboratorsNot yet recruitingIdiopathic Adolescent Scoliosis | Idiopathic Juvenile ScoliosisSweden
-
EUROSRecruitingScoliosis Idiopathic | Consent Forms | Scoliosis NeuromuscularFrance
-
Deep Health Ltd.Not yet recruitingScoliosis | Scoliosis; Adolescence | Scoliosis Lumbar Region | Pathologic Fracture | Scoliosis Kyphosis | Scoliosis Thoracic RegionUnited Kingdom
-
Boston Children's HospitalChildren's Hospital Colorado; University of Florida; Cedars-Sinai Medical Center and other collaboratorsRecruitingAdolescent Idiopathic Scoliosis | Idiopathic Scoliosis | Spondylolisthesis | Spine Deformity | Neuromuscular Scoliosis | Congenital ScoliosisUnited States
-
Assistance Publique - Hôpitaux de ParisRecruitingScoliosis | Scoliosis Idiopathic | Scoliosis NeuromuscularFrance
Clinical Trials on Scoliosis study form
-
Gaziosmanpasa Research and Education HospitalNot yet recruitingSpine Deformity | Adult Scoliosis | PeloidotherapyTurkey (Türkiye)
-
Gaziosmanpasa Research and Education HospitalCompletedSpine Deformity | Diaphragm Issues | HyperkyphosisTurkey
-
Gaziosmanpasa Research and Education HospitalRecruitingAdolescent | Sleep Quality | Kyphosis | Spine Deformity | Trunk Muscle EnduranceTurkey (Türkiye)
-
Gaziosmanpasa Research and Education HospitalCompletedSpinal Deformity | Pectus Deformity of ChestTurkey
-
Radicle ScienceCompleted
-
Radicle ScienceCompletedCognitive FunctionUnited States
-
Radicle ScienceCompletedFatigue | EnergyUnited States
-
Radicle ScienceCompletedCognitive FunctionUnited States
-
Radicle ScienceCompletedStress | AnxietyUnited States
-
Radicle ScienceCompletedSleep Disorder | Sleep | Sleep DisturbanceUnited States