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Idiopathic scoliosis is a living problem that resists correction. The underlying cause of the such disorder is unknown but directed more toward muscular disorders. However recent clinical observation showed a possible neuromuscular compromise early in those patients. The main purpose of this study is to develop a treatment procedure to correct the degree of bony curvature in patients with Idiopathic scoliosis through developing a neuromuscular corrective approach that might be a more effective conservative treatment protocol for such disorder.
Scoliosis is one of the most common spinal deformities occurring in school-going children during the growth spurts of adolescents. It is an abnormal curvature of the spine. Failure of early management of idiopathic scoliosis could lead to multiple problems related to postural malalignment, pulmonary and physical dysfunctions, and surgical interventions. These problems could lead to health-related quality-of-life issues such as psychological and social problems that are represented in social isolation, depression, loss of self-confidence, limited job opportunities, and hospital stays & days off school and university as a result of undergoing corrective surgeries. Treatment methods for adolescent idiopathic Scoliosis (AIS) vary between surgical intervention and conservative treatment, in mild and moderate cases. Conservative treatment includes physical therapy in addition to rigid splints and braces, which may cause pain, tightness, restriction of movement, and a bad psychological status for adolescents which may lead them to the irregular wearing of these splints and braces. A type of soft, lightweight, breathable orthosis which is TheraTogs orthotic undergarment with the strapping system has been fabricated to provide gentle, passive compression to correct spinal deformities. Therefore, the objective of this study is to evaluate the effectiveness of TheraTogs orthotic undergarment with the strapping system on controlling and modulating the degree of scoliosis in Saudi adolescents with idiopathic scoliosis.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control Group | Active Comparator | Adolescents in the control group will receive a scoliosis-specific exercise program which will be prescribed to control the progression of the scoliotic curve |
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| Experimental Group | Experimental | Adolescents in the experimental group will receive a scoliosis-specific exercise program which will be prescribed to control the progression of the scoliotic curve in addition to wearing the soft orthoses with external strapping. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Scoliosis-Specific Exercise Program | Other | Adolescents in the control group will receive a scoliosis-specific exercise program which will be prescribed to control the progression of the scoliotic curve. This exercise program will include frontal plane active or passive correction exercises for scoliotic posture. The exercise program for every participant will be three sessions per week for 12 successive weeks. Every treatment session was applied for one hour.The exercise program for every participant will be three sessions per week for 12 successive weeks. Every treatment session was applied for one hour. The exercise program for every participant will be three sessions per week for 12 successive weeks. Every treatment session was applied for one hour. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in the scoliotic cobb's angle (°) | X-ray imaging will be measured by a radiologist | [Data was collected at baseline, and 12 weeks after intervention commencement.] |
| Changes in the Pelvic Obliquity (mm) | The following device (DIERS Formetric 3D/4D spine & posture analysis system) will be used to examine the changes in the spinal vertebral parameters in different planes (sagittal, coronal and transverse). This device supplies a thorough report about the alignment of the whole spine in one assessment session. | [Data was collected at baseline, and 12 weeks after intervention commencement.] |
| Change in the vertebral rotation (Angle) | The following device (DIERS Formetric 3D/4D spine & posture analysis system) will be used to examine the changes in the spinal vertebral parameters in different planes (sagittal, coronal and transverse). This device supplies a thorough report about the alignment of the whole spine in one assessment session. | [Data was collected at baseline, and 12 weeks after intervention commencement.] |
| Change in the Coronal imbalance (mm) | The following device (DIERS Formetric 3D/4D spine & posture analysis system) will be used to examine the changes in the spinal vertebral parameters in different planes (sagittal, coronal and transverse). This device supplies a thorough report about the alignment of the whole spine in one assessment session. | [Data was collected at baseline, and 12 weeks after intervention commencement.] |
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The inclusion criteria will be:
The exclusion criteria will be:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Ehab M Abd El Kafy, PhD | Contact | +966531698541 | emkafy@uqu.edu.sa |
| Name | Affiliation | Role |
|---|---|---|
| Ehab M Abd El Kafy, PhD | Department of Physical Therapy- Faculty of Applied Medical Sciences - Umm Al Qura University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Umm Al Qura University | Recruiting | Mecca | Mecca Region | 21955 | Saudi Arabia |
- The data available is Case-by-case basis at the discretion of the Primary Sponsor
Start Date: Beginning one year following main results publication End Date: Ending two years following main results publication
Data can be obtained by Principal Investigator Email Address: emkafy@uqu.edu.sa
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| ID | Term |
|---|---|
| D012600 | Scoliosis |
| ID | Term |
|---|---|
| D013121 | Spinal Curvatures |
| D013122 | Spinal Diseases |
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
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| Soft orthoses with external strapping. | Other | Adolescents in the experimental group will receive a scoliosis-specific exercises program which will be prescribed to control the progression of the scoliotic curve in addition to wearing the soft orthoses with external strapping. The wearing schedule of the soft orthosis with the external strapping for every participant in this group will be 12 hours daily for 12 successive weeks. |
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