Idiopathic Scoliosis (mild to moderate). Adolescent idiopathic scoliosis, thoracolumbar region
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adolescent girls aged 15 to 18 years C-shaped thoracic adolescent idiopathic scoliosis Cobb angle between 10 and 25 degrees (mild to moderate severity) right hand as the dominant hand
Exclusion criteria
Exclusion criteria: Any history of spinal surgery history of a condition that has led to scoliosis or other spinal deformities use of a brace presence of neurological or orthopedic disease or disorder having fixed structural scoliosis with visible deformity during the Adam’s forward bend test shortening of any lower limb
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Lumbopelvic motor performance. Timepoint: Measurements will be conducted at the beginning of the study, after the 12-week intervention protocol, and following a 12-week follow-up period. Method of measurement: To assess the motor performance of the lumbopelvic-hip complex, the Abduction Drop (Ober) test, Extension Drop (Thomas) test, trunk rotation range of motion, and hip joint range of motion tests are used.;Lumbopelvic hip kinematic parameters. Timepoint: Measurements will be conducted at the beginning of the study, after the 12-week intervention protocol, and following a 12-week follow-up period. Method of measurement: To evaluate certain kinematic parameters of the lumbopelvic-hip complex, the Standing Reach test, Full Squat test, and a motion analysis system based on IMU sensors are utilized.;Spinal deviation angle. Timepoint: Measurements will be conducted at the beginning of the study, after the 12-week intervention protocol, and following a 12-week follow-up period. Method of measurement: Spinal deviation angle will be assessed by Cobb angle using spinal photogrammetry from the posterior view and trunk rotation measured using a scoliometer during the Adams test. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life. Timepoint: Measurements will be conducted at the beginning of the study, after the 12-week intervention protocol, and following a 12-week follow-up period. Method of measurement: SRS-22 questionnaire.;Spinal and pelvic girdle pain. Timepoint: Measurements will be conducted at the beginning of the study, after the 12-week intervention protocol, and following a 12-week follow-up period. Method of measurement: SRS-22 questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
University of Guilan