M41.10
Conditions
Interventions
Group 1: In the intervention group, the therapeutic success of the three-dimensional scoliosis treatment according to Katharina Schroth is determined after a four-week intensive rehabilitation. For th
Sponsors
Asklepios Katharina-Schroth Klinik
Eligibility
Sex/Gender
All
Age
10 Years to 18 Years
Inclusion criteria
Inclusion criteria: adolescent idiopathic scoliosis 10-18 years four-week rehabilitation or presentation at the outpatient clinic of the Asklepios Katharina-Schroth-clinic
Exclusion criteria
Exclusion criteria: neuromuscular scolioses congenital scolioses infantile and juvenile scoliosis secondary scolioses patients with mental retardation patients with spinal fusion surgery patients with reported pain at rest above a score of 5 on the visual analogue scale from 0 (no pain) to 10 (most severe pain imaginable) patients with an acute medical condition, such as fever, unhealed injuries, dizziness, nausea or balance problems patients taking medications that affect vigilance, muscle tone or the central nervous system patients who are (possibly) pregnant patients who do not have the capacity to give consent or to be informed, unless this condition is due to their age and there is informed consent from their legal representative or guardian. patients with a BMI >23 kg/m² (27) patients with a scoliosis > 50°(1, 27) high thoracic scolioses with a vertebra between TH2 and TH6
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Does a four-week intensive three-dimensional scoliosis treatment according to Katharina Schroth achieve a change in curvature angles compared to a control group? | — |
Secondary
| Measure | Time frame |
|---|---|
| Determination of a reliable and valid correlation factor for the determination of the Cobb angle. | — |
Countries
Germany
Contacts
Public ContactOmar Zabar
Asklepios Katharina-Schroth Klinik
Outcome results
None listed