The objective of this study is to evaluate clinical effectiveness and the effect on quality of life of an inelastic thoracolumbarasacral orthosis in male and female hyperkyphotic patients with moderate to severe back pain disability and to demonstrate the safety of the intervention through detailed reporting and analysis of adverse events.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
16
Thoracolumbarsacral orthosis
Mean difference in the Oswestry Disability Index Scores of the intervention versus control groups
Time frame: 4 weeks
Measured amount of opioid medication consumed in the intervention group versus control group
Time frame: Baseline and weeks 2,3,4,8,12,16,20 and 24
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.