Single center, double blinded, prospective crossover randomized controlled trial. To clinically validate the efficacy of nighttime braces designed automatically by a generative design algorithm to treat idiopathic scoliosis (IS). The tested hypothesis was the clinical equivalence of immediate in-brace correction for the new automatically generated brace design versus a standard Providence-type brace. Documented efficacy of brace treatment varies between centers, and depends on the empirical expertise of the treating orthotist. Our group previously developed a fully-automated generative brace design algorithm that leverages a patient-specific finite element model (FEM) to optimize brace geometry and correction before its fabrication. Fifty-eight skeletally immature patients diagnosed with IS, aged between 10 to 16 years were recruited. All patients received both a nighttime brace automatically generated by the algorithm (Test) and a Providence-type brace designed by an expert orthotist (Control). Radiographs were taken for each patient with both braces in a randomized crossover approach to evaluate immediate in-brace correction. The targeted fifty-five patients (48 females, 7 males) completed the study. The immediate Cobb angle correction was 57% ± 19 (Test) versus 58% ± 21 (Control) for the main thoracic (MT) curve, while it was 89% ± 25 (Test) versus 87% ± 28 (Control) for the thoraco-lumbar/lumbar (TLL) spine. The immediate correction with the Test brace was non-inferior to that of the Control brace (P < 0.001). The order in which the braces were tested did not have a residual effect on the immediate correction. The fully-automated generative brace design algorithm proves to be clinically relevant, allowing for immediate in-brace correction equivalent to that of braces designed by expert orthotists. Patient 2 years follow-up will continue. This method's integration could help design and rationalize the design of braces for the treatment of IS. Level 2.