Introduction: The Scoliosis Research Society-30 (
SRS
-30) is a questionnaire originally developed from the
SRS
-22r questionnaire and is used to evaluate adolescent idiopathic scoliosis (AIS). It comprised questions on five domains: function, pain, self-image, mental health, and satisfaction, with seven additional questions related to postoperative aspects. In addition to the original English version, translations in multiple languages have been effectively applied. Herein, we evaluated the internal consistency and external validity of the Japanese version of the
SRS
-30 for AIS patients.
Methods: Among the 30 questions in
SRS
-30, the eight additional questions from
SRS
-22r were translated and back-translated to create a Japanese version of the
SRS
-30. This translated questionnaire was then used to survey patients with AIS who underwent corrective fusion surgery one year postoperatively. The internal consistency of the responses was evaluated using the Cronbach α coefficient. Additionally, the Spearman correlation analyses were conducted to assess the correlation between the scores obtained from the
SRS
-30 Japanese version and
SRS
-22r and the Oswestry Disability Index (ODI) for the overall scale and the five domains.
Results: A total of 81 cases (eight males and 73 females; mean age at surgery 14.4 years) were enrolled. The mean preoperative Cobb angle was 51.0°. The Cronbach α coefficient for the overall
SRS
-30 was 0.861, indicating high internal consistency, while the coefficients for each domain were as follows: function/activity, 0.697; pain, 0.405; self-image/appearance, 0.776; mental health, 0.845; and satisfaction, 0.559. The
SRS
-30 total score significantly correlated with the
SRS
-22r total (r=0.945, P<0.001) and the ODI (r=−0.511, P<0.001). The
SRS
-30 domains highly correlated with the corresponding
SRS
-22r domains, with correlations ranging from r=0.826 to 0.901 (all P<0.001).
Conclusions: The Japanese version of the
SRS
-30 demonstrated good internal and external validity. The
SRS
-30 can be used as an assessment tool for health-related quality of life in AIS patients.
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