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Effect of Spiral Torsion Training on Vertebral Rotation and Three-Dimensional Deformity Correction in Adolescent Idiopathic Scoliosis: A Randomized Controlled Trial

Effect of Spiral Torsion Training on Vertebral Rotation and Three-Dimensional Deformity Correction in Adolescent Idiopathic Scoliosis: A Randomized Controlled Trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124767
Enrollment
Unknown
Registered
2026-05-18
Start date
2026-05-22
Completion date
Unknown
Last updated
2026-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

adolescentidiopathicscoliosis

Interventions

Experimental group:Spiral Rotation Training

Sponsors

Geriatrics Hospital of hainan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Age 10–18 years, any sex. 2. Diagnosed as AIS by standing full-spine AP and lateral X-rays. 3. Main curve Cobb angle 10°–40°. 4. Lenke classification types 1–6. 5. Risser sign grade 0–4, still possessing some potential for growth. 6. No prior spinal surgery and no systemic PSSE training within the past 3 months. 7. The subject is capable of understanding and complying with the training and assessments; minors must have informed consent signed by their legal guardian, and the subject must sign an informed consent acknowledgement/statement of agreement to participate.

Exclusion criteria

Exclusion criteria: 1. Congenital, neuromuscular, syndromic, or other non-idiopathic scoliosis. 2. Prior history of spinal surgery, or planning to undergo spinal surgery during the study period. 3. Concurrent severe cardiac, pulmonary, neurological, or musculoskeletal diseases that would make it unsafe to complete exercise training or cardiopulmonary exercise testing. 4. Presence of significant cognitive impairment, psychiatric or behavioral disorders, or severely poor compliance, rendering the participant unable to understand or cooperate with study requirements. 5. Participation in other clinical studies or systematic exercise intervention programs within the past 3 months. 6. Any other circumstances that the investigator judges make the participant unsuitable for this study.

Design outcomes

Primary

MeasureTime frame
Cobb angle;Axial rotation angle of the atlas;

Secondary

MeasureTime frame
Angle of trunk rotation;Maximum oxygen uptake;SRS-22 Questionnaire;Peak oxygen consumption adjusted for body weight;Anaerobic Threshold ;

Countries

China

Contacts

Public ContactChen Zeng

Wuhan Sports University Hainan Provincial Geriatric Hospital

2024420038@whsu.edu.cn+86 898 3192 1458

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026