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Clinical efficacy study of Cheneau orthosis combined with Baduanjin in the intervention of adolescent idiopathic scoliosis

Clinical efficacy study of Cheneau orthosis combined with Baduanjin in the intervention of adolescent idiopathic scoliosis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095904
Enrollment
Unknown
Registered
2025-01-15
Start date
2025-02-13
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Adolescent idiopathic scoliosis

Interventions

experimental group:Brace treatment + Baduanjin intervention
Control group:Brace treatment

Sponsors

Shanghai Rehabilitation Center for Special Children
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 16 Years

Inclusion criteria

Inclusion criteria: (1) Patients aged 10-16 who meet the diagnostic criteria for adolescent idiopathic scoliosis; (2) Risser's sign 0-IV degree; (3) Cobb's angle: 25°- 40°; (4) have not received prior brace or surgical treatment; (5) voluntarily join the pilot study; (6) Able to cooperate with the data acquisition of the 3D motion capture system.

Exclusion criteria

Exclusion criteria: (1) Presence of serious underlying diseases; (2) Severe impairment of cognitive, verbal and auditory comprehension functions; (3) Rib or thoracic deformity cannot be matched with the brace.

Design outcomes

Primary

MeasureTime frame
Cobb angle;Thoracic Volume;

Secondary

MeasureTime frame
Gait kinematics parameters;Gait dynamics parameters;

Countries

China

Contacts

Public ContactMin Shen; Liang Qian

Shanghai Rehabilitation Center for Special Children; Shanghai University of Traditional Chinese Medicine

minshen223@qq.com+86 180 1888 0579

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026