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Application mechanism of neuroregulation combined with myoelectric biofeedback in the treatment of postural control disorders in adolescent patients with idiopathic scoliosis

Application mechanism of neuroregulation combined with myoelectric biofeedback in the treatment of postural control disorders in adolescent patients with idiopathic scoliosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075910
Enrollment
Unknown
Registered
2023-09-19
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-09-26

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

Conditions

scoliosis

Interventions

Neuroregulation joint brace training group:A hard brace is assessed and made by a prosthetist and worn for at least 16-18 hours per day as directed by the doctor and recorded. On this basis, one grou
Electromyobiofeedback combined brace training group:The patients' paravertebral muscle surface electromyography was observed under the monitoring of surface electromyography, and the patients were gui
PSEE Training Joint Brace Training Group:PSSE training was arranged according to the type of the patient s lateral curvature and the size of the Cobb Angle of the lateral curvature. The training conte
Healthy control group:NA

Sponsors

Kunming Medical University Rehabilitation School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1) Patients diagnosed with idiopathic scoliosis; 2) Aged from 10 years to 18 years (including 10 years); 3) Risser sign < Level 3 and below) 4) Cobb Angle 25-45° (main side bend); 5) Patients who have not previously received orthotics or surgery; 6) Signed informed consent before the experiment, informing patients that they can voluntarily opt out of the study if they have any discomfort during the treatment.

Exclusion criteria

Exclusion criteria: 1) Patients diagnosed with non-idiopathic scoliosis (congenital scoliosis, postural scoliosis, neuromuscular scoliosis, compensatory scoliosis, etc.); 2) Patients with complete growth and development (patients with height increase < 1cm within 6 months, patients with Risser sign =4, female patients with more than 2 years from menarche); 3) Patients with diseases that prevent them from exercising; 4) Patients with other cardiopulmonary diseases or dysfunction; 5) Patients with significant cognitive deficits who were unable to complete the SRS-22 and SF-36 questionnaires.

Design outcomes

Primary

MeasureTime frame
Cobb angle;Near infrared evaluation;Surface electromyography;Assessment of balance function;

Countries

China

Contacts

Public ContactMeng Fanyuan

Kunming Medical University Rehabilitation School

mengfanyuan@kmmu.edu.cn+86 150 9663 4903

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026