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Clinical efficacy study of a multifunctional spinal stretching therapy system

Clinical efficacy study of a multifunctional spinal stretching therapy system

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000228
Enrollment
Unknown
Registered
2024-08-13
Start date
2023-06-01
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Idiopathic Scoliosis

Interventions

Experimental group: Basic exercise therapy Multifunctional spinal distraction treatment system treatment
Experimental group:Basic exercise therapy Multifunctional spinal distraction treatment system treatment

Sponsors

Rehabilitation Hospital affiliated to Fujian University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 22 Years

Inclusion criteria

Inclusion criteria: (1) meet the diagnostic criteria for idiopathic scoliosis, (2) age 10-22 years old (including 10 years old, including 22 years old), regardless of gender, (3) X-ray screening Cobb angle within 10-25° (excluding 10°, excluding 25°), (4) scoliosis progression factor = 1.6. Formula: [Cobb angle - (Risser's sign × 3)]/age; (5) Sign the informed consent form and voluntarily participate in this trial;

Exclusion criteria

Exclusion criteria: (1) Congenital, neuromuscular, neurofibroma, interstitial lesions and traumatic scoliosis; (2) Accompanied by severe osteoporosis and other diseases that are not suitable for stretching treatment; (3) Patients with suspected or diagnosed spinal joint, soft tissue and neuraxial tumors; (4) Patients with suspected or confirmed spinal instability such as spondylolisthesis; (5) Patients with severe skin injury, bleeding or skin disease in the spine area; (6) Those with a true leg length difference of more than 2cm in both lower limbs (measurement method: take a tape measure, one end is fixed in the greater trochanter, and the other end is read at the tip of the medial malleolus, and the leg length difference is more than 2cm is excluded.) ); (7) Those who are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Cobb angle;

Secondary

MeasureTime frame
Angle of Trunk rotation(ATR);ScoliosIS Research Society-22 (SRS-22);spinal appearance questionnaire(SAQ);

Countries

China

Contacts

Public ContactXiaowen Lian

Rehabilitation Hospital affiliated to Fujian University of Traditional Chinese Medicine

277033616@qq.com+86 182 5017 8186

Outcome results

None listed

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