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Efficacy of sensorimotor training combined with core strength training for low back pain in adult idiopathic scoliosis: a randomized controlled trial

Efficacy of sensorimotor training combined with core strength training for low back pain in adult idiopathic scoliosis: a randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085370
Enrollment
Unknown
Registered
2024-06-06
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

adult idiopathic scoliosis

Interventions

CST therapy group:core strength training
SMT therapy group:sensorimotor training
Combination therapy group:core strength training combined with sensorimotor training

Sponsors

Xinhua Hospital Afiliated to Shanghai Jiaotong University School Of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1.Age is between 18 and 40 years; 2.The Cobb angle is 10° or greater, and the etiology is unknown; 3.Patients complain of lower back pain (located between the twelfth rib on the dorsal side of the body and the subgluteal crease) that is severe enough to limit daily activities or alter the daily routine for more than one day; 4.Lower back pain has occurred within the past four weeks; 5.Patients have the ability to communicate and follow instructions; 6.Patients understand the treatment plan and have given written informed consent.

Exclusion criteria

Exclusion criteria: 1.Scoliosis of defined etiology such as neuromuscular disorders, congenital disorders, and specific syndromes; 2.Patients with no prior exposure to any form of CST or SoMT; 3. Patients have a history of infection, tumor, and are pregnant or within 3 months of delivery; 4.Patients have a history of chest, abdominal, spinal, pelvic, and lower extremity surgery, or are scheduled to undergo surgery in the appropriate area during the treatment period; 5. Presence of clear contraindications to exercise or mental disorders; 6. Patients concurrently participate in other types of scoliosis or lower back pain treatment during the trial evaluation period.

Design outcomes

Primary

MeasureTime frame
Subjective pain scores;

Secondary

MeasureTime frame
Pain-related dysfunction;Indicators related to spine morphology;Postural Control;Proprioceptive sensitivity;quality of life;

Countries

China

Contacts

Public ContactXin Li

Xinhua Hospital Afiliated to Shanghai Jiaotong University School Of Medicine

lixin02@xinhuamed.com.cn+86 151 2100 7776

Outcome results

None listed

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