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To investigate the effect of Flexi-bar training on delayed activation of core muscle group in patients with chronic non-specific low back pain and its neuromuscular mechanism

To investigate the effect of Flexi-bar training on delayed activation of core muscle group in patients with chronic non-specific low back pain and its neuromuscular mechanism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096032
Enrollment
Unknown
Registered
2025-01-16
Start date
2025-02-01
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

Chronic non-specific low back pain

Interventions

Low back pain group:Flexi-bar training
Healthy group:None

Sponsors

The Affiliated Panyu Central Hospital, Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1.In line with the "Chinese Expert consensus on the diagnosis and treatment of acute/chronic non-specific low back pain"; 2.Patients with stable vital signs, unconscious cognitive impairment, and informed consent; 3.Age 18~45 years old, disease duration >=3 months, and no exercise therapy in the past 1 month; 4.There was no abnormality in imaging examination, radiation pain in lower limbs and nerve root compression symptoms. 5.Body mass index (BMI) between 18.5~25kg/m²; 6.The numerical pain scale (VAS) was 3~7; 7.Right handed.

Exclusion criteria

Exclusion criteria: 1.Patients with spinal dislocation, fracture, severe trauma and surgical history; 2.Patients with lumbar fusion and severe osteoporosis; 3.Lumbar soft tissue tumors and tuberculosis; 4.Patients with severe primary diseases of heart, lung, liver and kidney and cognitive impairment; 5.Women in pregnancy, lactation, menstrual period or with long-term dysmenorrhea; 6.Diseases affecting the musculoskeletal system, such as bony spinal stenosis, ankylosing spondylitis, intervertebral disc herniation, severe arthritis, etc. ?VAS more than 8 points; 7.VAS more than 8 points;

Design outcomes

Primary

MeasureTime frame
Relative activation time;Blood flow in the motor cortex;Muscle thickness;

Secondary

MeasureTime frame
Visual Analog Scale for Pain;Mean motion speed for sway in the forward and left and right directions;Oswestry Disability Index;

Countries

China

Contacts

Public Contactluowei

The Affiliated Panyu Central Hospital, Guangzhou Medical University

289369282@qq.com+86 20 34859327

Outcome results

None listed

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