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Neuromuscular Mechanisms of "Lumbar Three Needles" on Anticipatory Postural Adjustments in Chronic Low Back Pain: A Multimodal Synchronization Study

Neuromuscular Mechanisms of "Lumbar Three Needles" on Anticipatory Postural Adjustments in Chronic Low Back Pain: A Multimodal Synchronization Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000520
Enrollment
Unknown
Registered
2026-03-13
Start date
2025-04-19
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

chronic low back pain

Interventions

chronic low back pain, control group:Conventional rehabilitation therapy (including physiotherapy such as magnetothermal therapy and medium-frequency electrotherapy, as well as conventional exercise t
chronic low back pain,observation group:Conventional rehabilitation therapy+Lumbar Three Needles

Sponsors

Renhe Hospital affiliated of Three Gorges University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: 1)Aged between 18 and 59 years old. 2)Pain localized to the area between below the 12th rib and above the gluteal region. 3)Persistent chronic or recurrent low back pain for more than 3 months, with at least one episode of recurrent pain in the past 3–12 months. 4)Right-handed. 5)Visual Analogue Scale (VAS) score = 3.

Exclusion criteria

Exclusion criteria: 1) History of pelvic or spinal surgery within the past two years; 2) Presence of any specific lumbar pathological changes (e.g., spinal tumours, vertebral fractures, lumbar spinal stenosis, lumbar spondylolisthesis, rheumatoid arthritis, joint stiffness) and severe or progressive scoliosis; 3) Presence of radicular symptoms or neuralgia radiating to both lower limbs; 4) Body Mass Index (BMI) exceeding 30 kg/m²; 5) Undergoing treatment for other types of low back pain within the preceding three months; 6) Recent or anticipated pregnancy; 7) Severe functional impairment of vital organs (e.g., heart, lungs, kidneys); 8) Significant visual or auditory impairment; 9) Cognitive or psychological disorders.

Design outcomes

Primary

MeasureTime frame
Musculoskeletal Ultrasound Acquisition;fNIRS Signal Acquisition;Center of Pressure (COP) Data Acquisition;Surface Electromyography (sEMG) signals (for anticipatory and compensatory postural adjustments, etc.);

Secondary

MeasureTime frame
Rating of Perceived Exertion (RPE);Visual Analogue Scale (VAS);Pain Self-Efficacy Questionnaire (PSEQ);Pain Catastrophizing Scale (PCS);Roland-Morris Disability Questionnaire (RMDQ);Fear-Avoidance Beliefs Questionnaire (FABQ);

Countries

China

Contacts

Public ContactWenwu Xiao

Renhe Hospital affiliated of Three Gorges University

314347250@qq.com+86 188 2727 0822

Outcome results

None listed

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