Skip to content

Study on the Effects and Mechanism of Neuromuscular Electrical Stimulation Combined with Training on Delayed Activation of Core Muscle Groups in Patients with Non-Specific Low Back Pain

Study on the Effects and Mechanism of Neuromuscular Electrical Stimulation Combined with Training on Delayed Activation of Core Muscle Groups in Patients with Non-Specific Low Back Pain

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092409
Enrollment
Unknown
Registered
2024-11-15
Start date
2025-01-01
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Non-specific low back pain

Interventions

Synchronized intervention group:Neuromuscular electrical stimulation was performed simultaneously with core training
Non-synchronous intervention group:Neuromuscular electrical stimulation was administered prior to core training
Sham stimulation intervention group:Sham neuromuscular electrical stimulation was performed simultaneously with core training

Sponsors

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Age between 18 and 60 years. (2) Meets the diagnostic and treatment criteria for CNLBP as outlined in the "2016 Expert Consensus on Diagnosis and Treatment of Acute/Chronic Non-Specific Low Back Pain in China" by the Spine and Spinal Cord Committee of the Chinese Association of Rehabilitation Medicine. (3) Visual Analog Scale (VAS) score <=6. (4) Has not received the treatment interventions used in this study in the past month. (5) Does not frequently use analgesics (less than 4 days per week). (6) No medication or disease affecting muscle metabolism (e.g., glucocorticoids). (7) Normal hearing and psychological condition with high compliance. (8) Willing to participate in this study and has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Vulnerable populations, including individuals with mental illness, cognitive impairment, critical conditions, minors, pregnant women, and illiterate individuals. 2. Participants with severe underlying diseases, such as cardiovascular, cerebrovascular, liver, or kidney conditions. 3. Participants with conditions affecting daily living abilities, including osteoarthritis, gout, tumors, acute trauma, or fractures. 4. History of spinal surgery. 5. Contraindications for NMES, such as pacemakers, edema, sensory abnormalities, or thromboembolism. 6. Participants currently enrolled in other clinical trials for interventions in CNLBP (Chronic Non-Specific Low Back Pain).

Design outcomes

Primary

MeasureTime frame
Surface Electromyography (sEMG);

Secondary

MeasureTime frame
the Visual Analog Scale;The Oswestry Disability Index (ODI);Transverse Abdominis Thickness;Proprioception Testing;Multifidus Muscle Thickness;Multifidus Muscle Cross-Sectional Area;

Countries

China

Contacts

Public ContactLi Yongzhong

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine

liyongzhong1989@163.com+86 158 6917 3168

Outcome results

None listed

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