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Efficacy of tendon acupuncture at Myofascial Trigger Points Combined with Core Stability Training for the Treatment of Non-Specific Low Back Pain

Efficacy of tendon acupuncture at Myofascial Trigger Points Combined with Core Stability Training for the Treatment of Non-Specific Low Back Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000095
Enrollment
Unknown
Registered
2026-01-17
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Nonspecific lower back pain

Interventions

Control group: lumbar traction + medium-frequency therapy + core stability training.:Lumbar Traction: The patient relaxes and assumes a supine position for traction. The traction weight is primarily b

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: Meet the diagnostic criteria for Non-Specific Low Back Pain (NSLBP) and the syndrome differentiation criteria for Liver-Kidney Deficiency as outlined in the *Chinese Expert Consensus on Diagnosis and Management of Acute/Chronic Non-Specific Low Back Pain (2016)* by the Expert Group of the Spine and Spinal Cord Committee, Chinese Association of Rehabilitation Medicine. 2: Age between 18 and 60 years (inclusive). 3: Visual Analog Scale (VAS) score = 6 points. 4: No prior receipt of the treatment interventions used in this study within the past month. 5: No frequent use of analgesic medication (defined as = 4 days per week). 6: Absence of medications or diseases affecting muscle metabolism (e.g., glucocorticoid therapy). 7: Normal hearing and psychological status, with good compliance and cooperation. 8: Voluntary participation in this study with provision of signed informed consent.

Exclusion criteria

Exclusion criteria: 1: Vulnerable populations, including individuals with mental illness, cognitive impairment, pregnant women, and illiterate persons. 2: Presence of severe underlying cardiovascular, hepatic, or renal diseases. 3: Comorbidities that significantly affect activities of daily living, such as osteoarthritis, gout, malignant tumors, or acute trauma/fractures. 4: History of spinal surgery. 5: Severe needle phobia. 6: Concurrent participation in other clinical trials involving interventions for NLBP patients.

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale (VAS);RMDQ(Roland Morris Disability Questionnaire);

Secondary

MeasureTime frame
Surface Electromyography Technology;The Oswestry Disability Index (ODI);Joint Position Sense (JPS) Test;

Countries

China

Contacts

Public ContactLi yongzhong

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine

liyongzhong1989@163.com0571-86006054

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 7, 2026