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Exploring the Clinical Efficacy of Kinesiology Tape on Chronic Non-Specific Low Back Pain Based on Surface Electromyography Sticking Methods

Exploring the Clinical Efficacy of Kinesiology Tape on Chronic Non-Specific Low Back Pain Based on Surface Electromyography Sticking Methods

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099445
Enrollment
Unknown
Registered
2025-03-24
Start date
2022-01-03
Completion date
Unknown
Last updated
2025-03-31

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

Control Group:Conventional Rehabilitation Training
Treatment Group A:Treat the lumbar area with intramuscular taping in a cross pattern.
Treatment Group B:Transdermal acupressure patches are applied in a cross-shaped manner to the painful local area for treatment.
Treatment Group C:Based on objective indicators of asymmetric spinal muscle activity in patients with nonspecific low back pain, four pieces of type I kinesiology tape were used for taping interventio

Sponsors

Dongnan University Affiliated Zhongda Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients met the diagnostic criteria for chronic nonspecific low back pain, aged between 18 and 60 years, with a disease course of at least 3 months, and VAS score <7. 2. The pain was localized or diffusely unclear, accompanied by buttock or posterior lateral thigh pain, but did not extend below the knee joint, and the straight leg raising test was negative (-). 3. No abnormalities were found in the sensory, reflex, and muscle strength of both lower extremities. 4. Radiography, CT, or MRI of the lumbar spine showed no abnormalities./

Exclusion criteria

Exclusion criteria: 1. Those who cannot tolerate rehabilitation training or are allergic to kinesiology tape; 2. Patients with severe spinal diseases, including spinal fractures, lumbar spondylolisthesis, tumors, tuberculosis, infections, etc.; 3. Patients with severe lumbar stenosis, nucleus pulposus prolapse, or severe cauda equina syndrome, with nerve compression symptoms and signs in lumbar disc herniation; 4. Pregnant women; 5. Patients with ankylosing spondylitis or rheumatoid arthritis; 6. Patients with severely impaired or failing functions of vital organs such as the heart, lungs, liver, and kidneys; 7. Participants who cannot complete the experimental movements according to requirements, or those who voluntarily request withdrawal from the study, or serious adverse events occur during the trial.

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale;

Secondary

MeasureTime frame
ODI Lumbar Function Index;Surface Electromyography;Body Center of Gravity Offset Index;Elastic modulus value of the lumbar muscles;Back muscle fatigue test time;

Countries

China

Contacts

Public ContactFan Youqiang

Dongnan University Affiliated Zhongda Hospital

fly_2580@163.com+86 139 1397 5953

Outcome results

None listed

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