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Clinical Observation on the Treatment of Chronic Neck, Shoulder, Low Back and Leg Pain by Regulating Tendons and Bonesetting Manipulation

Clinical Observation on the Treatment of Chronic Neck Shoulder Low Back and Leg Pain by Regulating Tendons and Bonesetting Manipulation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000553
Enrollment
Unknown
Registered
2024-10-14
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Chronic neck, shoulder, back and leg pain

Interventions

Treatment Group :Transcutaneous nerve electrical stimulation, intermediate frequency pulse electrical therapy, ultra short wave therapy
Test group:On the basis of the control group andtendon-bone-setting manipulation

Sponsors

The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for chronic neck pain, frozen shoulder, rotator cuff injury, nonspecific lower back pain, osteoarthritis of the knee, patellofemoral syndrome, and ankle sprain for chronic neck, shoulder, and low back pain; (2) Age 18 to 70 years old, disease duration = 3 months; (3) Clear consciousness and good communication skills, able to cooperate with the treatment. (4) Voluntarily participate in the study, willing to cooperate with the treatment and follow-up, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Neck, shoulder, back and leg pain due to specific causes such as fractures, dislocations, tumors and infections; (2) Neck pain with spinal cord symptoms; (3) Localized skin breakdown, skin disease or skin sensory disorders; (4) Those with cognitive impairment and unable to cooperate with treatment; (5) Those with serious primary illnesses, mental illnesses, etc; (6) Pregnant or lactating women; (7) Combined cardiovascular and cerebrovascular system diseases, serious abnormalities of liver and kidney functions, abnormalities of coagulation function, serious abnormalities of electrocardiogram, etc; (8) Do not agree to sign the informed consent for this study.

Design outcomes

Primary

MeasureTime frame
VAS;surface EMG;isokinetic strength;muscle and bone ultrasound;

Secondary

MeasureTime frame
EQ-5D;MRI;SF-36;

Countries

china

Contacts

Public Contactli dongjing

The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine

1425374970@qq.com+86 158 5696 1068

Outcome results

None listed

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