neck and shoulder pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Age 18 to 65 years, regardless of gender. (2) Clearly diagnosed with neck and shoulder pain, accompanied by symptoms such as pain, stiffness, and limited range of motion in the neck and shoulder area. (3) Informed consent to this study, voluntarily agree to participate and sign the informed consent form. (4) No use of other pain treatment medications or physical therapy methods within 24 hours prior to treatment. Volunteers who meet the above criteria and have read and signed the informed consent form may be included.
Exclusion criteria
Exclusion criteria: (1) Individuals under 18 years of age or over 65 years of age. (2) Individuals with other serious primary diseases. (3) Individuals allergic to the components of the far-infrared tendon-soothing and blood-activating plaster. (4) Patients with malignant tumors, pregnant women, angina patients, and children. (5) Patients with severe heart, liver, kidney, or lung failure are contraindicated. (6) Individuals with open wounds at the treatment site. (7) Individuals unable to cooperate with the completion of treatment and evaluation. Individuals meeting any of the above criteria will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS;NDI; | — |
Countries
China
Contacts
Fuzhou University Affiliated Provincial Hospital