chronic nonspecific neck pain
Conditions
Interventions
Case group:None
Control group:None
Sponsors
Zhujaing hospital, Southern Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 55 Years
Inclusion criteria
Inclusion criteria: Experimental group: ? aged between 18 and 55 years ? Chronic nonspecific neck pain for at least 3 months ? NPRS pain score > 3 points ? Volunteer to participate in the trial and sign the informed consent form ? Literacy and ability to understand the test. Control group: ? Age between 18 and 55 years old ? No history of neck pain ? Voluntarily participate in the trial and sign the informed consent ?Literacy and ability to understand the test.
Exclusion criteria
Exclusion criteria: Experimental group: ? have other congenital or known musculoskeletal, neuromuscular, neurological, endocrine, psychiatric, infectious, traumatic diseases (psychiatric disorders, history of cancer, pregnancy, disc prolapse, spondylolisthesis, vertebral fractures, spinal stenosis, arthritis, osteoporosis, systemic rheumatoid disease, thoracic outlet syndrome, severe night pain, specific pathological conditions (such as signs of infection), and other musculoskeletal disorders affecting the cervical region, neck trauma within 48 hours) ? Can't complete the movement of the neck in all directions ? Other situations that the researchers judged to be unsuitable for inclusion. Control group: ? has other congenital or known musculoskeletal, neuromuscular, neurological, endocrine, psychiatric, infectious, traumatic diseases (psychiatric disorders, cancer history, pregnancy, disc prolapse, spondylolisthesis, vertebral fractures, spinal stenosis, arthritis, osteoporosis, systemic rheumatoid disease, thoracic outlet syndrome, severe night pain, specific pathological conditions (such as signs of infection), and other musculoskeletal disorders affecting the neck region, neck trauma within 48 hours) ? Can't complete the movement of the neck in all directions ? Other situations that the researchers judged to be unsuitable for inclusion.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cervical load;muscle co-activation ratio; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain intensity;dysfunction;life quality;Psychological indicators;Muscle indicators; | — |
Countries
China
Contacts
Public ContactGuozhi Huang
Zhujiang hospital,Southern Medical University
Outcome results
None listed