Osteoporosis
Conditions
Interventions
Participants with cervical/shoulder/back pain or lumbosacral/leg pain constitute the intervention group (Participants presenting with characteristic pain patterns including postural pain, positional t
Control group (Participants without the five pain patterns of the experimental group and asymptomatic):None
Sponsors
Xijing Hospital, Air Force Medical University
Eligibility
Sex/Gender
Female
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Participants capable of completing questionnaires, bone density measurements, and quantitative assays for active vitamin D
Exclusion criteria
Exclusion criteria: 1.Individuals with osteomyelitis, bone tumors, metastatic carcinoma, soft tissue sarcomas, limb fractures, or orthopedic diseases requiring surgical intervention; 2.Patients with severe traumatic brain injury or significant cognitive impairment; 3.Subjects presentingneurological deficits necessitating surgical management or requiring neurology consultation for intrinsic nervous system diseases; 4.Other conditions contraindicating participation; 5.Inpatients; 6.Participants or their legal guardians refusing study enrollment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bone mineral density (BMD);Active vitamin D levels; | — |
Countries
China
Contacts
Public ContactZhensheng Ma
Xijing Hospital, Air Force Medical University
Outcome results
None listed