osteogenesis imperfecta
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who went to the Pediatric Orthopedics Department of Shenzhen Hospital of the University of Hong Kong; 2. Conscious and able to communicate clearly; 3. Age and gender are not limited; 4. Subjects and their guardians (or their guardians) voluntarily participate in this clinical trial and have signed a written informed consent form; 5. Have accurate contact information.
Exclusion criteria
Exclusion criteria: 1. No diagnosis of osteogenesis imperfecta 2. No surgical treatment in this hospital 3. No accurate and feasible contact information; 4. Unable to communicate or having no relatives can communicate instead of the patient.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional Movement Screen(FMS) ;Patient-Reported Outcomes Measurement Information System(PROMIS); | — |
Secondary
| Measure | Time frame |
|---|---|
| Bone Mineral Density(BMD); | — |
Countries
China
Contacts
Shenzhen Hospital of the University of Hong Kong