Observational study of preventive effects of locomotive syndrome by treating osteoporosis
Not Applicable
Recruiting
- Conditions
- Primary osteoporosisOsteoporosisD010024
- Registration Number
- JPRN-jRCT1040210025
- Lead Sponsor
- Sobue Naohisa
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
1. Postmenopausal women with osteoporosis
2. Patients who used bisphosphonate and were given the pamphlet of exercise (locomotion training)
3. Written informed consent
Exclusion Criteria
1. Previous romosozumab or denosumab or teriparatide or bisphosphonate use
2. Hypocalcemia
3. Patients judged to be in appropriate for study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method