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Observational study of preventive effects of locomotive syndrome by treating osteoporosis

Not Applicable
Recruiting
Conditions
Primary osteoporosis
Osteoporosis
D010024
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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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