Osteoporosis, Postmenopausal
Conditions
Brief summary
Clinical trial to investigate effect of voluntary upper extremity loading in combination with anabolic osteoporosis therapy.
Interventions
Subjects who are prescribed teriparatide by their healthcare provider may enroll in this study. The study intervention consists of loading one upper extremity. Subjects will be trained on how to perform the upper extremity exercises at home. Subjects will be expected to perform the exercises 3 days per week using one arm, with each session consisting of 100 loading cycles lasting a total of approximately 2 minutes each day.
Sponsors
Study design
Eligibility
Inclusion criteria
* women aged 45+ * postmenopausal * osteoporotic with high risk of fracture
Exclusion criteria
* no significant previous use of bone health modifying treatments
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| radius bone mineral density | 12 month change |