RESTORE: REducing Future fractureS and Improving ouTcOmes of fRagility fracturE
Recruiting
N/A
Interventional Study
Osteoporosis
Osteoporotic Fractures
Fragility Fracture
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 50 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 2,634 (estimated)
- Sponsor
- University of Alabama at Birmingham · Other
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About This Trial
RESTORE tests whether Augmented-FLS, where patients are contacted by a patient navigator (serving as the liaison) and referred to a bone health provider, is better than Enhanced Usual Care, which includes patient and PCP education and activation. We also aim to determine the influence of age, race, ethnicity, sex, poverty level, geographic region, and timing of entry into the trial after a fractur…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age 50 years and older (no upper age limit)
* Sustained a primary fragility fracture (hip/femur, pelvis, clinical spine, humerus, wrist) in the last 12 months
* Participant must self-identify a regular primary care provider (PCP)
* Participant must provide a mailing address
* …
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