EligibleTrials

RESTORE: REducing Future fractureS and Improving ouTcOmes of fRagility fracturE

Recruiting · NCT06455085 · Interventional (participants receive a specific treatment) · Lead sponsor: University of Alabama at Birmingham

View the official record on ClinicalTrials.gov →
Osteoporosis

Interventions studied

Augmented-Fracture Liaison Service ArmEnhanced Usual Care Arm

What this trial is about

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 fracture on the effectiveness of the two strategies.

Who can take part

Age range
50 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

23 locations listed across 16 US states.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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