RESTORE: REducing Future fractureS and Improving ouTcOmes of fRagility fracturE (NCT06455085)
🩺 Plain-English Summary (8th-Grade Level)
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 join: Review the eligibility criteria below.
Location: University of Alabama at Birmingham — Birmingham, Alabama
Age range: 50 Years
🧪 Interventions in This Study
- Augmented-Fracture Liaison Service Arm (BEHAVIORAL)
- Enhanced Usual Care Arm (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (23 Sites)
- University of Alabama at Birmingham — Birmingham, Alabama
- Mayo Clinic Arizona — Scottsdale, Arizona
- UAMS Health — North Little Rock, Arkansas
- University of Florida- Gainesville — Gainesville, Florida
- University of Florida- Jacksonville — Jacksonville, Florida
- Emory University — Atlanta, Georgia
- Rush University Medical Center — Chicago, Illinois
- University of Illinois Chicago (UIC), UI Health — Chicago, Illinois
- Loyola University Chicago — Maywood, Illinois
- University of Iowa — Iowa City, Iowa
- Allina Health Orthopedics/NorthStar Trauma Network — Coon Rapids, Minnesota
- Missouri Orthopaedic Institute — Columbia, Missouri
- Washington University in St. Louis — St Louis, Missouri
- University of Nebraska Medical Center — Omaha, Nebraska
- Dartmouth-Hitchcock Clinic — Lebanon, New Hampshire
- Hospital for Special Surgery — New York, New York
- Montefiore Medical Center — The Bronx, New York
- The University of North Carolina at Chapel Hill — Chapel Hill, North Carolina
- Duke University — Durham, North Carolina
- Wake Forest University Health Sciences — Winston-Salem, North Carolina
- The Ohio State University — Columbus, Ohio
- Vanderbilt University Medical Center — Nashville, Tennessee
- UT Health Houston — Houston, Texas
📞 Contact the Study Coordinator
Phone: (205) 996-5025
Email: emmills@uabmc.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.