Evaluating a Strategy to Improve Pre-Anesthesia Care Discussions (My Anesthesia Choice-Hip Fracture) (NCT06438640)
Implementation and Evaluation of a Strategy to Improve Pre-Anesthesia Care Discussions (My Anesthesia Choice-Hip Fracture)
🩺 Plain-English Summary (8th-Grade Level)
The objective of this study is to assess the implementation process for and the effectiveness of a quality improvement (QI) strategy to increase shared decision-making around anesthesia options for hip fracture surgery at 6 US hospitals. The QI strategy is to be facilitated by a clinician-administered 1-page bedside conversation aid designed to improve the quality of physician-patient communication, paired with brief clinician training. The evaluation will occur via a stepped wedge, cluster randomized trial to be carried out over a period of 34 months.
Who can join: Review the eligibility criteria below.
Location: University of Florida Gainesville — Gainesville, Florida
Age range: 50 Years
🧪 Interventions in This Study
- My Anesthesia Choice-HF Model (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 (6 Sites)
- University of Florida Gainesville — Gainesville, Florida
- Henry Ford Hospital — Detroit, Michigan
- Dartmouth Hitchcock Medical Center — Lebanon, New Hampshire
- Wake Forest University Baptist Medical Center — Winston-Salem, North Carolina
- Cleveland Clinic-Fairview — Cleveland, Ohio
- Penn Presbyterian Medical Center — Philadelphia, Pennsylvania
📞 Contact the Study Coordinator
Phone: (215) 746-7468
Email: neumanm@pennmedicine.upenn.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.
More studies in Hip Fractures
- The Role of Blood Flow Restriction Therapy in Postoperative Elderly Patients With Hip Fracture — Birmingham, Alabama
- Effect of Tranexamic Acid (TXA) on Reduction of Postoperative Blood Transfusion — Toledo, Ohio
- Endoprosthetic Replacement for Pathological Fractures of the Hip: A 35-year Update — New York, New York
- Go Fit Fast, Recovery Trajectory Using PROMIS®, Linking PROMIS® — Los Angeles, California
- PENG vs Femoral Block for Hip Fracture Analgesia — Manhattan, New York
- Comparison of Cryoablation of Pericapsular Nerve Group (PENG) to Fascia Iliaca Catheter in Patients With a Hip Fracture — Minneapolis, Minnesota
Explore by condition: All Hip Fractures clinical trials
💡 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.