Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06438640 · ClinicalTrials.gov registry record · NA
Evaluating a Strategy to Improve Pre-Anesthesia Care Discussions (My Anesthesia Choice-Hip Fracture)
A NA study of Hip Fractures and Femoral Neck Fractures, sponsored by University of Pennsylvania.
- Recruiting
- Registry status
- NA
- Development phase
- 1,881
- Enrollment target
- 6
- Study locations
NCT06438640: Recruiting NA study of Hip Fractures and Femoral Neck Fractures, sponsored by University of Pennsylvania.
NCT06438640 is a NA study of Hip Fractures and Femoral Neck Fractures that is actively recruiting participants, run by University of Pennsylvania. The registered enrollment target is 1,881 participants, above the 496-participant average among 15 other Hip Fractures trials with a reported enrollment target (279% higher). The trial reports 6 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06438640, a NA study of Hip Fractures and Femoral Neck Fractures, is actively recruiting participants, sponsored by University of Pennsylvania.
- RECRUITING
- Registry status
- NA
- Development phase
- 1,881 participants
- Enrollment target
- 6
- Study locations
Study Summary
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.
Primary Outcome
Reach of the intervention will be assessed as the rate of use of the conversation aid during the active implementation phase at each site among eligible patients during the pre-anesthesia evaluation. Data will be collected during the implementation phase at each site.
Conditions Studied
Interventions
- BEHAVIORAL My Anesthesia Choice-HF Model
Study Locations (6)
Florida
- University of Florida Gainesville - Gainesville
Michigan
- Henry Ford Hospital - Detroit
New Hampshire
- Dartmouth Hitchcock Medical Center - Lebanon
North Carolina
- Wake Forest University Baptist Medical Center - Winston-Salem
Ohio
- Cleveland Clinic-Fairview - Cleveland
Pennsylvania
- Penn Presbyterian Medical Center - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,881 participants |
| Start Date | 2024-08-15 |
| Est. Completion | 2028-06-15 |
| Phase | NA |
What NCT06438640 shows while recruiting
NCT06438640 is an interventional study that assigns participants to a tested intervention. Its 1,881 participants enrollment target places it among the larger protocols in the corpus, above the 496-participant average among 15 other Hip Fractures trials with a reported enrollment target (279% higher).
The record links to 4 conditions, with Hip Fractures appearing as the primary indexed condition, and to 1 intervention - of which My Anesthesia Choice-HF Model is the first listed.
NCT06438640 lists 6 locations in 6 states (Florida, Michigan, New Hampshire).
Frequently Asked Questions
What is clinical trial NCT06438640 about?
NCT06438640 is a clinical study titled "Evaluating a Strategy to Improve Pre-Anesthesia Care Discussions (My Anesthesia Choice-Hip Fracture)". 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-administer...
What is the current status of trial NCT06438640?
This trial is currently recruiting. It is a NA study. The enrollment target is 1,881 participants. The study started on 2024-08-15. Estimated completion is 2028-06-15.
What conditions does trial NCT06438640 study?
This clinical trial studies the following conditions: Hip Fractures, Femoral Neck Fractures, Intertrochanteric Fractures, Subtrochanteric Fractures.
What interventions are being tested in trial NCT06438640?
The interventions under investigation include: My Anesthesia Choice-HF Model (BEHAVIORAL).
Who is sponsoring clinical trial NCT06438640?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06438640 being conducted?
This trial has 6 study locations across Florida, Michigan, New Hampshire, North Carolina, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Hip Fractures
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06438640's enrollment target sits among peer trials
1,881 1st of 15 higher than 15 of 15 other Hip Fractures trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Hip Fractures trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
HIP Fracture Accelerated Surgical TreaTment And Care tracK 2 Trial
RECRUITING · NA
-
Cervical Myelopathy in Hip Fracture Patients
RECRUITING · NA
-
PENG vs Femoral Block for Hip Fracture Analgesia
RECRUITING · NA
-
Evaluating the Efficacy of a Mobile Application in Postoperative Rehabilitation
RECRUITING · NA
-
The Role of Blood Flow Restriction Therapy in Postoperative Elderly Patients With Hip Fracture
ACTIVE NOT RECRUITING · NA
-
Utility of Cortical Bone Tissue Properties in the Assessment of Fracture Risk
ACTIVE NOT RECRUITING · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT05675410 · 1,875 participants · Phase 3
A Study to Compare Standard Therapy to Treat Hodgkin Lymphoma to the Use of Two Drugs, Brentuximab Vedotin and Nivolumab
- NCT06891898 · 1,875 participants
The iLet Experience Study
- NCT07356089 · 1,875 participants
Twiist Postmarket Surveillance Study for Type 1 Diabetes
- NCT07203313 · 1,872 participants · NA
Evaluation of Aim to Play, a User-Friendly Digital Application for Teacher Skills Training and Physical Education Activities for 3-5 Grade Students
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI