Education after orthopedic trauma surgery
Validating a "Teach-back" Protocol to Improve Recall in Orthopedic Trauma Patients
NA · University Hospitals Cleveland Medical Center · NCT05616312
This study tests if giving patients information about their pelvic and leg injuries after surgery helps them remember important details, follow treatment advice, and feel more satisfied with their care.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 216 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | University Hospitals Cleveland Medical Center (other) |
| Locations | 1 site (Cleveland, Ohio) |
| Trial ID | NCT05616312 on ClinicalTrials.gov |
What this trial studies
This study evaluates the impact of educational interventions on patients who have undergone trauma surgeries for isolated fractures of the pelvis and lower extremities. Participants will be divided into two groups: one receiving educational information about their injury and treatment, and the other not receiving such education. The study aims to assess how this education affects patients' recall of information, adherence to treatment recommendations, and overall satisfaction with their care.
Who should consider this trial
Good fit: Ideal candidates are individuals who have undergone surgical treatment for isolated fractures of the pelvis or lower extremities.
Not a fit: Patients with cognitive impairments or those receiving orthopedic care at another institution may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance patient understanding and compliance, leading to better recovery outcomes.
How similar studies have performed: While the specific approach of this study may be novel, educational interventions in healthcare have shown promise in improving patient outcomes in similar contexts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Isolated open or closed fracture of the pelvis and/or lower extremity treated surgically Exclusion Criteria: * Patient receiving orthopedic care or follow-up at another institution * Non-English speaking * Incarcerated (or likely impending incarceration) * Currently enrolled in a study that does not permit co-enrollment * Traumatic brain injury, dementia, or other cognitive impairment
Where this trial is running
Cleveland, Ohio
- University Hospitals Cleveland Medical Center — Cleveland, Ohio, United States (RECRUITING)
Study contacts
- Principal investigator: John Sontich, MD — University Hospitals Cleveland Medical Center
- Study coordinator: Kallie J Chen, MD
- Email: kallie.chen@uhhospitals.org
- Phone: 920-912-6244
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Education After Trauma