Improving Ergonomics in the Operating Room
Simulation for Operating Room Ergonomics - The SORE Study: Creating an Inter-disciplinary Simulation Curriculum for Operating Room Ergonomics
Sunnybrook Health Sciences Centre · NCT05541354
This study is trying to see if teaching operating room teams better ergonomic practices can help reduce their injuries and improve their work experience.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 28 (estimated) |
| Sex | All |
| Sponsor | Sunnybrook Health Sciences Centre (other) |
| Locations | 1 site (Toronto) |
| Trial ID | NCT05541354 on ClinicalTrials.gov |
What this trial studies
This study focuses on assessing the ergonomic needs of operating room (OR) teams, including surgeons, anesthesiologists, and nurses, to develop an educational simulation curriculum aimed at improving ergonomic practices. It addresses the high rates of occupational injuries and discomfort experienced by OR staff due to poor ergonomic management. By bridging the gap between knowledge and application of ergonomic solutions, the study aims to enhance the quality of life for OR staff and reduce the risk of errors and complications during procedures. The approach emphasizes teamwork and communication in implementing ergonomic principles in a busy OR environment.
Who should consider this trial
Good fit: Ideal candidates for this study are members of the operating room team, including surgical, anesthesiology, and nursing staff or trainees at Sunnybrook Health Sciences Centre.
Not a fit: Patients who are not part of the operating room team or those who cannot provide informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this initiative could significantly reduce occupational injuries among OR staff, improving their quality of life and patient safety.
How similar studies have performed: While ergonomic interventions have been proven effective in other settings, this study's focus on a comprehensive educational simulation for OR teams is a novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Member of an OR team (surgery, anesthesiology or nursing staff or trainee) at Sunnybrook Health Sciences Centre Exclusion Criteria: * Lack of informed consent
Where this trial is running
Toronto
- Sunnybrook Research Institute — Toronto, Canada (RECRUITING)
Study contacts
- Study coordinator: Fahad Alam, MSc, MD
- Email: fahad.alam@sunnybrook.ca
- Phone: 416-480-4864
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: Occupational Injuries, Ergonomics, Simulation, Medical Education