Evaluating the impact of supervision on endoscopy training
Simbionix GI Mentor Simulated Endoscopy Training
This study is testing how different levels of supervision during training affect how well gastroenterology fellows and general surgery residents learn to perform colonoscopies.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 22 Years to 50 Years |
| Sex | All |
| Sponsor | University of Oklahoma Academic / other |
| Locations | 1 site (Oklahoma City, Oklahoma) |
| Trial ID | NCT03495141 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates how different levels of supervision affect the training of gastroenterology fellows and general surgery residents in performing colonoscopies. Participants will be randomly assigned to either start with unassisted colonoscopy modules followed by supervised sessions or vice versa. Data will be collected through questionnaires and objective measures from the simulation software to assess the training experience and performance. The study aims to enhance the effectiveness of endoscopy training programs.
Who should consider this trial
Good fit: Ideal candidates for this study are trainees in adult and pediatric gastroenterology fellowships and general surgery residencies at the University of Oklahoma.
Not a fit: Patients who are not enrolled in the specified training programs or unwilling to consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve training methods for gastroenterology fellows, leading to better clinical outcomes in patient care.
How similar studies have performed: While there may be studies on simulation training in medical education, this specific approach to comparing supervised versus unassisted training in endoscopy is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Consenting trainees of adult and pediatric gastroenterology fellowships and general surgery residencies at the University of Oklahoma Health Sciences Center. Exclusion Criteria: * Unwilling to consent.
Where this trial is running
Oklahoma City, Oklahoma
- University of Oklahoma — Oklahoma City, Oklahoma, United States (Recruiting)
Study contacts
- Principal investigator: William Tierney, MD — University of Oklahoma
- Study coordinator: William Tierney, MD
- Email: William-Tierney@ouhsc.edu
- Phone: 405-271-5428
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.