What this study is
Eligible participants are those who are members of the general surgery residency pediatric gastroenterology fellowship, and adult gastroenterology fellowship. Through a randomized-controlled trial, participants will fill out a baseline set of demographic information including year of training, approximate number of colonoscopies to date, specialty, age, sex and handedness. Participation in this activity is completely voluntary. Trainees will be randomized to one of two groups. Either first participating in an unassisted colonoscopy module twice and then taking a questionnaire and then transitioning to a supervised/coached colonoscopy module session twice and taking a questionnaire, versus the reverse, in which the participant first partakes in a supervised/coached colonoscopy module session twice and then transitions to performing a colonoscopy module twice, unassisted. Objective measures will be assessed by the module software and supervising faculty. Specifically, using individuals' survey responses to see if early supervision improves survey scores. Survey questions focus on student learning, completing module objectives and faculty performance in simulation. The survey will also ask subjects to self-rate their scores and comfort level with endoscopy skills. Survey responses will not be linked to an individuals' performance in their program training and endoscopy coaches will not be made aware of the survey responses.
What's being tested
- Supervision/Coaching
Intervention · BEHAVIORAL
Supervision involves coaching the trainee on insertion and withdrawal technique in a standard colonoscopy in a novice trainee
Study details
- Official title
- Simbionix GI Mentor Simulated Endoscopy Training
- Sponsor
- University of Oklahoma
- Conditions
- Impact of Supervision on Endoscopy Simulation Curriculum
- Enrolling
- 50 people
- Starts
- 2018-03-06
- Est. completion
- 2026-12
- Design
- Single-blind, randomized, parallel groups
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 22 Years – 50 YearsSex ALLHealthy volunteers AcceptedYou may qualify if
- Consenting trainees of adult and pediatric gastroenterology fellowships and general surgery residencies at the University of Oklahoma Health Sciences Center.
You can't join if
- Unwilling to consent.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openUniversity of Oklahoma
Oklahoma City, Oklahoma, United States
- Samantha Harbert · Contact405-271-2045Samantha-Harbert@ouhsc.edu
Recruiting
Study team
Sponsor
University of Oklahoma
Study ID 8244Exempt
Principal investigator
William Tierney, MD
University of Oklahoma
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.