Impact of AI on Trainee ADR

Not Applicable

Recruiting

• Conditions: Adenoma; Adenoma Colon; Colorectal Cancer
• Interventions: Other: Non-AI use Standard of Care endoscopy room; Diagnostic Test: AI use in Endoscopy Room

• Registration Number: NCT05423964
• Lead Sponsor: University of Southern California

Brief Summary

Adenoma detection rate (ADR) is a validated quality metric for colonoscopy with higher ADR correlated with improved colorectal cancer outcomes. Artificial intelligence (AI) can automatically detect polyps on the video monitor which may allow endoscopists in training to improve their ADR. Objective and Purpose of the study: Measure the effect of AI in a prospective, randomized manner to determine its impact on ADR of Gastroenterology trainees.

Detailed Description

Our objective is to determine the impact of AI on the adenoma detection rate of Gastroenterology trainees. The secondary aim of this quality improvement study is to determine the impact of AI based endoscopy on the rate of recording of quality improvement metrics versus historical performance in our program.

Fellows will undergo educational session prior to the start of study, describing commonly used metrics for assessing quality of colonoscopy and how to use the artificial intelligence software. Gastroenterology fellows will be consented for the study prior to initiation. The fellows will be randomized on a daily basis to perform colonoscopies in a room. Outcomes will measure the effects of AI in fellows

Study Timeline

• Study First Submitted: 2022-04-26
• Study First Submitted QC: 2022-06-14
• Study First Posted: 2022-06-21
• Study Start: 2023-01-01
• Status Verified: 2023-03
• Last Update Submitted: 2023-03-02
• Last Update Posted: 2023-03-06
• Primary Completion: 2025-06
• Study Completion: 2025-09

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

• All Gastroenterology fellows at USC performing Endoscopies will be included in the study.

Exclusion Criteria

• If fellows refuse informed consent they will be excluded.
• Procedures performed in the intensive care unit or the operating room will not be counted toward the study metrics as the AI system will only be available in the endoscopy unit.
• If procedures are performed only by faculty, in which the fellow is not the primary operator, they will not be used for study metrics.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Non-Artificial Intelligence Endoscopy Room	Non-AI use Standard of Care endoscopy room	The fellows will be randomized on a daily basis to perform colonoscopies in a non-AI endoscopy room (standard of care).
Artificial Intelligence Endoscopy Room	AI use in Endoscopy Room	The fellows will be randomized on a daily basis to perform colonoscopies in a room with AI (intervention)

Primary Outcome Measures

Name	Time	Method
Average adenoma detection rate	Throughout study, an average of 2 years	Adenoma detection rate with and without AI

Secondary Outcome Measures

Name	Time	Method
Average of polyps detection rate	Through out study, an average of 2 years	Polyp detection rate with and without AI

Trial Locations

Locations (1)

LAC+USC Medical Center; 🇺🇸 Los Angeles, California, United States