Impact of an e-learning on the Proximal Serrated Polyp Detection Rate

Completed

• Conditions: Colorectal serrated polyps

• Registration Number: NL-OMON21633
• Lead Sponsor: one

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 20

Inclusion Criteria

•Colonoscopies/patients eligible for inclusion:
oScreening & surveillance colonoscopies performed by staff or fellows in average-risk individuals
oColonoscopies by fellows under staff supervision are eligble for inclusion if the supervising staff member was present throughout the procedure.

•Colonoscopists are eligible for inclusion if they:
oPerform at least 20 colonoscopies per month in the ambulatory surgical center
oAre staff GI and Colorectal surgeons with privileges to perform colonoscopy at Mayo Clinic Florida

Exclusion Criteria

•Colonoscopies/patients that will be excluded:
oPatients with known IBD or hereditary polyposis
oPatients with colectomy in their medical history
oPoor bowel preperation and/or incomplete procedure
oColonoscopies with acute indication (e.g. GI-bleed)
oPrior colonoscopy in the past 3 years.
oColonoscopies performed by fellows under staff supervision but in the absence of the supervising staff member

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Improvement in proximal serrated polyp detection rate (PSPDR)

Secondary Outcome Measures

Name	Time	Method
1) Improvement in detectionrate of other polyp subtypes (eg, adenomas, advanced adenomas, hyperplastic polyps). <br>2) Association between endoscopist characteristics & PSPDR improvement