Skip to content

Endoscopic Quality Improvement Program

The Effect of an Intensive Endoscopic Quality Improvement Program (EQUIP) on Improved Detection and Classification of Non-polypoid (Flat and Depressed) and Polypoid Colorectal Adenomas. (EQUIP Study)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01415817
Acronym
EQUIP
Enrollment
15
Registered
2011-08-12
Start date
2010-08-31
Completion date
2011-04-30
Last updated
2023-05-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adenomatous Polyps, Colorectal Polyps

Keywords

Quality Improvement, Adenoma Detection Rate, Polyp detection rate, Colonoscopy, Training, Colorectal cancer screening

Brief summary

Effective colorectal cancer (CRC) screening relies on early identification and removal of both polypoid and non-polypoid lesions with neoplastic potential. The investigators hypothesize that an intensive training program designed to enhance both recognition and classification of lesions with neoplastic potential, will result in an increase in non-polypoid adenoma detection in addition to and independent of an increase in overall adenoma detection rates.

Detailed description

Our Endoscopic Quality Improvement Program (EQUIP) was a prospective educational intervention with our staff endoscopist as our study population. The investigators measured adenoma detection rates for a baseline period then randomly assigned half of the endoscopists to undergo EQUIP training. The investigators then examined baseline and post-training study adenoma detection rates (ADR's) for all endoscopist (trained and un-trained) to evaluate the impact of training.

Interventions

Series of two training sessions after the first phase of study followed by monthly feedback.

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Colonoscopies performed at Mayo clinic ambulatory surgical center

Exclusion criteria

* Procedures for the indication of acute GI hemorrhage * Active colitis * Hereditary polyposis syndrome * Inflammatory bowel disease * Incomplete procedures * Procedures with surgically altered anatomy (i.e. prior colectomy) * Poor bowel preparation (Boston Bowel preparation score \<5) were also excluded.

Design outcomes

Primary

MeasureTime frameDescription
Measurement of overall adenoma detection rate1 yearPrimary outcome measures will include overall and per patient adenoma detection rate for polypoid and non polypoid neoplastic lesions.

Secondary

MeasureTime frameDescription
Measurement of total polypectomy rate1 YearSecondary outcomes will include total polypectomy rate (hyperplastic vs. adenoma),
Measurement of colonoscopy time1 YearTotal colonoscopy time and endoscopist acceptance. Variables such as patient demographics and prep quality will be adjusted for.
Endoscopist Acceptance1 YearEnsdoscopist acceptance rate will be measured. Variables such as patient demographics and prep quality will be adjusted for.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026