NCT06577610

Brief Summary

The goal of this clinical trial is to learn if colonoscopy monitoring program works to adenoma detection rate in endoscopists. It will also learn about the impact on sessile serrated lesion detection rate, adenomas per colonoscopy, sessile serrated lesions per colonoscopy, advanced adenoma detection rate. The main questions it aims to answer are: Does colonoscopy monitoring program effect on adenoma detection rate in endoscopists? Participants will: Receive result of colonoscopy monitoring program or not every 3 months for 1 year

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2024

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 27, 2024

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 29, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

October 1, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2025

Completed
Last Updated

September 19, 2024

Status Verified

September 1, 2024

Enrollment Period

1 year

First QC Date

August 27, 2024

Last Update Submit

September 9, 2024

Conditions

Adenoma Colon PolypSessile Serrated Adenoma

Keywords

adenomaSessile Serrated Adenomacolonoscopy

Outcome Measures

Primary Outcomes (1)

  • adenoma detection rate

    the percentage of patients with at least one histologically proven adenoma

    1 year

Secondary Outcomes (4)

  • sessile serrated lesion detection rate

    1 year

  • adenomas per colonoscopy

    1 year

  • sessile serrated lesions per colonoscopy

    1 year

  • advanced adenoma detection rate

    1 year

Study Arms (2)

Feedback group

EXPERIMENTAL

The feedback group will be notified of the colonoscopy performances.

Behavioral: Feedback from colonoscopy monitoring program

Control group

NO INTERVENTION

The control group will not be notified of the colonoscopy performances.

Interventions

Feedback from colonoscopy monitoring programBEHAVIORAL

Adenoma detection rate feedback from colonoscopy monitoring programs

Feedback group

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Endoscopists with at least 1 year of colonoscopy experience

You may not qualify if:

  • Endoscopists with less than 1 year of colonoscopy experience

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Adenoma

Condition Hierarchy (Ancestors)

Neoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasms

Central Study Contacts

Jung Kim

CONTACT

82-10-5195-9531piejung88@naver.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SCREENING
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

August 27, 2024

First Posted

August 29, 2024

Study Start

October 1, 2024

Primary Completion

October 1, 2025

Study Completion

October 1, 2025

Last Updated

September 19, 2024

Record last verified: 2024-09

Data Sharing

IPD Sharing
Will not share