Effect of Blink-Based Training on Cancer Detection in Colorectal Polyp Images by Medical Students/Non GI-trainees
Blink
Assessment of Blink Impression for Cancer Detection in Colorectal Polyps Among Medical Students and Non-GI Trainees: A Pre-Post Intervention Study
1 other identifier
interventional
65
1 country
1
Brief Summary
This study investigates whether a brief educational intervention using Blink features can improve medical students' and non-GI trainees' ability to detect colorectal cancer in static polyp images. Secondary aims include evaluating changes in specificity, confidence, and interobserver agreement, determining which Blink features support accurate detection, and examining the link between the number of features recognized and diagnostic performance. The study will recruit medical students and non-GI trainees without prior training in polyp morphology or endoscopic image interpretation, who will complete an online pre- and post-intervention image-based survey.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 8, 2025
CompletedStudy Start
First participant enrolled
December 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 27, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 27, 2026
CompletedFirst Posted
Study publicly available on registry
February 10, 2026
CompletedFebruary 10, 2026
February 1, 2026
1 month
September 8, 2025
February 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in sensitivity for detection of colorectal cancer in polyp images
Sensitivity will be calculated as the proportion of correctly identified cancerous polyps out of all cancerous polyps presented. Comparison will be made between pre-intervention and post-intervention assessments.
Immediately before and after the educational intervention (within one online survey session, approximately 15-20 minutes).
Secondary Outcomes (5)
Change in specificity for cancer detection
Immediately before and after the educational intervention (single online session, ~15-20 minutes).
Change in self-reported diagnostic confidence
Immediately before and after the educational intervention (same session).
Change in interobserver agreement (Fleiss' kappa)
Immediately before and after the educational intervention (same session).
Correlation between presence of individual Blink features and correct cancer classification
Baseline (pre-intervention) and immediately after the educational intervention (within the same online survey session, ~15-20 minutes).
Correlation between number of Blink features identified and diagnostic accuracy
Immediately after the educational intervention (within the same online survey session, ~15-20 minutes).
Study Arms (1)
Single Arm: Blink Features Training
EXPERIMENTALMedical students and non-GI trainees complete a baseline assessment of colorectal polyp images, receive a brief 2-minute educational video on Blink features, and then complete a post-intervention assessment.
Interventions
A brief (2-minute) educational video introducing six Blink features (fold deformation, extra redness, chicken skin mucosa, depression, spontaneous bleeding, ulceration) to improve recognition of colorectal cancer in large non-pedunculated colorectal polyps.
Eligibility Criteria
You may qualify if:
- Images of large non-pedunculated colorectal polyps (LNPCPs) obtained from patients who have provided informed consent for the anonymous use of polyp images during colonoscopy (EC-2024-200).
- Medical students and non-GI trainees who have provided written informed consent to participate in the study.
You may not qualify if:
- Participants (students or non-GI trainees) with prior experience in endoscopy or polyp detection, or those who do not provide informed consent.
- Images deemed to be of insufficient quality by the principal investigator.
- Patients who do not provide informed consent for image use and data collection.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
UZ Brussel
Jette, Brussels Capital, 1090, Belgium
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Gastroenterology trainee (Arts specialist in opleiding)
Study Record Dates
First Submitted
September 8, 2025
First Posted
February 10, 2026
Study Start
December 20, 2025
Primary Completion
January 27, 2026
Study Completion
January 27, 2026
Last Updated
February 10, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP
- Time Frame
- De-identified IPD and supporting information will be available starting 6 months after publication of the primary results and will remain available for 5 years.
- Access Criteria
- Data will be shared with qualified researchers upon reasonable request and after signing a data access agreement.
De-identified individual participant data (IPD) underlying the reported results will be made available upon reasonable request from qualified researchers after publication of the study results. Data will be shared directly by the principal investigator following a data access agreement