NCT07401004

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

87
On Track

Trial Health Score

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

Enrollment
65

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Dec 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
3 months until next milestone

Study Start

First participant enrolled

December 20, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 27, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 27, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

February 10, 2026

Completed
Last Updated

February 10, 2026

Status Verified

February 1, 2026

Enrollment Period

1 month

First QC Date

September 8, 2025

Last Update Submit

February 5, 2026

Conditions

Keywords

BlinkColorectal PolypsOptical Diagnosis

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

EXPERIMENTAL

Medical 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.

Behavioral: Blink Features Training Video

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.

Single Arm: Blink Features Training

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Colorectal Neoplasms

Condition Hierarchy (Ancestors)

Intestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal DiseasesRectal Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Model Details: Single group of medical students/non-GI trainee's will complete a pre-intervention assessment of colorectal polyp images, receive a brief educational intervention (2-minute Blink features video), and then complete a post-intervention assessment using the same images again.
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

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

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.

Locations