Application of a Responsive Web-Based Sinus CT Scan Interpretation Training System in Clinical Education
1 other identifier
interventional
36
0 countries
N/A
Brief Summary
The complex anatomy of the paranasal sinuses and skull base presents a steep learning curve for junior clinicians in otolaryngology. This prospective, randomized controlled trial aims to evaluate the effectiveness of a novel, responsive web-based sinus CT scan interpretation training system compared to traditional educational methods. The study will enroll 36 medical trainees and junior resident physicians with no prior specialized training in otolaryngology imaging. Following a standardized baseline video lecture, participants will be randomized (1:1) into two groups for a one-week rotation period. The intervention group will utilize an interactive, cross-platform web system featuring multi-planar correlations, the CLOSE mnemonic guided reading, and case-based self-assessments. The control group will study using standard digitized text-and-image guidelines and clinical consensus documents. The primary outcome is the objective CT interpretation score, which evaluates the accuracy of identifying anatomical variations and pathological grading (e.g., Lund-Mackay score, osteitis grading) across 10 anonymized clinical cases. Secondary outcomes include interpretation time, diagnostic confidence, and system usability. The findings of this study will provide valuable evidence on whether interactive digital tools can effectively accelerate the learning curve and improve diagnostic accuracy in specialized medical imaging education.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2026
Shorter than P25 for not_applicable
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
June 15, 2026
CompletedFirst Posted
Study publicly available on registry
July 7, 2026
CompletedStudy Start
First participant enrolled
August 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 30, 2026
July 7, 2026
July 1, 2026
2 months
June 15, 2026
July 2, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Objective CT interpretation test score
The objective CT interpretation test includes 10 anonymized clinical CT sequences. Participants must independently identify anatomical variations (e.g., Onodi cells, Haller cells, ostiomeatal complex) and complete the Lund-Mackay staging and osteitis grading. The total test score ranges from 0 to 100 points. A higher score indicates higher diagnostic accuracy and better performance in CT interpretation.
at Day 7
Study Arms (2)
Web-Based Interactive Training Group
EXPERIMENTALWeb-Based Interactive Training
Traditional Multimedia Learning Group
ACTIVE COMPARATORTraditional Multimedia Learning
Interventions
Following the exact same standardized baseline lecture video on sinus anatomy, participants will receive a digitized traditional teaching material package for self-directed learning over a 1-week rotation period. This standard educational package includes detailed text-and-image handouts on sinus anatomy and static CT evaluation criteria derived from the official clinical expert consensus guidelines.
In addition to watching the baseline video, participants will receive a standard digitized traditional teaching material package (including detailed text-and-image handouts on sinus anatomy and the CT evaluation standard documents from the "Expert Consensus on the Diagnosis and Treatment of Chronic Rhinosinusitis"). Participants are required to complete self-directed reinforcement learning using these materials within the same period.
Eligibility Criteria
You may qualify if:
- Medical students currently in their clinical clerkship or internship phase, or junior physicians currently undergoing standardized residency training;
- No prior systematic training in specialized otolaryngology-head and neck surgery (ORL-HNS) imaging;
- Voluntary participation in the study with a signed informed consent form.
You may not qualify if:
- Inability to access a basic smartphone or computer required for the digital training system;
- Anticipated inability to complete the intervention, and assessment period (e.g., due to planned prolonged leave of absence).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr.
Study Record Dates
First Submitted
June 15, 2026
First Posted
July 7, 2026
Study Start
August 1, 2026
Primary Completion (Estimated)
September 30, 2026
Study Completion (Estimated)
September 30, 2026
Last Updated
July 7, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share
Individual participant data (IPD) will not be shared publicly. Due to the specific nature of the study population (a small cohort of clinical rotators in a single department) and the relatively small sample size, sharing raw IPD poses a significant risk of indirect re-identification. Furthermore, the informed consent obtained from the participants strictly limits data access to the immediate research team to protect their academic and professional privacy. Aggregate data and statistical analyses will be reported in published manuscripts.