Menu
Not yet recruiting NCT07687992

Application of a Responsive Web-Based Sinus CT Scan Interpretation Training System in Clinical Education

No phase Interventional Education Diagnostic Imaging Otolaryngology Anatomy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Web-Based Interactive Group, Traditional Teaching Group.
Who it may be relevant to
Registry conditions: Education, Diagnostic Imaging, Otolaryngology, Anatomy. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Application of a Responsive Web-Based Sinus CT Scan Interpretation Training System in Clinical Education: A Prospective, Randomized Controlled Trial

Overview

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.

Interventions

  • Other Web-Based Interactive Group
    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.
  • Other Traditional Teaching Group
    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.

Primary outcome measures

  • Objective CT interpretation test score [Time frame: at Day 7]

Eligibility criteria

Inclusion criteria

  • 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.

Exclusion criteria

  • 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).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07687992 · nasalCTscanteaching

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗