Application of a Responsive Web-Based Sinus CT Scan Interpretation Training System in Clinical Education
Application of a Responsive Web-Based Sinus CT Scan Interpretation Training System in Clinical Education: A Prospective, Randomized Controlled Trial
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.
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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).
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：他の
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的：Web-Based Interactive Training Group
Web-Based Interactive Training
|
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.
|
|
アクティブコンパレータ：Traditional Multimedia Learning Group
Traditional Multimedia Learning
|
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.
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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Objective CT interpretation test score
時間枠：at Day 7
|
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
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- nasalCTscanteaching
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。