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AI Smart Glasses Feedback for Intubation Training in Medical Students

2026年11月3日 更新者:Wei-Hung Chan、Tri-Service General Hospital (TSGH)

AI Smart Glasses for Automated Scoring and Feedback in Medical Students' Endotracheal Intubation OSCE: A Cluster-Randomized Educational Study

The goal of this educational study is to learn whether AI smart glasses can score and give feedback on endotracheal intubation performed by medical students on a manikin, and when this AI feedback is most useful during anesthesia training. The main questions it aims to answer are:

  • Do AI scores of the intubation OSCE (Objective Structured Clinical Examination) agree with scores given by faculty examiners?
  • Does practicing with AI smart-glasses feedback before or after the airway lecture lead to better intubation OSCE performance, self-efficacy, and cognitive load?

Medical interns rotating through the Department of Anesthesiology at Tri-Service General Hospital (Taiwan) for 2 weeks will be randomized by rotation group to practice intubation once with the AI smart glasses either before the airway lecture (week 1) or after it (week 2). At the end of the rotation, all participants will take an intubation OSCE while wearing the AI glasses, scored independently by a faculty examiner and by the AI. Participants will also complete short questionnaires on self-efficacy (before and after the rotation) and cognitive load (after AI practice). All procedures are performed on a manikin; no patients are involved.

研究概览

详细说明

Background: Endotracheal intubation is one of the core clinical skills required of medical graduates in Taiwan, but intern pass rates in simulated intubation examinations at our hospital are only about 50-60%. Procedural skill learning depends on timely, specific feedback, yet faculty time is limited. AI smart glasses (HTC) record first-person video of the procedure and use artificial intelligence to score it against a standardized checklist and return immediate item-by-item feedback. The agreement between AI and faculty scoring has not been validated, and the optimal timing of AI feedback relative to formal teaching is unknown.

Design: Prospective, single-center, cluster-randomized (by rotation group, 3-4 interns per group), two-arm parallel educational trial. Rotation groups are allocated 1:1 by computer-generated block randomization.

Procedures (2-week anesthesiology rotation):

  • Week 1, Day 1: informed consent and pre-test questionnaire.
  • Arm 1 (AI before lecture): one AI smart-glasses intubation practice on a manikin during Week 1, Days 2-4, with immediate AI scoring and feedback, followed by a cognitive load questionnaire.
  • Week 1, Day 5: airway lecture (about 1 hour) for all interns.
  • Arm 2 (AI after lecture): one AI smart-glasses practice during Week 2, Days 1-4, with immediate AI scoring and feedback, followed by a cognitive load questionnaire.
  • Last day of Week 2: end-of-rotation intubation OSCE (8 minutes) wearing the AI glasses; a faculty examiner scores the performance in person and the AI scores it independently; post-test questionnaire.

The investigator assisting with the glasses does not teach intubation during practice. OSCE faculty examiners are blinded to group allocation and do not see the AI score before completing their own scoring. Examiners are calibrated before enrollment using at least 10 practice videos.

OSCE checklist: 10 items scored 0/1/2 (total 0-20) plus a global rating scored 1 to 5, pass/fail judgment, and intubation time.

Questionnaires: a 4-item intubation-specific self-efficacy scale adapted from a published smart-glasses intubation training study and a 39-item medical learning self-efficacy questionnaire adapted from a validated multi-dimensional instrument for medical students, both rated on 5-point scales; and a validated 10-item cognitive load questionnaire measuring intrinsic, extraneous, and germane load, rated on a 5-point scale.

Statistical analysis: Agreement between AI and faculty total scores will be assessed with ICC(2,1) (two-way random effects, absolute agreement) with 95% CI and Bland-Altman analysis; item-level agreement with quadratic weighted kappa; pass/fail agreement with Cohen's kappa, sensitivity, and specificity. Between-arm comparisons of OSCE performance, self-efficacy change, and cognitive load will use linear or generalized linear mixed-effects models with rotation group as a random effect, following the intention-to-treat principle.

Sample size: 200 interns (about 100 per arm). With an expected ICC of 0.80, this gives a 95% CI width of no more than 0.10 for the primary agreement analysis; allowing 10% attrition and a design effect of about 1.13, it can detect an effect size of about 0.45 between arms in OSCE total score.

研究类型

介入性

注册 (估计的)

200

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Wei-Hung Chan, MD
  • 电话号码:12546 +886-2-87923311
  • 邮箱:whcken@gmail.com

学习地点

      • Taipei、台湾、114202
        • Tri-Service General Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 30年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Medical interns (medical students in the clinical internship year) rotating through the Department of Anesthesiology, Tri-Service General Hospital, during the study period
  • Aged 18 years to 30 years old
  • Voluntarily agree to participate and provide written informed consent

Exclusion Criteria:

  • Unwilling to participate
  • Previously enrolled in this study during an earlier rotation (no repeat enrollment)

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:AI Feedback Before Airway Lecture

Rotation groups randomized to this arm perform one AI smart-glasses intubation practice session on a manikin with immediate AI scoring and feedback during Week 1, Days 2-4 of the 2-week anesthesiology rotation, before the airway lecture (Week 1, Day 5), followed by a cognitive load questionnaire. All participants complete the end-of-rotation intubation OSCE wearing the AI glasses (scored by faculty and AI) and the self-efficacy questionnaires at the start and end of the rotation.

One individual practice session (about 15 minutes) of endotracheal intubation on an airway manikin while wearing AI smart glasses (HTC). The glasses record first-person video of the procedure; after upload, the AI scores the performance against the 10-item intubation OSCE checklist (each item 0/1/2, total 0-20, plus a 1-5 global rating) and immediately displays item-by-item scores and written feedback for the student to review. The investigator only assists with operating the glasses and does not teach intubation during the session. The two arms differ only in the timing of this session relative to the airway lecture.

有源比较器:AI Feedback After Airway Lecture

Rotation groups randomized to this arm attend the airway lecture (Week 1, Day 5) first and then perform one AI smart-glasses intubation practice session on a manikin with immediate AI scoring and feedback during Week 2, Days 1-4 of the 2-week anesthesiology rotation, followed by a cognitive load questionnaire. All participants complete the end-of-rotation intubation OSCE wearing the AI glasses (scored by faculty and AI) and the self-efficacy questionnaires at the start and end of the rotation.

One individual practice session (about 15 minutes) of endotracheal intubation on an airway manikin while wearing AI smart glasses (HTC). The glasses record first-person video of the procedure; after upload, the AI scores the performance against the 10-item intubation OSCE checklist (each item 0/1/2, total 0-20, plus a 1-5 global rating) and immediately displays item-by-item scores and written feedback for the student to review. The investigator only assists with operating the glasses and does not teach intubation during the session. The two arms differ only in the timing of this session relative to the airway lecture.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Agreement Between AI and Faculty Examiner Total Scores on the Intubation OSCE
大体时间:End of the 2-week anesthesiology rotation (Week 2, last day)

Intraclass correlation coefficient ICC(2,1) (two-way random effects, absolute agreement, single rater) with 95% confidence interval between the AI-generated total score and the faculty examiner's total score on the 10-item endotracheal intubation OSCE checklist (each item scored 0, 1, or 2; total score range 0-20, higher scores indicate better performance). Bland-Altman mean difference and 95% limits of agreement will also be reported. The faculty examiner is blinded to group allocation and to the AI score.

End of the 2-week anesthesiology rotation (Week 2, last day)

次要结果测量

结果测量
措施说明
大体时间
Faculty-Rated Intubation OSCE Total Score
大体时间:End of the 2-week anesthesiology rotation (Week 2, last day)

Total score on the 10-item endotracheal intubation OSCE checklist rated by a faculty examiner blinded to group allocation (each item 0, 1, or 2; range 0-20; higher scores indicate better performance), compared between arms.

End of the 2-week anesthesiology rotation (Week 2, last day)
Faculty-Rated Global Performance Rating on the Intubation OSCE
大体时间:End of the 2-week anesthesiology rotation (Week 2, last day)

Faculty examiner's global rating of intubation performance on a 5-point scale (1 = poor, 2 = needs improvement, 3 = fair, 4 = good, 5 = excellent; higher scores indicate better performance), compared between arms.

End of the 2-week anesthesiology rotation (Week 2, last day)
Intubation OSCE Pass Rate
大体时间:End of the 2-week anesthesiology rotation (Week 2, last day)

Percentage of participants judged by the faculty examiner to pass the intubation OSCE according to the national graduation competency standard (correct laryngoscope use, correct and appropriate tube placement, and completion of one tube placement within 30 seconds), compared between arms.

End of the 2-week anesthesiology rotation (Week 2, last day)
Intubation Time
大体时间:End of the 2-week anesthesiology rotation (Week 2, last day)

Time in seconds from insertion of the laryngoscope blade into the mouth to completion of endotracheal tube placement and removal of the laryngoscope, timed by the faculty examiner during the OSCE, compared between arms.

End of the 2-week anesthesiology rotation (Week 2, last day)
Item-Level and Pass/Fail Agreement Between AI and Faculty Examiner
大体时间:End of the 2-week anesthesiology rotation (Week 2, last day)

Agreement between AI and faculty examiner for each of the 10 OSCE checklist items (0/1/2) assessed with quadratic weighted kappa, and for the global rating (scored 1 to 5) assessed with ICC(2,1); agreement on pass/fail assessed with Cohen's kappa, with sensitivity and specificity of the AI pass/fail judgment using the faculty judgment as the reference standard.

End of the 2-week anesthesiology rotation (Week 2, last day)
Change in Intubation-Specific Self-Efficacy Score
大体时间:Baseline (Week 1, Day 1) and end of the 2-week rotation (Week 2, last day, after the OSCE)

Mean score of a 4-item intubation self-efficacy scale adapted from a published smart-glasses intubation training study, each item rated on a 5-point scale (1 = not at all confident, 5 = very confident; range 1-5; higher scores indicate greater self-efficacy). Change from baseline to end of rotation is compared between arms.

Baseline (Week 1, Day 1) and end of the 2-week rotation (Week 2, last day, after the OSCE)
Change in Medical Learning Self-Efficacy Score
大体时间:Baseline (Week 1, Day 1) and end of the 2-week rotation (Week 2, last day, after the OSCE)

Mean score of a 39-item medical learning self-efficacy questionnaire adapted from a validated multi-dimensional medical students' learning self-efficacy questionnaire (subscales: conceptual understanding, practical work, everyday application, higher-order cognitive skills, medical communication, professionalism, and academic self-efficacy), each item rated on a 5-point Likert scale (1 = strongly disagree, 5 = strongly agree; range 1-5; higher scores indicate greater self-efficacy). Change from baseline to end of rotation is compared between arms.

Baseline (Week 1, Day 1) and end of the 2-week rotation (Week 2, last day, after the OSCE)
Cognitive Load During AI Smart-Glasses Practice
大体时间:Immediately after the AI smart-glasses practice session (Week 1, Days 2-4 in Arm 1; Week 2, Days 1-4 in Arm 2)

Intrinsic (items 1-3), extraneous (items 4-6), and germane (items 7-10) cognitive load subscale mean scores on a validated 10-item cognitive load questionnaire, each item rated on a 5-point scale (1 = not at all applicable, 5 = completely applicable; range 1-5). Higher intrinsic and extraneous scores indicate greater load; higher germane scores indicate greater investment in learning. Compared between arms.

Immediately after the AI smart-glasses practice session (Week 1, Days 2-4 in Arm 1; Week 2, Days 1-4 in Arm 2)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Wei-Hung Chan, MD、Tri-Service General Hospital (TSGH)

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2027年1月1日

初级完成 (估计的)

2028年12月31日

研究完成 (估计的)

2028年12月31日

研究注册日期

首次提交

2026年10月20日

首先提交符合 QC 标准的

2026年10月20日

首次发布 (实际的)

2026年10月27日

研究记录更新

最后更新发布 (实际的)

2026年11月6日

上次提交的符合 QC 标准的更新

2026年11月3日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Individual participant data, including first-person procedure videos, will not be shared. The informed consent specifies that study data are accessible only to the principal investigator and authorized co-investigators and that results will be reported only in aggregate. Aggregate results will be published in peer-reviewed journals.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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