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AI Smart Glasses Feedback for Intubation Training in Medical Students

3 novembre 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

200

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Wei-Hung Chan, MD
  • Numero di telefono: 12546 +886-2-87923311
  • Email: whcken@gmail.com

Luoghi di studio

      • Taipei, Taiwan, 114202
        • Tri-Service General Hospital

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 30 anni (Adulto)

Accetta volontari sani

Sì

Sessi ammissibili allo studio

Tutto

Descrizione

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)

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.

Comparatore attivo: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Agreement Between AI and Faculty Examiner Total Scores on the Intubation OSCE
Lasso di tempo: 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)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Faculty-Rated Intubation OSCE Total Score
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Investigatore principale: Wei-Hung Chan, MD, Tri-Service General Hospital (TSGH)

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 gennaio 2027

Completamento primario (Stimato)

31 dicembre 2028

Completamento dello studio (Stimato)

31 dicembre 2028

Date di iscrizione allo studio

Primo inviato

20 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

20 ottobre 2026

Primo Inserito (Effettivo)

27 ottobre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 novembre 2026

Ultimo verificato

1 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • TSGH-ANES-AIGLASS-2027

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

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.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .