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

2. juli 2026 oppdatert av: Yanran Huang, First Affiliated Hospital, Sun Yat-Sen University

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.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

36

Fase

  • Ikke aktuelt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Beskrivelse

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).

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
Aktiv komparator: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Objective CT interpretation test score
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. august 2026

Primær fullføring (Antatt)

30. september 2026

Studiet fullført (Antatt)

30. september 2026

Datoer for studieregistrering

Først innsendt

15. juni 2026

Først innsendt som oppfylte QC-kriteriene

2. juli 2026

Først lagt ut (Faktiske)

7. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

7. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

2. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • nasalCTscanteaching

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

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.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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