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Effectiveness of Integrated Multimodal Digital and Specimen-Based Neuroanatomy Teaching Among Medical Students

24. september 2026 oppdatert av: Khin Ei Ei Saw

Effectiveness of Integrated Multimodal Digital and Specimen-Based Neuroanatomy Teaching in Improving Knowledge, Reducing Perceived Learning Difficulty, and Enhancing Confidence Among Medical Students

This three-phase randomized controlled educational intervention trial will evaluate the effectiveness of integrated multimodal digital and specimen-based neuroanatomy teaching compared with traditional specimen-based revision among Medical Year 2 students. The study will assess knowledge, perceived learning difficulty, and confidence in a difficult neuroanatomy topic identified through a baseline assessment.

Studieoversikt

Detaljert beskrivelse

The study will be conducted in three phases. In Phase 1, students will receive traditional neuroanatomy teaching followed by a 50-item single-best-answer assessment, topic difficulty ratings, and confidence ratings to identify the most challenging neuroanatomy topic.

In Phase 2, students will be randomly allocated after stratification based on previous module academic performance. Group A will receive an integrated multimodal digital and specimen-based neuroanatomy teaching session, while Group B will receive a traditional specimen-based revision session as a wait-list control. Both groups will receive a 90-minute structured teaching session covering identical learning objectives.

In Phase 3, students will complete an immediate post-intervention 20-item single-best-answer assessment and confidence questionnaire. Group B will subsequently receive the integrated multimodal digital and specimen-based teaching intervention.

Studietype

Intervensjonell

Registrering (Antatt)

114

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Shan State
      • Taunggyi, Shan State, Burma, 06017
        • University of Medicine, Taunggyi
        • Ta kontakt med:

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

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Medical Year 2 students enrolled in the Neurology and Mental Health Module.
  • Students who provide informed consent.

Exclusion Criteria:

  • Students absent during intervention sessions.
  • Students who do not complete both pre- and post-tests.

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: Integrated Multimodal Digital and Specimen-Based Teaching

A 90-minute structured integrated multimodal digital and specimen-based neuroanatomy teaching session using virtual dissection, three-dimensional digital visualization, pathway animations/drawing/mapping, sectional CT/MRI imaging, physical 3D models, specimen-based learning, interactive learning activities, and clinical case integration.

Participants assigned to the intervention group will receive integrated multimodal neuroanatomy teaching using multiple complementary learning modalities. The intervention will incorporate 3D virtual dissection and anatomical segmentation using the Asclepius virtual dissection table, physical anatomical specimens and three-dimensional models, pathway animation and instructor-guided drawing/mapping, two-dimensional CT/MRI brain cross-sectional images, and case-based learning (CBL). These modalities will be integrated around the selected difficult neuroanatomy topic to facilitate three-dimensional spatial understanding, anatomical relationships, pathway organization, and clinical application.

The intervention will be delivered by the same instructor using a standardized teaching session. Participants in the wait-list control group will receive the integrated multimodal neuroanatomy teaching after completion of the post-intervention assessment.

Aktiv komparator: Traditional Specimen-Based Revision

A 90-minute structured traditional specimen-based revision session consisting of a brief review lecture and demonstration of formalin-fixed anatomical specimens, following standardized learning objectives and teaching materials.

Participants assigned to the active comparator group will receive traditional specimen-based neuroanatomy revision using formalin-fixed anatomical specimens and instructor-guided review of relevant anatomical structures and relationships. The session will follow the conventional specimen-based teaching approach used for neuroanatomy revision.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Post-intervention knowledge score
Tidsramme: Immediately after the intervention session

Score on the 20-item Single-Best-Answer Assessment of the selected difficult neuroanatomy topic, ranging from 0 to 20, with higher scores indicating better knowledge.

Immediately after the intervention session

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Confidence level
Tidsramme: Immediately after the intervention session

Participants' confidence in learning the selected difficult neuroanatomy topic, assessed using a 5-point Likert scale ranging from 1 to 5, with higher scores indicating greater confidence.

Immediately after the intervention session
Perceived learning difficulty
Tidsramme: Immediately after the intervention session

Participants' perceived difficulty of the selected neuroanatomy topic, assessed using a 5-point Likert scale ranging from 1 to 5, with higher scores indicating greater perceived difficulty.

Immediately after the intervention session

Samarbeidspartnere og etterforskere

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

Sponsor

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)

29. september 2026

Primær fullføring (Antatt)

2. oktober 2026

Studiet fullført (Antatt)

2. oktober 2026

Datoer for studieregistrering

Først innsendt

19. september 2026

Først innsendt som oppfylte QC-kriteriene

19. september 2026

Først lagt ut (Faktiske)

25. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

29. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

24. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 3-IR-ERC-UMTGI-1-2026

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

Individual participant data will not be shared because the study involves individual-level educational data from medical students. Although the data will be de-identified for analysis, access to the participant-level dataset will be restricted to the research team to protect participant privacy and confidentiality.

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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