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

24. september 2026 opdateret af: 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.

Studieoversigt

Detaljeret 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.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

114

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

    • Shan State
      • Taunggyi, Shan State, Burma, 06017
        • University of Medicine, Taunggyi
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Barn
  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

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

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Andet
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
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
Foranstaltningsbeskrivelse
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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

29. september 2026

Primær færdiggørelse (Anslået)

2. oktober 2026

Studieafslutning (Anslået)

2. oktober 2026

Datoer for studieregistrering

Først indsendt

19. september 2026

Først indsendt, der opfyldte QC-kriterier

19. september 2026

Først opslået (Faktiske)

25. september 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

29. september 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

24. september 2026

Sidst verificeret

1. september 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 3-IR-ERC-UMTGI-1-2026

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

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.

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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