# Implementation of a Novel Wilderness Medicine Simulation Course for Medical Students

**Authors:** Katherine A. Sprengel, Sophia Redpath, Kira L. Palazzo, Sara M. Hock

PMC · DOI: 10.15766/mep_2374-8265.11526 · MedEdPORTAL : the Journal of Teaching and Learning Resources · 2025-06-09

## TL;DR

A new wilderness medicine simulation course for medical students boosts confidence and interest in the field.

## Contribution

A novel wilderness medicine simulation curriculum for undergraduate medical students is introduced and evaluated.

## Key findings

- 10 out of 12 students reported increased confidence in managing urgent medical cases after the simulation.
- All students agreed simulation was an effective learning method for wilderness medicine.
- The simulation model is feasible and adaptable for other institutions.

## Abstract

Wilderness medicine is a growing field focused on delivering quality medical care in austere environments. Simulation-based education has proven effective in emergency and wilderness medicine, particularly in graduate medical education. We propose that introducing wilderness medicine concepts earlier in medical education as part of a high-fidelity simulation for medical students could both increase interest in wilderness medicine and have widely applicable educational benefits.

We developed a novel 1-day case-based simulation curriculum to be performed in a wilderness environment and invited undergraduate medical students to participate. A 25-question survey was administered before and after the simulation to assess subjective change across various topics.

The 10 of 12 students who responded to the survey indicated that the simulation significantly increased their confidence in managing urgent medical cases and increased their interest in the wilderness medicine field. All students agreed that simulation was an effective way to learn this material.

Implementing a wilderness medicine simulation in medical curricula appears feasible and provides a comprehensive model that can be easily adapted to other institutions.

## Full-text entities

- **Genes:** AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}
- **Diseases:** allergy (MESH:D004342), Anaphylaxis (MESH:D000707), Hypothermia (MESH:D007035), ecchymosis (MESH:D004438), anxiety (MESH:D001007), fatigue (MESH:D005221), arterial bleed (MESH:D006470), laceration (MESH:D022125), Trimalleolar fracture (MESH:D064386), fracture (MESH:D050723), SAM (MESH:D020914), concussion (MESH:D001924), injuries (MESH:D014947), deformity (MESH:D009140)
- **Chemicals:** epinephrine (MESH:D004837), aluminum (MESH:D000535), diphenhydramine (MESH:D004155), water (MESH:D014867), SAM (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12146433/full.md

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Source: https://tomesphere.com/paper/PMC12146433