Role Model-Based Ethics Education and Moral Injury Prevention in Second-Year Medical Students
1 other identifier
interventional
101
1 country
1
Brief Summary
This study examines whether role model-based ethics education can reduce moral injury and perceived stress, and improve resilience, among second-year medical students in Taiwan. Students participated in a general education ethics course and self-selected into one of two groups: a standard-intensity group receiving role model narratives and guided handouts, or an enhanced-intensity group receiving the same content plus reflective writing assignments and live guest appearances by featured practitioners. Validated questionnaires measuring moral injury (MIDS), perceived stress (PSS-14), and resilience (CD-RISC-10) were administered before and after the course. Open-ended written responses were also collected and analyzed. The study aims to inform early curricular integration of ethics education in medical training and to identify instructional designs that support moral agency without inadvertently promoting emotional disengagement.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 20, 2026
CompletedFirst Submitted
Initial submission to the registry
June 11, 2026
CompletedFirst Posted
Study publicly available on registry
June 18, 2026
CompletedJune 18, 2026
June 1, 2026
2 months
June 11, 2026
June 14, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Moral Injury (MIDS)
Moral injury symptoms measured using the Moral Injury and Distress Scale (MIDS). Higher scores indicate greater moral injury.
Baseline and up to 6 weeks (immediately after course completion)
Secondary Outcomes (1)
Perceived Stress (PSS-14)
Baseline and up to 6 weeks (immediately after course completion)
Other Outcomes (1)
Resilience (CD-RISC-10)
Baseline and up to 6 weeks (immediately after course completion)
Study Arms (2)
Standard-Intensity Group (Group A)
ACTIVE COMPARATORParticipants received role model narratives and guided reflection handouts as part of a semester-long general education ethics course.
Enhanced-Intensity Group (Group B)
EXPERIMENTALParticipants received the same role model narratives and guided reflection handouts as Group A, supplemented with structured reflective writing assignments and live guest appearances by the featured practitioners.
Interventions
Participants attended a semester-long general education ethics course incorporating role model narratives drawn from real clinical practitioners. Guided reflection handouts were provided to facilitate structured engagement with the ethical themes presented. This condition served as the active comparator.
Participants attended the same role model-based ethics course as the standard-intensity group, with two additional components: structured reflective writing assignments requiring personal ethical reflection, and live guest appearances by the practitioners featured in the role model narratives. This condition served as the experimental arm.
Eligibility Criteria
You may qualify if:
- Second-year medical students enrolled in a general education ethics course at National Defense Medical University, Taiwan
- Willing to complete pre- and post-course questionnaires
You may not qualify if:
- \- Students who did not complete both pre-test and post-test assessments
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Chun Lun Hsulead
Study Sites (1)
National Defense Medical University
Taipei, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Chun Lun Hsu
National Defense Medical University, Taiwan
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
June 11, 2026
First Posted
June 18, 2026
Study Start
November 1, 2025
Primary Completion
December 31, 2025
Study Completion
February 20, 2026
Last Updated
June 18, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share