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Web-Based End-of-Life and Post-Mortem Care Education for Nursing Students

NCT07737028 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2027-02
Last updated
2026-08-04

Condition(s) studied

End-of-Life and Post-Mortem Care Education

Investigational drug(s) / intervention(s)

Web-Based End-of-Life and Post-Mortem Care EducationFace-to-Face Case Discussion Sessions

Web-Based End-of-Life and Post-Mortem Care Education: Participants assigned to the experimental group will receive a web-based educational program consisting of eight structured online modules covering end-of-life and post-mortem care. The program is delivered through a dedicated web-based learning platform and includes narrated presentations, visual materials, case-based learning activities, and interactive educational resources. The intervention is designed to be completed over a two-month period, with sequential access to the modules to ensure completion of all educational content.

Face-to-Face Case Discussion Sessions: Participants assigned to the control group will participate in three face-to-face case discussion sessions focusing on end-of-life and post-mortem care according to the study protocol. During the intervention period, participants in the control group will not have access to the web-based educational platform. After completion of data collection, access to the web-based educational materials will be provided.

Study summary

This study aims to evaluate the effect of a web-based end-of-life and post-mortem care education program on nursing students' post-mortem self-efficacy, death literacy, and attitudes toward the principles of a dignified death. Participants will receive educational content through an online learning platform, and the effectiveness of the program will be assessed using validated questionnaires administered before and after the intervention. The findings are expected to support the development of accessible, sustainable, and effective digital education programs that enhance nursing students' knowledge, skills, and attitudes related to end-of-life and post-mortem care.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Fourth-year undergraduate nursing students enrolled at the Faculty of Health Sciences, Necmettin Erbakan University, during the 2026-2027 Spring semester. * Successful completion of the Fundamentals of Nursing, Medical Nursing, and Psychiatric and Mental Health Nursing courses. * Access to an internet-enabled device. * Willingness to participate and provide informed consent. Exclusion Criteria: * Failure to complete at least one educational module. * Failure to complete the baseline, post-intervention, or follow-up assessments. * Withdrawal from the study at any time.

Primary outcome measure(s)

  • Post-Mortem Self-Efficacy — Baseline, immediately after completion of the 2-month intervention (approximately 2 months), and 2-month follow-up (approximately 4 months from baseline).
    Change in nursing students' post-mortem self-efficacy will be measured using the End-of-Life and Post-Mortem Self-Efficacy Scale for Nursing Students. Total scores range from 0 to 100, with higher scores indicating greater self-efficacy in end-of-life and post-mortem care.

Trial sites (1)

FacilityCityRegionStatus
Seydişehir Kamil Akkanat Faculty of Health Sciences, Necmettin Erbakan University Konya Seydisehir
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07737028 on ClinicalTrials.gov ↗ ← All trials in Turkey