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Simulation-Based Disaster Preparedness Education for Nursing Students (SimDisaster)

9. listopadu 2026 aktualizováno: Atılım University

Simulation-Based Disaster Education to Improve Disaster Preparedness Among Nursing Students: A Randomized Controlled Trial

This randomized controlled trial aims to evaluate the effects of web-based interactive learning and simulation-based disaster education on disaster preparedness among senior nursing students. The study will also evaluate the effects of the educational program on students' disaster response self-efficacy, psychological preparedness for disaster threats, disaster management knowledge, and practical skills.

The study will be conducted with senior nursing students from three universities. Students who voluntarily agree to participate and meet the eligibility criteria will be randomly assigned to the intervention or control group following baseline assessments. To achieve balance between the groups, stratified randomization will be performed considering baseline Disaster Management Knowledge Test scores, previous disaster education, previous participation in simulation activities, and previous disaster experience.

Both groups will receive the same disaster education content developed in accordance with the International Council of Nurses (ICN) core competencies in disaster nursing. The educational content consists of three main modules: prevention and preparedness, response, and recovery and rehabilitation.

Students in the intervention group will receive the educational content through a web-based disaster learning and teaching platform. In addition to the educational modules, the platform will include interactive learning activities and scenario-based case analyses to reinforce learning. After completing the web-based educational modules, students will participate in three disaster simulation scenarios at a simulation center. These scenarios will address emergency care, intensive care, and rehabilitation processes related to disaster management.

Students in the control group will receive the same disaster education content through conventional PowerPoint-based instructional materials. Therefore, the main difference between the groups will not be the educational content itself, but the method of delivery and the interactive web-based learning and simulation components provided to the intervention group. After completion of post-intervention data collection, the educational program provided to the intervention group will also be made available to students in the control group.

Students' perceptions of disaster preparedness, disaster response self-efficacy, psychological preparedness for disaster threats, disaster management knowledge, and practical skills will be assessed using pre-intervention and post-intervention measurements. In the intervention group, the web-based learning environment will also be evaluated in terms of usability and students' perceptions of the platform. Simulation performance will be assessed using scenario-specific checklists and skill assessment tools developed for the study.

The study is designed to determine whether integrating web-based interactive learning and simulation-based education into disaster nursing education improves nursing students' preparedness, knowledge, self-efficacy, psychological preparedness, and practical skills compared with conventional delivery of the same educational content.

Přehled studie

Typ studie

Intervenční

Zápis (Odhadovaný)

102

Fáze

  • Nelze použít

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní kontakt

Studijní místa

      • Diyarbakır, Turecko (Türkiye)
        • Adıyaman University
        • Kontakt:
      • Istanbul, Turecko (Türkiye)
        • Acıbadem Mehmet Ali Aydınlar University
        • Kontakt:
    • Ankara
      • Ankara, Ankara, Turecko (Türkiye), 06830

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

18 let a starší (Dospělý, Starší dospělý)

Přijímá zdravé dobrovolníky

Ano

Pohlaví způsobilá ke studiu

Všechno

Popis

Inclusion Criteria:

  • • Be a senior (final-year) nursing student;

    • Own and use a smart device capable of accessing the educational platform;
    • Have access to an internet connection;
    • Be able to understand and communicate in Turkish; and
    • Voluntarily agree to participate in the study.

Exclusion Criteria:

  • Do not complete the educational content provided through the web-based learning and teaching platform;
  • Do not participate in the simulation center scenarios;
  • Request to withdraw from the study at any stage; or
  • Do not complete the study data collection forms, including the pretest and posttest assessments

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Jiný
  • Přidělení: Randomizované
  • Intervenční model: Paralelní přiřazení
  • Maskování: Singl

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Experimentální: Web-Based Disaster Education and Simulation Group

Participants in this arm will receive a web-based disaster education program developed based on disaster nursing competencies, followed by simulation-based training. The web-based program includes interactive learning activities, case scenarios, quizzes, and gamification elements. After completing the web-based education, participants will take part in simulation scenarios addressing disaster-related nursing care.

Participants will receive a web-based disaster education program developed based on disaster nursing competencies, followed by simulation-based training. The web-based program consists of three modules addressing disaster prevention and preparedness, disaster response, and recovery and rehabilitation. It includes interactive learning activities, case scenarios, quizzes, and gamification elements such as points, badges, and a leaderboard. After completing the web-based program, participants will participate in simulation-based training involving disaster-related nursing care scenarios. The intervention is designed to improve nursing students' disaster knowledge, preparedness, response self-efficacy, psychological preparedness, and disaster-related nursing skills.

Aktivní komparátor: Conventional PowerPoint-Based Disaster Education

Participants assigned to the control group will receive disaster nursing education using conventional PowerPoint-based teaching. The educational content will cover the same core disaster nursing topics as the web-based educational program; however, interactive and gamification features will not be included.

Participants assigned to the control group will receive conventional PowerPoint-based disaster nursing education. The educational content will cover the same core disaster nursing topics as the web-based educational program, including disaster prevention and preparedness, disaster response, and recovery and rehabilitation. The content will be delivered using conventional PowerPoint presentations without interactive learning activities, gamification elements, or web-based features.

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Change in Perceived Disaster Preparedness
Časové okno: Intervention group: Before web-based learning and within 2 weeks after completing simulation training. Control group: Before PowerPoint-based education and within 2 weeks after completing PowerPoint-based education.

The Scale of Perception of Disaster Preparedness on Nurses was developed to measure nurses' perceptions of their preparedness for disaster management.The scale consists of 20 items across three subscales: preparedness (items 1-6), response (items 7-15), and post-disaster (items 16-20). Each item is rated on a 5-point Likert scale: 1 = strongly disagree, 2 = disagree, 3 = partially agree, 4 = agree, and 5 = strongly agree. Total scores range from 20 to 100, with higher scores indicating greater perceived disaster preparedness.

Intervention group: Before web-based learning and within 2 weeks after completing simulation training. Control group: Before PowerPoint-based education and within 2 weeks after completing PowerPoint-based education.
Change in Disaster Response Self-Efficacy
Časové okno: Intervention group: Before web-based learning and within 2 weeks after completing simulation training. Control group: Before PowerPoint-based education and within 2 weeks after completing PowerPoint-based education.

Disaster response self-efficacy will be assessed in both groups using the Disaster Response Self-Efficacy Scale. The scale consists of 19 items across three subscales. Each item is rated on a 5-point Likert scale (1 = not at all confident, 2 = generally not confident, 3 = somewhat confident, 4 = generally confident, and 5 = fully confident). The mean item score ranges from 1.00 to 5.00, with higher scores indicating greater disaster response self-efficacy. Mean scores are classified as low (1.00-2.33), moderate (2.34-3.67), or high (3.68-5.00).

Intervention group: Before web-based learning and within 2 weeks after completing simulation training. Control group: Before PowerPoint-based education and within 2 weeks after completing PowerPoint-based education.
Change in Psychological Preparedness for Disaster Threat
Časové okno: Intervention group: Before web-based learning and within 2 weeks after completing simulation training. Control group: Before PowerPoint-based education and within 2 weeks after completing PowerPoint-based education.

Psychological preparedness for disaster threats will be assessed in both groups using the 21-item Turkish version of the Psychological Preparedness for Disaster Threat Scale (PPDTS-T21). Each item is scored from 1 to 4. The scale has three subscales. Knowledge and Management of the External Situational Environment (9 items) and Management of One's Emotional and Psychological Response (9 items) each range from 9 to 36. Management of One's Social Environment (3 items) ranges from 3 to 12. The three subscale scores are summed to obtain a total score ranging from 21 to 84. Higher scores indicate greater psychological preparedness for disaster threats.

Intervention group: Before web-based learning and within 2 weeks after completing simulation training. Control group: Before PowerPoint-based education and within 2 weeks after completing PowerPoint-based education.
Change in Disaster Management Knowledge
Časové okno: Baseline: Before randomization and blinding in both groups. Posttest: Within 2 weeks after completing simulation training (intervention group) or PowerPoint-based education (control group).

Disaster management knowledge will be assessed using the Disaster Management Knowledge Test. The research team will develop the test based on the educational content after that content has been finalized with input from experts. Higher scores indicate greater knowledge of disaster management.

Baseline: Before randomization and blinding in both groups. Posttest: Within 2 weeks after completing simulation training (intervention group) or PowerPoint-based education (control group).
Disaster-Related Nursing Skill Performance
Časové okno: Posttest only: Within 2 weeks after completing simulation training in the intervention group and within 2 weeks after completing PowerPoint-based education in the control group.

Disaster-related nursing skills will be assessed at posttest in both groups using skill checklists in the basic skills laboratories of the participating universities. The checklists are based on the Turkish Ministry of Health's Basic First Aid Skills Guide. The Triage Skills Checklist assesses patient prioritization and assignment to the red, yellow, green, and black triage categories. The Basic Life Support and First Aid Skills Checklist assesses performance on a manikin in a simulated emergency. An observer rates 16 procedural steps from 0 to 4 (0 = not assessed, 1 = needs improvement, 2 = fair, 3 = good, 4 = competent). If all 16 step ratings are summed, the total score ranges from 0 to 64. Higher scores indicate better performance.

Posttest only: Within 2 weeks after completing simulation training in the intervention group and within 2 weeks after completing PowerPoint-based education in the control group.

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Evaluation of the Web-Based Learning Environment
Časové okno: Within 2 weeks after completion of the web-based education program (intervention group only).

Participants in the intervention group will evaluate the web-based learning environment using the Turkish version of the Web-Based Learning Environment Evaluation Scale. The scale comprises 40 items across four subscales (teaching strategy, teaching material, learning tools, and learning interface). Each item is rated on a 5-point Likert scale ranging from 1 (not at all important) to 5 (very important). Total scores range from 40 to 200, with higher scores indicating that participants assign greater importance to the features of the web-based learning environment.

Within 2 weeks after completion of the web-based education program (intervention group only).

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Odhadovaný)

1. února 2027

Primární dokončení (Odhadovaný)

1. dubna 2027

Dokončení studie (Odhadovaný)

1. dubna 2027

Termíny zápisu do studia

První předloženo

25. srpna 2026

První předloženo, které splnilo kritéria kontroly kvality

9. listopadu 2026

První zveřejněno (Aktuální)

12. listopadu 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

12. listopadu 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

9. listopadu 2026

Naposledy ověřeno

1. srpna 2026

Více informací

Termíny související s touto studií

Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

NE

Popis plánu IPD

Individual participant data (IPD) will not be shared because data sharing with external researchers is not included in the current study protocol or informed consent process.

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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