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

9 novembre 2026 aggiornato da: 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.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

102

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

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

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

Sì

Sessi ammissibili allo studio

Tutto

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.

Comparatore attivo: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Perceived Disaster Preparedness
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Evaluation of the Web-Based Learning Environment
Lasso di tempo: 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).

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 febbraio 2027

Completamento primario (Stimato)

1 aprile 2027

Completamento dello studio (Stimato)

1 aprile 2027

Date di iscrizione allo studio

Primo inviato

25 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

9 novembre 2026

Primo Inserito (Effettivo)

12 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

12 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

9 novembre 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano 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.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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