The Effect of a Mixed Intervention Structured According to the Integrated Disaster Management System

February 10, 2026 updated by: Kübra Sultan Dengiz, Necmettin Erbakan University

The Effect of a Mixed Intervention Structured According to the Integrated Disaster Management System on Disaster Risk Perception, Disaster Attitude and Brief Resilience Among University Students

Integrated disaster management is defined as a management process that considers all hazards to create a resilient and resilient society capable of coping with disasters, and utilizes all the resources and resources of society to implement the necessary actions and measures in the prevention, mitigation, preparedness, response, and recovery phases of disaster management. Educational interventions for disaster management are the most important initiatives in both risk reduction and crisis management. In this context, the aim of this study is to evaluate the impact of a hybrid intervention structured according to the integrated disaster management system on disaster risk perception, disaster attitudes, and psychological resilience in university students. The students participating in this study will be administered a mixed intervention structured according to the integrated disaster management system (15-week disaster culture course presentation, case studies, simulation, expert conferences, and material development). Because randomization is not possible, the study adopts a quasi-experimental design. However, measures will be taken to reduce the risk of bias by creating a control group, increasing the number of measurements, using a different scale for test measurements, and ensuring that the individuals implementing the interventions, performing data analysis, and performing the measurements are different. The disaster risk perception scale, disaster attitude scale, and brief psychological resilience scale will be used to collect data. Data analysis will be evaluated at a 95% confidence interval and a significance level of p<0.05.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

140

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey (Türkiye)
    • Konya
      • Konya, Konya, Turkey (Türkiye), 42130
        • Necmettin Erbakan University, Faculthy of Nursing

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Registered as a student at the university where the research will be conducted
  • Active participation in the disaster culture course

Exclusion Criteria:

  • There are no exclusion criteria.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: intervention group
Disaster culture course presentations, conferences by Red Crescent personnel and AKUT volunteers, and the integrated disaster management system were structured according to the; Case studies, disaster simulation application, and student material development will be included.
Behavioral: Mixed Intervention
This study is distinguished by the fact that the intervention was conducted on university students, the intervention was structured according to the integrated disaster management system, case studies and simulation were included in the training content, conferences by field professionals in disaster management were included in the initiative, and the study team consisted of doctoral-level researchers.
No Intervention: Control group
no intervention will be implemented.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
disaster risk perception
Time Frame: From enrollment to the end of treatment at 15 weeks
Changes disaster risk perception scores after a structured mixed intervention based on an integrated disaster management system implemented on university students
From enrollment to the end of treatment at 15 weeks
disaster attitude
Time Frame: From enrollment to the end of treatment at 15 weeks
Changes disaster attitude scores after a structured mixed intervention based on an integrated disaster management system implemented on university students
From enrollment to the end of treatment at 15 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
psychological resilience
Time Frame: From enrollment to the end of treatment at 15 weeks
Changes psychological resilience scores after a structured mixed intervention based on an integrated disaster management system implemented on university students
From enrollment to the end of treatment at 15 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Necmettin Erbakan University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 31, 2025

Primary Completion (Actual)

December 25, 2025

Study Completion (Actual)

February 10, 2026

Study Registration Dates

First Submitted

September 30, 2025

First Submitted That Met QC Criteria

December 11, 2025

First Posted (Actual)

December 24, 2025

Study Record Updates

Last Update Posted (Actual)

February 11, 2026

Last Update Submitted That Met QC Criteria

February 10, 2026

Last Verified

December 1, 2025

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 2025/1159

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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