NCT06438029

Brief Summary

Due to the increase in disasters, humanity is facing an increasing threat to life and property. Disasters occur with little warning and can last for hours or months. Existing literature reveals that most nurses are not prepared for a disaster in the community. Continuous preparedness requires the involvement of staff and nursing students in the development, review and implementation of the disaster plan. The development of ongoing, easily accessible, engaging and realistic educational programmes is best for the acquisition of skills and competence. An experimental study with pretest-posttest control group The project is planned to be conducted with the fourth grade students of the Department of Nursing, Faculty of Health Sciences, Fırat University in a randomised controlled study model with pre-test-post-test control group. The population of the study will consist of the fourth year students of the Department of Nursing, Faculty of Health Sciences, Fırat University. The sample will consist of 90 students with 0.05 error, 0.95 confidence interval, 0.95 confidence interval, 0.6 effect size and 0.80 representation power of the universe with the power analysis. These students will be divided into 45 experimental and 45 control groups. In the first stage of the study, the experimental and control group students were asked to complete the "Personal Information Form" and '' Disaster response self-efficacy scale" will be filled. In the second stage of the research, the students in the experimental group will be given a detailed and planned training programme. After the training, the students

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

May 27, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

May 31, 2024

Completed
5 months until next milestone

Study Start

First participant enrolled

October 15, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 15, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 15, 2025

Completed
Last Updated

March 13, 2025

Status Verified

March 1, 2025

Enrollment Period

3 months

First QC Date

May 27, 2024

Last Update Submit

March 11, 2025

Conditions

Keywords

Natural disastersNursing students

Outcome Measures

Primary Outcomes (1)

  • Disaster response self-efficacy scale:

    The scale is a 5-point Likert type and consists of a total of 19 items and 3 sub-dimensions (On-site rescue competence, Disaster psychological nursing competence, Nature of the role undertaken in disaster and adaptation competence). The scale is answered as having no self-confidence (1 point), basically no self-confidence (2 points), some self-confidence (3 points), basically self-confident (4 points) and full self-confidence (5 points). The scale score is calculated by summing the answers to the questions. A high score from the scale indicates high disaster response self-efficacy. In the Turkish validity and reliability study of the scale, the Cronbach alpha coefficient was found to be 0.96.

    3 month

Study Arms (2)

Education group

EXPERIMENTAL

The forms used in the study were collected by the researcher through face-to-face interviews in seminar halls in schools. Firstly, the students in the experimental group will be trained on disaster and disaster response. The trainings were organised as a total of four sessions with a two-week interval of twenty minutes in each session. Personal Information Form and Disaster Intervention Self-Efficacy Scale were filled as pre-test in the seminar halls of the schools under the supervision of the researcher.

Other: Education groupOther: control group

Control group

NO INTERVENTION

Personal Information Form and Disaster Response Self-Efficacy Scale will be applied to the students in the control group as a pre-test. No training will be given to the control group. In the last stage of the research, the Disaster Response Self-Efficacy Scale will be applied to the control group as a post-test and the data collection process will be terminated. After the last test was applied to the groups, training materials will be given to the people who demanded from the control group.

Interventions

the students in the experimental group will be trained on disaster and disaster response

Education group

the students in the experimental group will be trained on disaster and disaster response

Education group

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Being a 4th year Nursing Student
  • Want to participate in the research voluntarily

You may not qualify if:

  • Student wants to leave the study
  • Incomplete filling of survey forms

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Firat University

Elâzığ, 23119, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Control Groups

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Masking Details
Randomisation method will be used to determine how the experimental and control groups will be separated at the beginning of the study (13). As the randomisation method, "simple randomisation method" was chosen in order to provide equal number of samples in two groups. Randomisation will be performed using https://www.randomizer.org/ website in computer environment. According to the randomisation outputs, the individuals to be included in the experimental and control groups will be listed. Columns between 1-90 will be created in the system. Patients will be randomly assigned to the groups by considering the numbers 1 and 2 in the columns (nursing education group 1 and control group 2).
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: This research is a randomised control study with pretest-posttest design.
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
assistant professor

Study Record Dates

First Submitted

May 27, 2024

First Posted

May 31, 2024

Study Start

October 15, 2024

Primary Completion

January 15, 2025

Study Completion

January 15, 2025

Last Updated

March 13, 2025

Record last verified: 2025-03

Locations