Disaster Nursing Education in Family Health Centers
August 15, 2026 updated by: Ömer Şahin, University of Gaziantep
The Effect of Education Based on the Jennings Disaster Nursing Management Model on Disaster Preparedness Perception, Self-Efficacy, and Resilience: A Randomized Controlled Study in Family Health Centers
This study examines the effect of a training program based on the Jennings Disaster Nursing Management Model on disaster preparedness perception, self-efficacy, and resilience among nurses working in family health centers in Hatay, Turkey.
Participants will be randomly assigned to either an intervention group, which will receive a 14-week structured training program, or a control group, which will not receive the training during the study period.
Preparedness perception, self-efficacy, and resilience will be measured before and after the intervention using standardized questionnaires.
The study aims to determine whether this training improves nurses' readiness to respond to disasters in primary health care settings.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
52
Phase
- Not Applicable
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Registered nurse currently working at a family health center (ASM) in Hatay Province
- Voluntary agreement to participate in the study
- No prior participation in a disaster nursing training program based on the Jennings model
Exclusion Criteria:
- Nurses on extended leave during the study period
- Nurses who do not complete the baseline assessment
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention Group
Nurses in this group will receive a 14-week training program based on the Jennings Disaster Nursing Management Model, delivered in approximately 30-minute in-person sessions.
|
A 14-week structured training program based on the Jennings Disaster Nursing Management Model, delivered through approximately 30-minute face-to-face sessions, designed to improve disaster preparedness perception, self-efficacy, and resilience among family health center nurses.
|
|
No Intervention: Control Group
Nurses in this group will not receive the training program during the study period and will continue routine practice.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Disaster Preparedness Perception Score
Time Frame: Baseline and immediately after completion of the 14-week training program
|
Assessed using the Disaster Preparedness Perception Scale (HAHAÖ), a 20-item scale with three subdimensions (Preparedness, Response, Post-Disaster Period).
Higher scores indicate greater preparedness perception.
|
Baseline and immediately after completion of the 14-week training program
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
August 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Study Registration Dates
First Submitted
August 15, 2026
First Submitted That Met QC Criteria
August 15, 2026
First Posted (Actual)
August 20, 2026
Study Record Updates
Last Update Posted (Actual)
August 20, 2026
Last Update Submitted That Met QC Criteria
August 15, 2026
Last Verified
August 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- GAUN-ASM-AFET-2026
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.