ClinicalTrials.gg
Not yet recruitingNCT07775170Updated Aug 20, 2026

Disaster Nursing Education in Family Health Centers

An interventional study of Jennings Disaster Nursing Management Model-Based Training Program in Disaster Preparedness, sponsored by University of Gaziantep. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-20.

Sponsored by University of Gaziantep · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Disaster Preparedness
03

In context

Lead sponsor

University of Gaziantep is the lead sponsor of 105 studies on the registry; 28 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Nurses on extended leave during the study period
  • Nurses who do not complete the baseline assessment
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
52 participants (estimated)

Study arms

  • 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.

    Behavioral: Jennings Disaster Nursing Management Model-Based Training Program

  • No intervention
    Control Group

    Nurses in this group will not receive the training program during the study period and will continue routine practice.

Interventions

  • BehavioralJennings Disaster Nursing Management Model-Based Training Program

    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.

06

What researchers measure

Primary outcomes

  1. Change in Disaster Preparedness Perception Score

    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.

    Time frame: Baseline and immediately after completion of the 14-week training program

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Aug 2026; primary completion for Dec 2026, 4 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 15, 2026
First posted
Aug 20, 2026
StartEst.
Aug 2026
Primary completionEst.
Dec 2026
CompletionEst.
Dec 2026
Last update
Aug 20, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07775170
Responsible party
Ömer Şahin (Doctoral Student, University of Gaziantep) — Principal investigator
First posted
Aug 20, 2026
Start date
Aug 2026 (estimated)
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Aug 20, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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