NCT07086170

Brief Summary

This randomized controlled trial aimed to evaluate the effect of psychological first aid (PFA) training on disaster response and psychological first aid application self-efficacy among nursing students. The study included 132 participants, with 72 in the intervention group and 60 in the control group. The intervention group received six 60-minute online PFA training sessions over three weeks. Data were collected using the Personal Information Form, Disaster Response Self-Efficacy Scale (DRSES), and the Psychological First Aid Application Self-Efficacy Scale. After the training and follow-up, the intervention group showed significantly higher self-efficacy scores across all DRSES sub-dimensions and in applying PFA, compared to the control group. Findings suggest that integrating PFA training into nursing education can enhance students' readiness and competence in disaster response.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
132

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Apr 2023

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

Study Start

First participant enrolled

April 2, 2023

Completed
18 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 20, 2023

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 20, 2023

Completed
2 years until next milestone

First Submitted

Initial submission to the registry

July 18, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 25, 2025

Completed
Last Updated

July 25, 2025

Status Verified

July 1, 2025

Enrollment Period

18 days

First QC Date

July 18, 2025

Last Update Submit

July 18, 2025

Conditions

Keywords

Disasterpsychological first aidnursing studentsrandomized controlled trial

Outcome Measures

Primary Outcomes (2)

  • Disaster Response Self-Efficacy Scale

    Developed by Hong-Yan Li et al. (2017), this scale assesses individuals' perceived self-efficacy in effectively responding to disasters. The Turkish adaptation, including validity and reliability studies, was conducted by Koca et al. (2018). The scale consists of 19 items across three sub-dimensions, rated on a five-point Likert scale ranging from 1 (No self-confidence) to 5 (Full self-confidence). Higher total scores reflect greater self-efficacy in disaster response. The original study reported excellent internal consistency, with a Cronbach's alpha of 0.96 for the overall scale, and 0.93 for each sub-dimension: On-site Rescue Competence, Psychological Nursing Competence in Disaster, and Quality of Role Undertaken in Disaster and Adaptation Competence.21 In the present study, Cronbach's alpha values ranged from 0.87 to 0.93 across groups and time points, confirming the scale's reliability in this sample

    aseline, post-intervention (Week 3), and follow-up (Month 3)

  • Psychological First Aid Application Self-Efficacy Scale

    Developed by Kılıç Bayageldi and Şimşek (2022), this scale assesses self-efficacy in applying Psychological First Aid (PFA). It consists of 35 items within a single sub-dimension, rated on a five-point Likert scale from 1 (Not at all appropriate) to 5 (Completely appropriate). Total scores range from 35 to 175, with no reverse-scored items. Higher scores indicate greater self-efficacy in PFA application. The scale demonstrated excellent reliability, with a Cronbach's alpha of 0.95 and a test-retest correlation coefficient of 0.93.22 In this study, internal consistency remained high across all measurements, with Cronbach's alpha values between 0.89 and 0.96.

    aseline, post-intervention (Week 3), and follow-up (Month 3)

Study Arms (2)

Intervention Group

EXPERIMENTAL

This group received online psychological first aid (PFA) training. Students were randomly divided into four subgroups. Each group received six 60-minute sessions over three weeks. Sessions included slides, videos, Q\&A, role-plays, and case-based discussions. Group members shared thoughts, asked questions, and practiced PFA scenarios. A 17-minute PFA video was also shown. The training was delivered by the researcher and emphasized core PFA principles such as safety, calmness, and self-efficacy.

Other: Psychological First Aid Training

Control Group

NO INTERVENTION

Participants in this group did not receive any training during the study period. They continued with their standard nursing curriculum without any additional intervention.

Interventions

Structured training based on psychological first aid principles. Delivered in six 60-minute sessions over three weeks. Includes theoretical content, interactive methods, and case-based exercises to build disaster response competencies.

Also known as: PFA Training
Intervention Group

Eligibility Criteria

Age21 Years - 24 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Were fourth-year nursing students at the participating universities
  • Had not previously participated in similar training that could bias results
  • Had not received any prior psychological first aid (PFA) training or services
  • Had no internet access problems during the intervention period -

You may not qualify if:

  • Students who withdrew from the study voluntarily during the intervention process
  • Participants who experienced technical issues that prevented their attendance in most training sessions
  • Individuals with prior experience in psychological first aid or formal training in disaster response

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Artvin Coruh University

Artvin, 08000, Turkey (Türkiye)

Location

Study Officials

  • Nurhayat KILIÇ BAYAGELDİ, PhD

    Artvin Coruh University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Open-label design; no blinding was used.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: A randomized controlled trial was conducted according to the CONSORT guideline.
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

July 18, 2025

First Posted

July 25, 2025

Study Start

April 2, 2023

Primary Completion

April 20, 2023

Study Completion

July 20, 2023

Last Updated

July 25, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations