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Not yet recruitingNCT07770503Updated Aug 18, 2026

PRECEDE-PROCEED BASED FIRST AID TRAINING: SELF-EFFICACY, SKILL AND COST ANALYSIS IN HIGH SCHOLL STUDENTS

An interventional study of First aid training program developed based on the PRECEDE-PROCEED model. and control group in First Aid Training, Adolescent and School Health, sponsored by Izmir Katip Celebi University. Not yet recruiting. Open to participants aged 15 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-18.

Sponsored by Izmir Katip Celebi University · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
187
Allocation
Randomized
Ages
15 Years to 18 Years
Sex
All
01

Study summary

This research has two objectives. Firstly, to determine the effect of a first aid training program, developed based on the PRECEDE-PROCEED model, on the first aid knowledge, self-efficacy, and skill levels of high school students. Secondly, to conduct a cost analysis of the first aid training program. This study is a randomized controlled experimental follow-up study. The research is planned to be conducted in the Aliağa district of İzmir during the fall and spring semesters of the 2026-2027 academic year. The study population will consist of all 10th-grade students who will be studying at the selected high school during the fall semester of the 2026-2027 academic year. Ninth-grade students were excluded from the sample due to their school orientation process, and 11th and 12th-grade students were excluded due to academic intensity and exam anxiety related to their preparation for higher education entrance exams. A complete enumeration method was adopted for sample selection, and all 6 classes (n=187) were included in the study. The sample size calculation was performed based on the information that there are a total of 187 students in 6 different classes currently in 9th grade who will be entering 10th grade in the fall semester of the 2025-2026 academic year.Cluster Randomization was used to assign classes to experimental and control groups. A ranking system was created among the classes using the random.org digital random assignment tool. As a result of this assignment, classes 10-E, 10-D, and 10-F, which ranked first and third respectively, were designated as the Experimental Group, while classes 10-A, 10-C, and 10-B, which ranked third, were designated as the Control Group.To protect student identities and match pre-test and post-test data, a coding system will be used: [Group Letter (D/K)] + [Class/Branch Code] + [Student Sequence/List Number] (e.g., D10B12: The 12th student in the experimental group, class 10-B). To prevent intergroup interaction, the application is designed to be sequential. The experimental group will be applied after all training and data collection processes for the control group are completed. Experimental Group: Before the training, students in the experimental group will be administered a "Personal Information Form, First Aid Information Form, and First Aid Self-Efficacy Scale." Following this, a first aid training program developed based on PRECEDE-PROCEED will be implemented in the students' classrooms. As part of the training program, students will be individually given first aid interventions to assess their skills. Following the training, and then one month and three months after the training, the "First Aid Knowledge Form, First Aid Self-Efficacy Scale, and First Aid Application Skills Assessment Form" will be administered, respectively. Control Group: Students in the control group will be administered the "Personal Information Form, First Aid Knowledge Form, and First Aid Self-Efficacy Scale" before the training. Students will be given brochures based on traditional training methods. For application skills, video training will be conducted on the interactive whiteboard in the control group classrooms. If interactive whiteboards are not available, video training will be conducted for all students in the control group using a projector in the conference halls. After the video presentation, students will be given individual skill practice exercises. Following the brochure and video training, and then one month and three months after the training, the "First Aid Knowledge Form, First Aid Self-Efficacy Scale, and First Aid Application Skills Assessment Form" will be administered, respectively.

02

Conditions studied

  • First Aid Training
  • Adolescent
  • School Health
03

Who can participate

Ages eligible
15 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Participation Criteria:

  • Students enrolled in the relevant high school
  • Students who have received informed consent from their parents or legal guardians.

Exclusion Criteria:

  • Students who have previously received certified first aid training from a professional institution
  • Students with chronic orthopedic, neurological, or cardiovascular conditions that would prevent them from practicing
  • Students who have recently experienced a traumatic accident or loss
  • Students who have left/transferred from the school during the academic term.
04

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
187 participants (estimated)

Study arms

  • Experimental
    Experiment

    The experimental group will receive model-based training.

    Other: First aid training program developed based on the PRECEDE-PROCEED model.

  • Experimental
    Control

    The control group will be given a brochure and shown the video.

    Other: control group

Interventions

  • OtherFirst aid training program developed based on the PRECEDE-PROCEED model.

    The experimental group will receive first aid training based on the PRECEDE-PROCEED model.

  • Othercontrol group

    A video will be shown and brochures will be distributed.

05

What researchers measure

Primary outcomes

  1. First Aid Knowledge Score

    Assessed using the First Aid Knowledge Form developed by the researchers based on current guidelines. The form consists of 26 multiple-choice questions evaluating knowledge across key topics (General Safety, Musculoskeletal Injuries, Bleeding, Choking, Airway Obstruction, and Basic Life Support). Each correct answer is awarded 1 point, with total scores ranging from 0 to 26. Higher scores indicate greater first aid knowledge.

    Time frame: Baseline, 1 month, and 3 months post-training

  2. First Aid Self-Efficacy Score

    Assessed using the First Aid Self-Efficacy Scale (developed by Gülmez Dağ and Çapa Aydın, 2015). The scale contains 25 items rated on a 9-point Likert scale ranging from 1 ("inadequate") to 9 ("very adequate"). The overall score ranges from 25 to 225, calculated by summing all items (subscales include "Life Support First Aid Self-Efficacy" and "Basic First Aid Self-Efficacy"). Higher scores indicate a higher level of perceived self-efficacy in first aid.

    Time frame: Baseline, 1 month, and 3 months post-training

  3. First Aid Practical Skills Score

    Assessed using the First Aid Practical Skills Evaluation Form developed by the researchers. Participants' skill performance is evaluated simultaneously and independently by two blinded first aid instructors. Each step is scored on a 3-point scale: 0 = Not Performed/Incorrect, 1 = Partially/Incompletely Performed, and 2 = Fully and Correctly Performed. Total scores are calculated by summing the steps evaluated, where higher scores reflect better practical skill competence.

    Time frame: Baseline, 1 month, and 3 months post-training

06

Study locations

No study locations are listed for this record.

07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07770503
Lead sponsor
Izmir Katip Celebi University
Responsible party
Medine Yilmaz (Professor Doctor, Izmir Katip Celebi University) — Principal investigator
First posted
Aug 18, 2026
Start date
Oct 5, 2026 (estimated)
Primary completion
Apr 1, 2027 (estimated)
Completion
Dec 1, 2027 (estimated)
Last update
Aug 18, 2026

Study contacts

Medine YILMAZ, Professor Doctor
study director · Izmir Katip Celebi University
Kübra KABALCI, Expert
principal investigator · Izmir Katip Celebi University

Oversight

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

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