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PRECEDE-PROCEED BASED FIRST AID TRAINING: SELF-EFFICACY, SKILL AND COST ANALYSIS IN HIGH SCHOLL STUDENTS
13 augustus 2026 bijgewerkt door: Medine Yilmaz, Izmir Katip Celebi University
THE EFFECT OF A FIRST AID TRAINING PROGRAM DEVELOPED BASED ON THE PRECEDE-PROCEED MODEL ON THE SELF-EFFICACY AND SKILL LEVELS OF HIGH SCHOOL STUDENTS, AND A COST ANALYSIS OF THE PROGRAM.
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.
Studie Overzicht
Toestand
Nog niet aan het werven
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
187
Fase
- Niet toepasbaar
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
- Volwassen
Accepteert gezonde vrijwilligers
Ja
Beschrijving
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.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Fundamentele wetenschap
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Experiment
The experimental group will receive model-based training.
|
The experimental group will receive first aid training based on the PRECEDE-PROCEED model.
|
|
Experimenteel: Control
The control group will be given a brochure and shown the video.
|
A video will be shown and brochures will be distributed.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
First Aid Knowledge Score
Tijdsspanne: Baseline, 1 month, and 3 months post-training
|
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.
|
Baseline, 1 month, and 3 months post-training
|
|
First Aid Self-Efficacy Score
Tijdsspanne: Baseline, 1 month, and 3 months post-training
|
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.
|
Baseline, 1 month, and 3 months post-training
|
|
First Aid Practical Skills Score
Tijdsspanne: Baseline, 1 month, and 3 months post-training
|
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.
|
Baseline, 1 month, and 3 months post-training
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Onderzoekers
- Studie directeur: Medine YILMAZ, Professor Doctor, Izmir Katip Celebi University
- Hoofdonderzoeker: Kübra KABALCI, Expert, Izmir Katip Celebi University
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Geschat)
5 oktober 2026
Primaire voltooiing (Geschat)
1 april 2027
Studie voltooiing (Geschat)
1 december 2027
Studieregistratiedata
Eerst ingediend
8 augustus 2026
Eerst ingediend dat voldeed aan de QC-criteria
13 augustus 2026
Eerst geplaatst (Werkelijk)
18 augustus 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
18 augustus 2026
Laatste update ingediend die voldeed aan QC-criteria
13 augustus 2026
Laatst geverifieerd
1 augustus 2026
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 16.7.2026/0596
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