- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07366125
EFFECT OF SCENARIO-BASED SIMULATION ON BASIC LIFE SUPPORT SKILLS AND SELF-EFFICACY IN NURSING STUDENTS (SBS-BLS)
THE EFFECT OF SCENARİO-BASED SİMULATİON METHOD ON NURSİNG STUDENTS' BASİC LİFE SUPPORT PRACTİCE SKİLLS AND SELF-EFFİCACY LEVELS: A CONTROLLED EXPERİMENTAL STUDY
This study aimed to evaluate the effectiveness of scenario-based simulation in improving nursing students' adult basic life support (ABLS) skills and self-efficacy. Ethical approval was obtained from the Bartın University Social and Human Sciences Ethics Committee, and institutional permission was granted. The study was conducted with students from the Department of Nursing at the Faculty of Health Sciences, Bartın University, between October and December 2025.
The sample size was determined based on the literature using an alpha level of 0.05, an effect size of 0.63, and a statistical power of 85%. A total of 50 students who met the inclusion criteria were randomly assigned to either the experimental or control group. All participants were informed about the study and provided written informed consent.
Data were collected using the Student Information Form, the Adult Basic Life Support Knowledge Level Assessment, the Adult Basic Life Support Skill Performance Assessment Form, and the Student Self-Efficacy Scale. All students received a 90-minute theoretical ABLS training delivered by an experienced researcher. Following the theoretical session, the control group practiced ABLS using the demonstration method on a feedback-enabled manikin, while the experimental group practiced using scenario-based simulation. Both applications were conducted under academic supervision.
Students' knowledge, skill performance, and self-efficacy levels were assessed immediately after training, after the first application, and at a one-month follow-up. Data were analyzed using SPSS version 29.0. No significant difference was found between the groups in knowledge scores immediately after training. After the first application, no significant differences were observed in knowledge or self-efficacy levels; however, skill performance scores were significantly higher in the control group. At the one-month follow-up, a significant decline in skill performance was observed in the control group, whereas the experimental group maintained their performance levels.
These findings indicate that scenario-based simulation supports the long-term retention of practical ABLS skills. Therefore, integrating simulation-based methods into adult basic life support education in nursing programs is recommended.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Bartın, Turkey (Türkiye), 74100
- Bartin University Faculty of Health Sciences
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Voluntarily agreeing to participate in all stages of the research (pre-test - training - post-test, etc.),
- Actively enrolled in a Nursing Undergraduate Program,
- Able to read and understand Turkish,
- Not having any physical or cognitive disability that would prevent participation in practical training,
- Not having received any prior training in TYD (Basic Nursing Education).
Exclusion Criteria:
- Having received any non-research-related training on TYD that you can conduct research on previously,
- Being a graduate of a Health Vocational High School or a graduate of any associate's or bachelor's degree program in the health field,
- Not having registered for courses in the relevant period or having suspended the semester,
- Not regularly attending training sessions during the research process,
- Having serious health problems that will increase the data collection period,
- Incomplete completion of pre-test or post-test forms.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Arm 1: Scenario-Based Simulation Group
Participants in this group received scenario-based simulation training on basic life support.
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Scenario-based simulation training was provided to improve basic life support skills and self-efficacy among nursing students.
Other Names:
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Active Comparator: Arm 2: Standard Training Group
Participants in this group received standard theoretical and practical training on basic life support according to the nursing curriculum.
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Hemşirelik müfredatına uygun olarak verilen standart teorik ve pratik temel yaşam desteği eğitimi.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Basic Life Support Practice Skills
Time Frame: Baseline (pre-test), immediately after the intervention (post-test), and 1-month follow-up
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Basic life support practice skills were assessed using a standardized skills performance checklist.
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Baseline (pre-test), immediately after the intervention (post-test), and 1-month follow-up
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: EKER, Bartin University Faculty of Health Sciences
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- BARUN-MSC-TYD-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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