NCT07366125

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2025

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

October 1, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 17, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 26, 2026

Completed
Last Updated

February 6, 2026

Status Verified

February 1, 2026

Enrollment Period

2 months

First QC Date

January 17, 2026

Last Update Submit

February 4, 2026

Conditions

Keywords

Nursingscenariosimulationstudentbasic life supportpractical skillsself-efficacy

Outcome Measures

Primary Outcomes (1)

  • Basic Life Support Practice Skills

    Basic life support practice skills were assessed using a standardized skills performance checklist.

    Baseline (pre-test), immediately after the intervention (post-test), and 1-month follow-up

Study Arms (2)

Arm 1: Scenario-Based Simulation Group

EXPERIMENTAL

Participants in this group received scenario-based simulation training on basic life support.

Other: Scenario-Based Simulation Training

Arm 2: Standard Training Group

ACTIVE COMPARATOR

Participants in this group received standard theoretical and practical training on basic life support according to the nursing curriculum.

Other: Standard Basic Life Support Training

Interventions

Scenario-based simulation training was provided to improve basic life support skills and self-efficacy among nursing students.

Also known as: Simülasyon Tabanlı Temel Yaşam Desteği Eğitimi
Arm 1: Scenario-Based Simulation Group

Hemşirelik müfredatına uygun olarak verilen standart teorik ve pratik temel yaşam desteği eğitimi.

Arm 2: Standard Training Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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).

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bartin University Faculty of Health Sciences

Bartın, 74100, Turkey (Türkiye)

Location

Study Officials

  • EKER

    Bartin University Faculty of Health Sciences

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
No blinding was applied in this study; both participants and researchers were aware of the group assignments
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Participants were randomly assigned to either the intervention group or the control group. The intervention group received scenario-based simulation training, while the control group received standard basic life support training. Both groups were followed in parallel throughout the study period.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Registered Nurse, MSc Student

Study Record Dates

First Submitted

January 17, 2026

First Posted

January 26, 2026

Study Start

October 1, 2025

Primary Completion

December 1, 2025

Study Completion

December 1, 2025

Last Updated

February 6, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared.

Locations