NCT06689475

Brief Summary

This randomized controlled study aims to determine the effect of simulation on the cardiac auscultation competence of nursing students. The main questions it aims to answer are:

  • Simulation is effective in developing the cardiac auscultation competence of nursing students.
  • The psychoacoustic approach is effective in developing the cardiac auscultation competence of nursing students. One week after the 2-hour theoretical lecture, all three groups will be taken simultaneously to a 3-hour laboratory practice for cardiac auscultation. An instructor will lead each group to ensure coordination. The psychoacoustic approach group will listen to normal heart sounds (S1, S2), abnormal heart sounds (S3, S4) and murmur sounds from the audio file uploaded to their mobile phones in the laboratory environment through headphones for 500 repetitions each. The simulation group will practice auscultation of heart sounds in a one-to-one and repetitive manner, working with a high reality simulator. Trainers will act as facilitators during the cardiac auscultation practice of the students in the intervention groups. The control group will continue with the standard education.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
57

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2024

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

First Submitted

Initial submission to the registry

November 13, 2024

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 14, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

December 25, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 5, 2025

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 20, 2025

Completed
Last Updated

June 4, 2025

Status Verified

May 1, 2025

Enrollment Period

4 months

First QC Date

November 13, 2024

Last Update Submit

May 30, 2025

Conditions

Keywords

auscultation of cardiac soundsSimulationpsychoacousticnursing students

Outcome Measures

Primary Outcomes (1)

  • achievement test

    It is a four-question test in which students mark the cardiac sounds they listen to on the computer.

    From enrollment to the end of education at 4 weeks.

Secondary Outcomes (1)

  • Student Satisfaction and Confidence in Learning

    At the end of education at 4 weeks.

Study Arms (3)

Psychoacoustic group

EXPERIMENTAL

The psychoacoustic approach group will listen to normal heart sounds (S1, S2), abnormal heart sounds (S3, S4) and murmur sounds from the audio file uploaded to their mobile phones in the laboratory environment through headphones for 500 repetitions each.

Other: Psychoacoustic approach

Simulation group

EXPERIMENTAL

The simulation group will practice auscultation of heart sounds in a one-to-one and repetitive manner, working with a high reality simulator. Trainers will act as facilitators during the cardiac auscultation practice of the students in the intervention groups.

Other: Simulation

Control group

NO INTERVENTION

The control group will continue with the standard education.

Interventions

The psychoacoustic approach group will listen to normal heart sounds (S1, S2), abnormal heart sounds (S3, S4) and murmur sounds from the audio file uploaded to their mobile phones in the laboratory environment through headphones for 500 repetitions each.

Psychoacoustic group

The simulation group will practice auscultation of heart sounds in a one-to-one and repetitive manner, working with a high reality simulator. Trainers will act as facilitators during the cardiac auscultation practice of the students in the intervention groups.

Simulation group

Eligibility Criteria

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

You may qualify if:

  • \- First-time registration in the course.

You may not qualify if:

  • Non-native speakers of the country's native language.
  • Previous graduation from any health-related university.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gazi University Faculty of Nursing

Ankara, Yenimahalle, 06500, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
FACTORIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD

Study Record Dates

First Submitted

November 13, 2024

First Posted

November 14, 2024

Study Start

December 25, 2024

Primary Completion

May 5, 2025

Study Completion

May 20, 2025

Last Updated

June 4, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations