NCT06677398

Brief Summary

In simulation-based training, the debriefing session is considered a cornerstone of learning. Therefore, this study aims to compare two different methods of debriefing sessions.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
109

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2024

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

November 2, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

November 6, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 29, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 29, 2025

Completed
Last Updated

February 11, 2025

Status Verified

February 1, 2025

Enrollment Period

3 months

First QC Date

November 2, 2024

Last Update Submit

February 7, 2025

Conditions

Keywords

DebriefingFeedbackEffectivenessPatient SimulationVirtual SystemsNursing Students

Outcome Measures

Primary Outcomes (3)

  • Hypothesis 1

    There is a difference in the Simulation Effectiveness Tool scores between students using debriefing methods.

    1 week

  • Hypothesis 2

    There is a difference in the Debriefing Experience Scale scores between students using debriefing methods.

    1 week

  • Hypothesis 3

    There is a difference in The Student Satisfaction and Self-confidence scores between students using debriefing methods.

    1 week

Study Arms (3)

Group A

EXPERIMENTAL

Experimental group that used one of the debriefing methods

Other: Debriefing Method 1

Group B

EXPERIMENTAL

Experimental group that used one of the debriefing methods

Other: Debriefing Method 2

Group C

OTHER

A control group that used none of the debriefing methods

Other: Debriefing Method VP

Interventions

The researchers used a debriefing method that they chose after a virtual simulation

Group A

The researchers used the debriefing method that virtual patient simulator presents

Group C

The researchers used a debriefing method that they chose after a virtual simulation

Group B

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Being 4th grade nursing student at a nursing faculty

You may not qualify if:

  • Not having participated in simulation before and not having practiced with a virtual patient.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Health Sciences Turkey, Gulhane Faculty of Nursing

Ankara, Etlik, Turkey (Türkiye)

Location

Related Publications (3)

  • Dreifuerst, K.T., 2015. Getting started with debriefing for meaningful learning. Clin Simul Nurs 11, 268-275. https://doi.org/10.1016/j.ecns.2015.01.005

    BACKGROUND
  • Decker, S., Alinier, G., Crawford, S.B., Gordon, R.M., Jenkins, D., Wilson, C., 2021. Healthcare Simulation Standards of Best PracticeTM The Debriefing Process. Clin Simul Nurs 58, 27-32. https://doi.org/10.1016/j.ecns.2021.08.011

    BACKGROUND
  • Cheng A, Kessler D, Mackinnon R, Chang TP, Nadkarni VM, Hunt EA, Duval-Arnould J, Lin Y, Cook DA, Pusic M, Hui J, Moher D, Egger M, Auerbach M; International Network for Simulation-based Pediatric Innovation, Research, and Education (INSPIRE) Reporting Guidelines Investigators. Reporting guidelines for health care simulation research: extensions to the CONSORT and STROBE statements. Adv Simul (Lond). 2016 Jul 25;1:25. doi: 10.1186/s41077-016-0025-y. eCollection 2016.

    PMID: 29449994BACKGROUND

Related Links

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Parallel group-randomized trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Asst. Prof

Study Record Dates

First Submitted

November 2, 2024

First Posted

November 6, 2024

Study Start

November 1, 2024

Primary Completion

January 29, 2025

Study Completion

January 29, 2025

Last Updated

February 11, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will not share

Researchers believe that it is important to share the data of the study with other researchers following the completion of the data.

Locations