NCT05672446

Brief Summary

Background: Performing simulation applications using standardized patients provides realistic educational results that support critical thinking and learning, conducted using complex, effective communication scenarios. Objective: This study was planned to evaluate the effect of the use of standardized pediatric patient practice in pediatric nursing education on the ability of nursing students to prepare the child for the procedure. Method: The research was conducted using a convergent parallel design, which is a mixed method design. Ethics committee approval was obtained with the decision numbered 19/376 regarding the ethical suitability of the research. The sample of the study consists of 106 students. The students included in the study were given an introductory information form and the state trait anxiety scale and self-efficacy efficacy scale as pre-tests, and then the theoretical course "Preparing the child for the process according to age periods and communicating with the child patient" was explained. The students were divided into intervention and control groups by randomization. The students in the intervention group participated in the simulation application using standardized pediatric patients. Qualitative data were collected during the debriefing phase of the simulation and student satisfaction and self-confidence in learning scale was applied to the students in the intervention group. Before clinical practice, state trait anxiety scale, self-efficacy scale and perceived learning scale were applied as posttests. During the clinical practice, all students were evaluated in terms of their ability to prepare a real school-age child patient for the procedure.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
106

participants targeted

Target at P50-P75 for not_applicable anxiety

Timeline
Completed

Started Nov 2019

Shorter than P25 for not_applicable anxiety

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

November 5, 2019

Completed
20 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 25, 2019

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2019

Completed
3 years until next milestone

First Submitted

Initial submission to the registry

December 19, 2022

Completed
17 days until next milestone

First Posted

Study publicly available on registry

January 5, 2023

Completed
Last Updated

January 5, 2023

Status Verified

January 1, 2023

Enrollment Period

20 days

First QC Date

December 19, 2022

Last Update Submit

January 4, 2023

Conditions

Keywords

experiental learninganxietypediatric nursingpatient simulationself efficiacyhigh fidelity simulation training

Outcome Measures

Primary Outcomes (1)

  • checklist for preparing the school-age child for processing skill

    The skill checklist for preparing the school-age child for processing was created by the responsible researchers by reviewing the literature (Ball et al., 2014; Conk, Başbakkal, Yılmaz, \& Bolışık, 2013; Çavuşoğlu, 2013). For the content validity of the skill checklist, expert opinion was obtained from the faculty members of Health Sciences University, Gülhane Nursing Faculty, Department of Child Health and Diseases Nursing. The skill checklist for preparing the school-age child for processing consists of 9 items. While evaluating the students, each applied item was marked and it was accepted that the student got a "1" point from that item. Accordingly, a student can get a minimum of "0" and a maximum of "9" points from the skill checklist.

    4 weeks

Secondary Outcomes (4)

  • The state trait anxiety scale

    3 weeks

  • self efficacy scale

    3 weeks

  • perceived learning scale

    3 weeks

  • Student satisfaction and self-confidence in learning scale

    1 weeks

Study Arms (2)

Experimental

EXPERIMENTAL

49 students in the experimental group experienced the ability to prepare a school-age child for the procedure with a simulation using standardized pediatric patients.

Other: simulation with standardized child patient

Control

NO INTERVENTION

No attempt was made to the students in the control group.

Interventions

49 students in the experimental group experienced the ability to prepare a school-age child for the procedure with a simulation using standardized pediatric patients. In the simulation, a school-aged child was used as the standard patient.

Experimental

Eligibility Criteria

Age20 Years - 22 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Being a 3rd year student of Health Sciences University Gülhane Nursing Faculty
  • To be taking the Child Health and Diseases Nursing course for the first time
  • Agree to participate in the research
  • Being a Turkish citizen and able to speak and understand Turkish

You may not qualify if:

  • Being a foreign student
  • To have taken the Child Health and Diseases Nursing course before
  • Refusing to participate in the research

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Health Sciences University

Ankara, 0618, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

Study Officials

  • Hülya ZENGIN

    Yuksek Ihtisas University

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: The research was carried out using a convergent parallel design, which is a mixed method, which includes a randomized controlled study with a pretest-posttest control group, which is one of the quantitative research methods, and a phenomenological approach, one of the qualitative research designs.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant professor

Study Record Dates

First Submitted

December 19, 2022

First Posted

January 5, 2023

Study Start

November 5, 2019

Primary Completion

November 25, 2019

Study Completion

December 31, 2019

Last Updated

January 5, 2023

Record last verified: 2023-01

Data Sharing

IPD Sharing
Will not share

Locations