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The Effect of Hybrid Simulation on Evaluating Neonatal Jaundice

Primary Purpose

Nursing Education

Status
Recruiting
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
simulation training
Sponsored by
Çankırı Karatekin University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Nursing Education focused on measuring Nursing education, hyperbillirubinemia, simulation

Eligibility Criteria

19 Years - 27 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Enrolled in the course Had not taken this course before Accepted to participate in the research Exclusion Criteria: Have any records of absence Taken this course before Graduate of health vocational high school

Sites / Locations

  • Çankırı Karatekin ÜniversitesiRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention/Treatment

Control

Arm Description

In the implementation process of the research, knowledge tests will be applied as pre-test and post-test, and training will be given to the mother who has a baby with physiological jaundice. In the study, the scenario of the mother with a baby with jaundice will be implemented only with the intervention group

During the application process of the research, knowledge tests will be applied as pre-test and post-test.

Outcomes

Primary Outcome Measures

Student Information Form and First Knowledge Test
Student Information Form (First Knowledge Test-Before Simulation): In this form, which was created by the researcher by scanning the literature, did he choose the student's number, age, gender, graduated high school, nursing department willingly, did he get information about the simulation before, did he get information about neonatal jaundice? ? The questions are included. In the same survey, there is the "Newborn Physiological Jaundice Assessment Test" consisting of 25 questions created by the researchers. In this questionnaire, there are statements regarding the physiological jaundice of the newborn. Students were asked to mark one of the options "Yes", "No" or "I don't know" for these statements. This form was applied to the students as a pre-test. After the pretest, the subject was explained about the physiological jaundice of the newborn. This form was filled by both the experimental and control groups.
Jaundice case checklist form
Jaundice case checklist form (During simulation): This checklist was created by the researcher. There are statements for learning objectives set to evaluate neonatal jaundice. These expressions are "did", "did not" and "partially did". The behavior of the student during the simulation was evaluated by the researcher and his peers. After the simulation, the student was asked to evaluate himself on this form and fill out the form.
Second Student Knowledge Test
Second Student Knowledge Test (After the Simulation): 2 weeks after the simulation application, the "Newborn Physiological Jaundice Assessment Test" was applied to both the control and experimental groups. In addition to this test, "Student Satisfaction and Self-Confidence Scale in Learning" and "Simulation Design Scale" were applied to the experimental group.

Secondary Outcome Measures

Full Information

First Posted
December 5, 2022
Last Updated
January 3, 2023
Sponsor
Çankırı Karatekin University
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1. Study Identification

Unique Protocol Identification Number
NCT05677477
Brief Title
The Effect of Hybrid Simulation on Evaluating Neonatal Jaundice
Official Title
The Effect of Hybrid Simulation on Nursing Students' Ability to Evaluate Neonatal Physiological Jaundice: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 20, 2022 (Actual)
Primary Completion Date
December 20, 2022 (Actual)
Study Completion Date
March 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Çankırı Karatekin University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study will be conducted as a single-blind randomized control group intervention trial to determine the effectiveness of the hybrid simulation method using standard patient and low-fidelity baby simulators in the intervention of nursing students for neonatal physiologic jaundice.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nursing Education
Keywords
Nursing education, hyperbillirubinemia, simulation

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
Single blind
Allocation
Randomized
Enrollment
72 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention/Treatment
Arm Type
Experimental
Arm Description
In the implementation process of the research, knowledge tests will be applied as pre-test and post-test, and training will be given to the mother who has a baby with physiological jaundice. In the study, the scenario of the mother with a baby with jaundice will be implemented only with the intervention group
Arm Title
Control
Arm Type
No Intervention
Arm Description
During the application process of the research, knowledge tests will be applied as pre-test and post-test.
Intervention Type
Other
Intervention Name(s)
simulation training
Intervention Description
A mother scenario with a baby with physiological jaundice will be implemented with the intervention group.
Primary Outcome Measure Information:
Title
Student Information Form and First Knowledge Test
Description
Student Information Form (First Knowledge Test-Before Simulation): In this form, which was created by the researcher by scanning the literature, did he choose the student's number, age, gender, graduated high school, nursing department willingly, did he get information about the simulation before, did he get information about neonatal jaundice? ? The questions are included. In the same survey, there is the "Newborn Physiological Jaundice Assessment Test" consisting of 25 questions created by the researchers. In this questionnaire, there are statements regarding the physiological jaundice of the newborn. Students were asked to mark one of the options "Yes", "No" or "I don't know" for these statements. This form was applied to the students as a pre-test. After the pretest, the subject was explained about the physiological jaundice of the newborn. This form was filled by both the experimental and control groups.
Time Frame
One week before Simulation (First week)
Title
Jaundice case checklist form
Description
Jaundice case checklist form (During simulation): This checklist was created by the researcher. There are statements for learning objectives set to evaluate neonatal jaundice. These expressions are "did", "did not" and "partially did". The behavior of the student during the simulation was evaluated by the researcher and his peers. After the simulation, the student was asked to evaluate himself on this form and fill out the form.
Time Frame
During simulation (Second week)
Title
Second Student Knowledge Test
Description
Second Student Knowledge Test (After the Simulation): 2 weeks after the simulation application, the "Newborn Physiological Jaundice Assessment Test" was applied to both the control and experimental groups. In addition to this test, "Student Satisfaction and Self-Confidence Scale in Learning" and "Simulation Design Scale" were applied to the experimental group.
Time Frame
Two weeks after simulation (Fourth week)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
27 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Enrolled in the course Had not taken this course before Accepted to participate in the research Exclusion Criteria: Have any records of absence Taken this course before Graduate of health vocational high school
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aylin Pekyiğit
Phone
05396506489
Email
aylinpekyigit@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Müjgan Onarıcı
Organizational Affiliation
Çankırı Karatekin University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Tuğba Yıldırım
Organizational Affiliation
Çankırı Karatekin University
Official's Role
Study Chair
Facility Information:
Facility Name
Çankırı Karatekin Üniversitesi
City
Çankiri
ZIP/Postal Code
18200
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aylin Pekyiğit
Phone
05413528050

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
25030974
Citation
Choi YJ. Exploring experiences of psychiatric nursing simulations using standardized patients for undergraduate students. Asian Nurs Res (Korean Soc Nurs Sci). 2012 Sep;6(3):91-5. doi: 10.1016/j.anr.2012.07.001. Epub 2012 Jul 20.
Results Reference
background

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The Effect of Hybrid Simulation on Evaluating Neonatal Jaundice

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