- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04136691
The Effect of Simulation Method on Nursing Students' Burn Patient Care Planning
October 22, 2019 updated by: Müjgan ONARICI, Çankırı Karatekin University
The Effect of Simulation Method on Nursing Students' Burn Patient Care Planning:a Randomized Controlled Trial
Aim: This research was conducted as a single-blind randomized control group intervention trial to determine the effectiveness of simulation method performed using high-fidelity human patient simulator in nursing students' burn patient care planning.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Materials and Methods: The research was carried out with randomly-selected 61 students including 31 in intervention and 30 in control groups who took the Surgical Diseases Nursing Course in the spring term of the 2017-2018 academic year.
The research data were collected using "Personal Information Form", "Cognitive Level Assessment Test for Burn Patient Care", "The Student Satisfaction and Self-Confidence in Learning Scale", "Simulation Design Scale", "Educational Practices Questionnaire", and "Evaluation Form for Burn Patient Care Plan".
In the application process of the research, knowledge tests were administered as a pretest, second test, and posttest, and first and second applications of burn patient care plans were performed with all students.
In the research, the application of burn patient scenario was performed only with the intervention group.
Descriptive statistics, Chi-Square, Mann-Whitney U Test, and Wilcoxon Sign Test were used to analyze the data.
Study Type
Interventional
Enrollment (Actual)
61
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Çankırı, Turkey, 18200
- Çankırı Karatekin University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 27 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Enrolled in the course
- Had not taken this course and any training on burn patient care before
- Accepted to participate in the research
Exclusion Criteria:
- Have any records of absence
- Taken this course and training on burn patient care before
- Graduate of health vocational high school
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: simulation training
In the application process of the research, knowledge tests were administered as a pretest, second test, and posttest, and first and second applications of burn patient care plans were performed.
In the research, the application of burn patient scenario was performed only with the intervention group.
|
Burn patient scenario was performed with the intervention group.
|
|
No Intervention: Control
In the application process of the research, knowledge tests were administered as a pretest, second test, and posttest, and first and second applications of burn patient care plans were performed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Differences of knowledge scores between groups
Time Frame: The first knowledge test was conducted in the first week, the second knowledge test in the fourth week (1 week after simulation application) and the third knowledge test in the fifth week. Total duration 5 weeks.
|
First, second and third knowledge tests were applied to measure the level of knowledge.
|
The first knowledge test was conducted in the first week, the second knowledge test in the fourth week (1 week after simulation application) and the third knowledge test in the fifth week. Total duration 5 weeks.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Differences of nursing interventions scores between groups
Time Frame: The first burn patient care plan was implemented in the second week and the second care plan in the fifth week (2 weeks after simulation application).
|
The first and second burn patient care plans were applied to measure the level of care planning.
|
The first burn patient care plan was implemented in the second week and the second care plan in the fifth week (2 weeks after simulation application).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Aqel AA, Ahmad MM. High-fidelity simulation effects on CPR knowledge, skills, acquisition, and retention in nursing students. Worldviews Evid Based Nurs. 2014 Dec;11(6):394-400. doi: 10.1111/wvn.12063. Epub 2014 Sep 11.
- Onarıcı M, Karadağ M. The Effect of Simulation Method on Nursing Students' Burn Patient Care Planning: A Randomized Controlled Trial. J Burn Care Res. 2021 Sep 30;42(5):1011-1016. doi: 10.1093/jbcr/irab018.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 19, 2018
Primary Completion (Actual)
March 6, 2018
Study Completion (Actual)
April 12, 2018
Study Registration Dates
First Submitted
October 16, 2019
First Submitted That Met QC Criteria
October 22, 2019
First Posted (Actual)
October 23, 2019
Study Record Updates
Last Update Posted (Actual)
October 23, 2019
Last Update Submitted That Met QC Criteria
October 22, 2019
Last Verified
October 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Cankırı KU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
IPD Plan Description
in progress
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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