- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05596487
The Effect of Repetitive Standardized Patient Simulation and End of Life Care Education on Nursing Students' Knowledge Attitudes and Moods
October 29, 2022 updated by: Betül Çakmak, Ankara Yildirim Beyazıt University
The Effects of End of Life Care Education and Repetitive Standard Patient-Based Simulation on Nursing Students' Knowledge Level, Attitudes and Moods Towards the Patient With Dying Process
This research is a randomized experimental intervention study designed to examine the effect of repetitive standard patient-based education given to nursing students with end-of-life care education nursing on the level of knowledge, attitudes, and moods of the patient's care during the death process.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The research Sample of the study consisted of fourth-year nursing students who agreed to participate in the study (n=50).
In the study, an end-of-life care nursing education program was applied to all students.
In the second stage, the standard patient-based practice was performed once with the control group nursing students and twice with the intervention group students.
In data collection, an end-of-life care nursing questionnaire, Frommelt attitude scale, positive-negative affect scale, and modified simulation effectiveness tool were used.
Study Type
Interventional
Enrollment (Actual)
50
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
-
-
-
Ankara, Turkey, 06010
- Ankara Yıldırım Beyazıt University, Faculty of Health Sciences, Department of Nursing
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Not having a course in which a four-year undergraduate education is unsuccessful,
- Not participating in the pilot study of the research
- To voluntarily agree to participate in the research.
- Being a fourth-year student in the Department of Nursing
Exclusion Criteria:
- Participating in the pilot study of the research
- Wanting to leave the research.
- Being a first, second and third-year student in the Department of Nursing
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: experimental: repetitive standardized patient simulation
In the study, an end-of-life care nursing education program was applied to all students.
In the second stage, the standard patient-based practice was performed once with the control group nursing students and twice with the intervention group students.
|
In the study, an end-of-life care nursing education program was applied to all students.
In the second stage, the standard patient-based practice was performed once with the control group nursing students and twice with the intervention group students.
In data collection, an end-of-life care nursing questionnaire, Frommelt attitude scale, positive-negative affect scale, and modified simulation effectiveness tool were used.
|
|
No Intervention: control grup
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge level on end-of-life care nursing
Time Frame: 21 Days
|
Evaluated with an end-of-life care nursing questionnaire.
This form was developed by the researcher.
students answered the test exam.
The exam consists of 25 questions.
Minimum point is "0" and the maximum point is "100".
The higher the score, the higher the knowledge level of the end of life care.
|
21 Days
|
|
Attitude score toward the care of the patient during the death process
Time Frame: 21 Days
|
Evaluated with the scale of Attitude Towards Caring for Dying Patients.
Minimum point is "30" and the maximum point is "150".
The higher the score, the higher the positive attitude.
|
21 Days
|
|
positive-negative mood level
Time Frame: 21 Days
|
Evaluated with Positive and negative affect:The PANAS Scales-PANAS.
It includes 20 emotions, including 10 positive affect and 10 negative affect.
It is evaluated in a 5-point Likert type and indicates that the emotion is felt as 1 = very little or not at all, 5 = very much.
|
21 Days
|
|
evaluate the effectiveness of the simulation environment
Time Frame: 21 Days
|
Evaluated with Simulation Effectiveness Tool-Modified.
Minimum point is "18" and the maximum point is "95".
The higher the score, the higher the positive perception of the learning activity.
|
21 Days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 26, 2022
Primary Completion (Actual)
March 19, 2022
Study Completion (Actual)
March 19, 2022
Study Registration Dates
First Submitted
October 24, 2022
First Submitted That Met QC Criteria
October 24, 2022
First Posted (Actual)
October 27, 2022
Study Record Updates
Last Update Posted (Actual)
November 2, 2022
Last Update Submitted That Met QC Criteria
October 29, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 15.03.2021
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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