- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05485389
The Effect of Simulation to Improve of Nurse's Attitudes Towards Elderly Patient
August 2, 2022 updated by: Istanbul Medipol University Hospital
The Effect of Simulation Based Learning on Improve Positive Attitudes and Individualized Care Perceptions of Nurses Towards Elderly Patient
The elderly population is increasing in the world.
Therefore, it is necessary to competent nurses who can diagnose the care needs of the elderly.
Trainings should be planned in order to improve nurses' perception of individualized care in the care and attitudes positively of elderly patient.
In post-graduate education, the use of traditional teaching methods and innovative simulation-based education will facilitate the increase of knowledge and skills.
The aim of this study is to examine the effect of simulation-based education on the improve of nurses' perception of individualized care and positive attitudes towards the elderly.
The study is quasi-experimental with a pre-test post-test design.
Before the data collection phase, a simulation-based training program consisting of three stages was created.
The data of the study were collected in a university hospital between October 2021 and April 2022, with the socio-demographic characteristics form, the perception of individualized care and the attitude scale towards the elderly.
The data will be analyzed in the package program and the study will be reported.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
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
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Bağcılar
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Istanbul, Bağcılar, Turkey
- Istanbul Medipol University Hospital
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Completed undergraduate education
- Have been working in the geriatric clinic for at least 6 months
- Volunteer to participate in the study
Exclusion Criteria:
- Not completing the stages of the study
- nurses with less than 6 months of experience in the geriatric clinic
- not volunteer to participate in the study
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: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Study group
At the beginning, knowledge test, individualized care perception and attitude scale to the elderly will be applied to the participants in the pre-test.
Then, 6-hour theoretical course on the care of the elderly patient will be given to the participants included in the study.
After the theoretical course, the knowledge test will be re-applied.
After that, experience will be provided within the scope of first, second and third level simulation-based learning, one week apart.
After the simulation experiences knowledge test, individualized care perception and attitude scale to the elderly will be applied to the participants in the post-test 1. Post-tests will be administered in the first (Post-test 2) and third (Post-test 3) months of the simulation experience.
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An educational methodology that aims to improve participants' attitudes towards the elderly and their perception of individualized care.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from attitudes towards the elderly at four months
Time Frame: Pre-test (before theoretical course), post test 1 (one week after simulation-based learning), post test 2 (one month after simulation-based learning) and post test 3(three month after simulation-based learning)
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Mean scores of the participants' on scale of attitude towards the elderly
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Pre-test (before theoretical course), post test 1 (one week after simulation-based learning), post test 2 (one month after simulation-based learning) and post test 3(three month after simulation-based learning)
|
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Change from perception of individualized care at four months
Time Frame: Pre-test (before theoretical course), post test 1 (one week after simulation-based learning), post test 2 (one month after simulation-based learning) and post test 3 (three month after simulation-based learning)
|
Mean scores of the participants on the scale of perception of individualized care for the elderly
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Pre-test (before theoretical course), post test 1 (one week after simulation-based learning), post test 2 (one month after simulation-based learning) and post test 3 (three month after simulation-based learning)
|
|
Change from knowledge test at four months
Time Frame: Pre-test (before theoretical course), immediately post test 1, post test 2 (one week after simulation-based learning), post test 3 (one month after simulation-based learning) and post test 4 (three month after simulation-based learning)
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Mean scores of the participants' on scale of knowledge of care towards the elderly
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Pre-test (before theoretical course), immediately post test 1, post test 2 (one week after simulation-based learning), post test 3 (one month after simulation-based learning) and post test 4 (three month after simulation-based learning)
|
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)
October 20, 2021
Primary Completion (Actual)
March 10, 2022
Study Completion (Actual)
April 10, 2022
Study Registration Dates
First Submitted
July 30, 2022
First Submitted That Met QC Criteria
August 2, 2022
First Posted (Actual)
August 3, 2022
Study Record Updates
Last Update Posted (Actual)
August 3, 2022
Last Update Submitted That Met QC Criteria
August 2, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 1122334455
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Plan Description
The study is a doctoral thesis.
It will first be reported as a thesis and then shared with the researchers as an article.
IPD Sharing Time Frame
The data will be used until the thesis and article process is completed.
IPD Sharing Supporting Information Type
- Clinical Study Report (CSR)
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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