- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05411172
Evaluation of a Model-Based CBRN Training Program (CBRN)
February 19, 2024 updated by: Derya Aslan Huyar, Uludag University
The Effect of Chemical Biological Radiological and Nuclear Training Program Based on Mastery Learning Model on the Learning Outcome of Student Nurses
The aim of the study is to evaluate the effect of the Education Program based on the Mastery Learning Model for Chemical, Biological, Radiological, and Nuclear threats and hazards (MLM-CBRN Education Program) on student nurses' knowledge, attitude, self-efficacy, and skill development in chemical, biological, radiological and nuclear threats and hazards.
The complete experimental design type was used in the study.
Study Overview
Status
Completed
Detailed Description
The aim of the study is to evaluate the effect of the Education Program based on the Mastery Learning Model for Chemical, Biological, Radiological, and Nuclear threats and hazards (MLM-CBRN Education Program) on student nurses' knowledge, attitude, self-efficacy, and skill development in chemical, biological, radiological and nuclear threats and hazards.
The complete experimental design type was used in the study.
The study sample comprised 104 4th-year nursing students (52 in the experimental group, 52 in the control group).
The MLM-CBRN Education Program was carried out with the students in the experimental group face-to-face as theoretical and practical education once a week for four weeks.
As a criterion for starting a new unit, 80% of the participants needed to receive minimum 70 points from the unit follow-up tests in line with the "Learning Objective" determined within the scope of the Mastery Learning Model.
The data were collected before and right after the intervention and in the 1st and 3rd months after the intervention using the "Personal Information Form," "Nursing Student CBRN Knowledge Test," "Nursing Student CBRN Attitude Scale," and "Nursing Student CBRN Self-Efficacy Scale."
Moreover, only the knowledge scores of the students in the experimental group were collected using the unit follow-up tests, which enabled us to check whether the "Learning Objective" related to the unit taught was achieved.
During the skill training, the "START Triage and JumpSTART Triage Skill Check List," Gas Mask Wearing-Removing Skill Check List, and Level C Clothes Wearing-Removing Skill Check List were scored for each student in the experimental group after observing the students twice.
Study Type
Interventional
Enrollment (Actual)
104
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
-
-
Nilüfer
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Bursa, Nilüfer, Turkey, 16285
- Bursa Uludağ Üniversitesi
-
-
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
20 years to 30 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being a senior nursing undergraduate student
- Not having received CBRN training
Exclusion Criteria:
- Be a full-time worker in a healthcare institution
- Having taken courses on disaster and CBRN
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 |
|---|---|
|
No Intervention: Control
No intervention
|
|
|
Experimental: Experimental
The Effect of the Education Based on the Mastery Learning Model on the Practical Skills of Student Nurses in Chemical, Biological, Radiological, and Nuclear Hazards. The MLM-CBRN Education Program was carried out with the students in the experimental group face-to-face as theoretical and practical education once a week for four weeks. |
The MLM-CBRN Education Program was carried out with the students in the experimental group face-to-face as theoretical and practical education once a week for four weeks. .
The data were collected before and right after the intervention and in the 1st and 3rd months after the intervention using the "Personal Information Form," "Nursing Student CBRN Knowledge Test," "Nursing Student CBRN Attitude Scale," and "Nursing Student CBRN Self-Efficacy Scale."
Moreover, only the knowledge scores of the students in the experimental group were collected using the unit follow-up tests, which enabled us to check whether the "Learning Objective" related to the unit taught was achieved.
During the skill training, the "START Triage and JumpSTART Triage Skill Check List," Gas Mask Wearing-Removing Skill Check List, and Level C Clothes Wearing-Removing Skill Check List were scored for each student in the experimental group after observing the students twice.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Individual Information Form
Time Frame: up to 24 weeks
|
It consists of items questioning the students' demographic data, their school success, and whether they have received a CBRN education or not.
|
up to 24 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Nursing Student CBRN Knowledge Test
Time Frame: up to 24 weeks
|
Knowledge Test used to determine the knowledge level of nursing students about CBRN consists of 31 items.
The answer options of true and false statements.
The score that can be obtained from the test varies between 0-31.
The results get improve as the points are received.KR-20 was calculated as 0.82
|
up to 24 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Nursing Student CBRN Attitude Scale
Time Frame: up to 24 weeks
|
To determine their attitudes about kbrn used it.Attitude Scale.
The scale consists of 3 sub-factors.
Individual attitude (factor 1), professional attitude (factor 2), and social attitude (factor 3).
Scores related to the scale score and sub-dimensions are obtained by adding the scores given to the items and dividing them by the number of items.
It is a Likert-type scale and is graded between "5" completely agree and "1" strongly disagree.
The Cronbach Alpha is 0.92.
The score that can be obtained from the test varies between 1-5.
The results get improve as the points are received.
|
up to 24 weeks
|
|
Nursing Student CBRN Self-Efficacy Scale
Time Frame: up to 24 weeks
|
To determine their self-efficacy about kbrn used it.
The Self-Efficacy Scale score is obtained by adding the scores given to the items and dividing them by the number of items.
The CBRN attitude scale was grouped under a single factor structure.
The scale consists of 9 items.
Scores from the scale range from 1 to 5. It is a Likert-type scale.
The Cronbach Alpha is 0.90.
The score that can be obtained from the test varies between 1-5.
The results get improve as the points are received.
|
up to 24 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: Melek Nihal Esin, mnesin@istanbul.edu.tr
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)
January 1, 2020
Primary Completion (Actual)
February 20, 2020
Study Completion (Actual)
March 12, 2020
Study Registration Dates
First Submitted
December 16, 2021
First Submitted That Met QC Criteria
June 5, 2022
First Posted (Actual)
June 9, 2022
Study Record Updates
Last Update Posted (Actual)
February 20, 2024
Last Update Submitted That Met QC Criteria
February 19, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 982d71uk
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
if requested; training plan, data collection forms used, presentation content used, checklists used, unit follow-up tests used, and case examples used can be shared.
IPD Sharing Time Frame
1-12 months
IPD Sharing Access Criteria
have ethics committee approval, Researchers who want to do meta-analysis or systematic review
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
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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