The Effect of Toolbox Training on Radiation Protection Practices of Health Professionals in Radioactive Workplaces
The Effect of Toolbox Training on Radiation Protection Practices of Health Professionals Working in Radioactive Areas
Study Overview
Status
Intervention / Treatment
Detailed Description
This study will be conducted in a randomized controlled, pre-test, post-test and experimental group design to determine the effects of on-the-job training on radiation workers (radiation safety, protective clothing, awareness). The universe of the study was radiation workers using dosimeters at Hatay Mustafa Kemal University Health Practice and Research Hospital. The experimental group determined by randomization consisted of a total of 80 workers working in ionizing radiation departments. Data were collected with the Information Form, radiation safety and awareness Application Information Form (Pre-Test-Post-Test), radiation protection checklists and On-the-Job Training Evaluation Form. Descriptive statistical methods will be used in the evaluation of the data, independent sample t-test, dependent sample t-test will be used in the comparison of scores and the results of variance analysis in repeated measures will be used in the comparison of three follow-up scores.
The risk of cancer increases when exposed to medium and high doses of radiation (0.1 - 0.2 Gy), however, it is not clear whether the risk of cancer increases with acute low doses (0.1 Gy or lower) or low dose rates (1). Cancer risk is directly related to the absorbed dose. Therefore, it is important to create a model to define the effects of low radiation dose on carcinogenicity. In the report published in 2019, UNSCEAR (United Nations Scientific Committee on the Effects of Atomic Radiation) stated that the dose distributions and results arising from occupational exposure provide information about the source and conditions of exposure (2). This information has shown that the problems arising from radiation in departments working with ionizing radiation should be determined and further investigated. In addition, the protection of health professionals working in radioactive areas from radiation is important for both employee health and patient health. In particular, the implementation of the standards required for protection from radiation will emerge in this context and will provide protection from personal and institutional harm. In this context, it is very important for health professionals to address this issue more effectively in in-service training. In addition, it is thought that the time allocated by employees in environments such as hospitals, where the workload is high and the patient density is quite high, is quite limited and these personnel have little interest in in-service training provided with mass training methods. In this context, it is suggested that providing training to personnel with new training methods in environments such as hospitals will increase the permanence and impact of the training.
It is thought that this study will reveal the effects of new training methods on radiation protection practices of health workers working in radioactive areas, apart from mass training methods and routinely provided classical training methods, and will provide evidence for the use of this training method in addition to classical training methods.
10. Purpose of the study: The purpose of this randomized controlled, pre-test, post-test and experimental group design study is to provide on-the-job training to radiation officers working at Hatay Mustafa Kemal University Health Practice and Research Hospital and to investigate the effects of on-the-job training on radiation safety practices.
Place of the study: Hatay Mustafa Kemal University Health Practice and Research Hospital Universe and sample: The sample size of this study was determined using the simple random (randomized controlled) sampling method. It is planned to assign a total of 8 radioactive field workers who meet the sampling inclusion criteria to the experimental and control groups by drawing lots among the areas they work with the help of an external expert. It is planned that there will be a total of 80 radioactive field workers in the experimental and control groups to be assigned to the experimental and control groups as a result of the drawing lots, and 40 of this number will constitute the experimental group and 40 will constitute the control group.
Inclusion criteria:
- Working in radioactive areas
- Being a health professional
- Accepting to participate in the study voluntarily
Working for at least 6 months
12. The method planned to be used in the study: The universe of this study will consist of healthcare workers working in the radioactive areas of Hatay Mustafa Kemal University Health Practice and Research Hospital. The sample size of this study was determined using the simple random randomized controlled sampling method. It is planned to assign healthcare workers who meet the sampling inclusion criteria to experimental and control groups by drawing lots with the help of an external expert. According to the drawing results, experimental and control groups will be determined and on-the-job training will be given to the experimental group and radiation safety practices will be observed.
It is thought that this study will reveal the effects of new training methods other than mass training methods and routinely provided classical training methods on radiation protection practices of healthcare workers working in radioactive areas and will provide evidence for the use of this training method in addition to classical training methods.
Purpose of the study: The purpose of this randomized controlled, pre-test, post-test and experimental group design study is to provide on-the-job training to radiation officers working at Hatay Mustafa Kemal University Health Practice and Research Hospital and to investigate the effects of on-the-job training on radiation safety practices.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: BİRCAN KARA, Ph.D
- Phone Number: 05314505423
- Email: bircankara91@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Working in radioactive areas
- Being a health professional
- Agreeing to participate in the study voluntarily
- Working for at least 6 months
Exclusion Criteria:
- Working in any field other than radioactive areas
- Not being a health professional
- Working less than 6 months
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Toolbox trainings
Training given with a single page material, lasting between 10-15 minutes, aimed at on-the-job application.
|
Training given with a single page material, lasting between 10-15 minutes, aimed at on-the-job application.
|
|
No Intervention: control group
uninterrupted and monitored group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
pretest-posttest
Time Frame: before education and 1st week after training
|
It consists of 10 multiple choice questions created to measure the knowledge levels of the participants before and after the training.
|
before education and 1st week after training
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
radiation protection practices checklist
Time Frame: pre-training and post-training 1st week
|
Applications that form the basis of radiation protection applications consisting of 8 items
|
pre-training and post-training 1st week
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- hmkubircankara
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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