- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06173479
Health Belief Model-Based Educational Intervention on Safe Pesticide Use and Biomarkers in Agricultural Workers (HeBSaPU)
Effect of a Health Belief Model-Based Educational Intervention (HeBSaPU) on Safe Pesticide Use Practices and Biomarkers in Greenhouse Agriculture Workers in Antalya, Turkey
Brief Summary:
Purpose: This clinical trial aims to investigate the effect of educational interventions (HeBSaPU) based on the Health Belief Model on safe pesticide use and biomarkers among greenhouse agricultural workers. The main questions it aims to answer are;
- Compared to the control group, HeBSaPU affects safe pesticide use practices in greenhouse agricultural workers.
- Compared to the control group, HeBSaPU affects safe pesticide use health beliefs in greenhouse agricultural workers.
- Compared to the control group, HeBSaPU affects pesticide exposure determined by urine samples in greenhouse agricultural workers.
Participants took educational interventions based on Health Belief Model (HBM) sub-dimensions; including educational posters, free personal protective equipment (PPE) incentives, short reminder messages, and demonstration components about correct PPE usage.
Study Overview
Status
Intervention / Treatment
Detailed Description
The study aims to determine the effect of Health Belief Model (HBM) based educational interventions on safe pesticide use practices and biomarkers in greenhouse agricultural workers in Antalya, Turkey.
This research is a single-blind (participants), superiority randomized controlled trial design with a parallel group. The population of the research will be the greenhouse agricultural workers in the Sarıcasu Village of Antalya Province. In determining the research sample, the "effect of educational interventions on the change in protection behavior" was taken as Hegges g=0.89, and the sample number was calculated as 56 individuals with a 5% type 1 error margin. Considering that there would be losses during the research, it was planned to take 15-20% more of the sample (n=66).
On the map obtained from the Geographical Information Systems of Sarıcasu village, the greenhouses were randomized as experimental and control groups with the help of Randomizer.org.
Safe Pesticide Use Practices questionnaire, and Safe Pesticide Use Behaviors Health Belief Model Scale will be used to collect data. The variation of individuals' pesticide exposures will be determined by residue determination in urine samples.
Pre-testing of the study, taking the first urine samples, and starting the educational interventions will take place in the second week of November. At the end of twelve weeks, it is anticipated that the data collection process will be terminated with the collection of the last tests and the second urine samples in the last week of January.
At the end of the research, it is expected that the safe pesticide use behaviors of HBM-based education initiatives will change positively, and the diacyl phosphate metabolite concentrations in the urine will decrease with the effect of this change.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Konyaaltı
-
Antalya, Konyaaltı, Turkey, 07070
- Akdeniz University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Participant inclusion criteria
- Age: 18-65 years, inclusive
- Being a greenhouse agricultural worker
- Being a permanent employee in pesticide-related jobs in selected greenhouses,
- No communication-related barriers (language, speaking, understanding, etc.)
- Volunteering to participate in research
Participant exclusion criteria
- Being a seasonal agricultural worker
- Being a daily wage worker,
- Not dealing with pesticide-related works
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: HeBSaPU
HeBSaPU is an acronym for educational interventions for safe pesticide use based on the health belief model.
The HeBSaPU arm will get interventions for 12 weeks.
HeBSaPU include educational posters, free personal protective equipment (PPE) incentives, reminder short messages, and demonstration components about correct PPE usage.
|
HeBSaPU training content explains the definition of pesticides, their way of entry into the body, and their health effects.
Personal protective equipment, personal hygiene behaviors, and safe behaviors regarding the correct and safe use of pesticides were mentioned.
|
|
Active Comparator: Control
The control arm will not take any interventions.
|
HeBSaPU training content explains the definition of pesticides, their way of entry into the body, and their health effects.
Personal protective equipment, personal hygiene behaviors, and safe behaviors regarding the correct and safe use of pesticides were mentioned.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dialkylphosphates metabolites in urine samples
Time Frame: For 12-weeks
|
The concentration of four metabolites (Dimethyl phosphate, Diethyl phosphate, O,O-Dimethyl Dithiophosphate, O,O-Diethyl Dithiophosphate) is expected to change in urine samples.
|
For 12-weeks
|
|
Safe Pesticide Use Practice Level
Time Frame: For 12-weeks
|
Safe Pesticide Use Practice Questionare: A minimum of 20 and a maximum of 100 points are obtained from the questionnaire.
A higher total score means a higher pesticide safety level.
|
For 12-weeks
|
|
Health Beliefs for Safe Pesticide Use Practices
Time Frame: For 12-weeks
|
Health Belief Model Scale for Safe Pesticide Use Practices: A minimum of 39 and a maximum of 195 points are obtained from the scale.
An increase obtained from the scale is interpreted as a positive health belief level.
|
For 12-weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Dilan Akın, TUBİTAK
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- RCT829741
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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