Cardiovascular Disease Risk Factors Prevalence Among Bayer's Employees in São Paulo, Brazil
NCT ID: NCT02055651
Last Updated: 2016-11-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
361 participants
OBSERVATIONAL
2013-08-31
2016-10-31
Brief Summary
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Objective: Evaluate Bayer employees' cardiovascular health according to the AHA definition and the acceptance to engage in lifestyle change programs.
Methods: By the time of the annual occupational safety periodic medical examination, employees will receive an email with information about the cardiovascular health screening, exams requisition (fasting blood glucose and total cholesterol) and a copy of the written informed consent. If the employee accepts to participate, after providing a written informed consent, he will be evaluated according to the AHA cardiovascular health metrics. Data will be collected at the occupational safety electronic health record. After medical evaluation, employees will receive a printed feedback with their cardiovascular health score and will be referred to indicated lifestyle change programs (healthy weight, smoking cessation, diabetes control, high blood pressure control, dyslipidemia control).
After 12 months we will evaluate the percentage of employees who accept to participate; prevalence of the cardiovascular risk factors and distribution according to the AHA classification in ideal, intermediate and poor; adherence to lifestyle change programs.
Detailed Description
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Conditions
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Keywords
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Study Design
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ECOLOGIC_OR_COMMUNITY
PROSPECTIVE
Study Groups
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Bayer Sao Paulo employees
Workers from Bayer in site Socorro who participate in the trial
Examination and survey
Routine medical examination as required by law and follow-up for lifestyle change program
Interventions
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Examination and survey
Routine medical examination as required by law and follow-up for lifestyle change program
Eligibility Criteria
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Inclusion Criteria
* Provide written informed consent
Exclusion Criteria
* Employees that are retired from work during the study period
20 Years
ALL
Yes
Sponsors
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Bayer
INDUSTRY
Responsible Party
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Principal Investigators
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Bayer Study Director
Role: STUDY_DIRECTOR
Bayer
Locations
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São Paulo, , Brazil
Countries
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Other Identifiers
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NN1325BR
Identifier Type: OTHER
Identifier Source: secondary_id
17312
Identifier Type: -
Identifier Source: org_study_id