- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05040672
Evaluation of Knowledge and Practice About Prostate Cancer in Male Employees (LB2008)
July 29, 2022 updated by: Libbs Farmacêutica LTDA
Evaluation of Knowledge and Practice About Prostate Cancer in Male Employees of Libbs Pharmaceuticals
Analyze, through an online questionnaire, the knowledge and practice about the prevention and detection of prostate cancer in male employees of a pharmaceutical company.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In Brazil, there are still few published and current studies that explore man's attention and awareness of health.
Historically, women attend medical appointments and perform routine tests more frequently than men.
For this is very important Analyze, through an online questionnaire, the knowledge and practice about the prevention and detection of prostate cancer in male employees of Libbs Farmacêutica (a pharmaceutical company in Brazil).
Study Type
Observational
Enrollment (Actual)
280
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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-
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São Paulo, Brazil, 01140050
- Augusto Figueiredo
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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
Yes
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
As this is a non-probabilistic or convenience (non-random) sampling, the sample size calculation is not applicable.
Today there are about 1500 male employees at Libbs Pharmaceuticals and all will be invited to participate in the survey.
Answers obtained from all questionnaires filled in their entirety will be included for analysis.
Description
Inclusion Criteria:
- Male individuals included in the Libbs workforce;
- Age 18 years or older;
- Subjects who agree to participate in the study after reading and signing the Informed Consent Form.
Exclusion Criteria:
- There is no exclusion criteria
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Group I
All volunteer male employees of Libbs Pharmaceuticals residing in all Brazilian regions will participate in this research.An online questionnaire will be applied to assess research subjects understanding of prostate cancer and health habits.
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questionare online application
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Evaluation of Knowledge and Practice About Prostate Cancer e Healthy Habits
Time Frame: 1 month
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Assess the subjects knowledge and practice in relation to educational campaigns aimed at prostate cancer.All the information wil be collected using a questionnaire previously approved by the ethics committee.
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1 month
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
June 1, 2021
Primary Completion (Actual)
July 29, 2022
Study Completion (Actual)
July 29, 2022
Study Registration Dates
First Submitted
August 30, 2021
First Submitted That Met QC Criteria
September 3, 2021
First Posted (Actual)
September 10, 2021
Study Record Updates
Last Update Posted (Actual)
August 2, 2022
Last Update Submitted That Met QC Criteria
July 29, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LB2008
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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