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Article online verffentlicht: 22.12.2023 ThiemeOriginal ArticleEstimation of Influenza Vaccine Effectiveness using Secondary Data: A Cohort Study and Propensity Scratched Analysis of Claims Data from
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01
Start by gathering all the necessary information about the cohort
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Begin by filling out the basic details such as the name of the cohort and the purpose of the database
03
Include information about the inclusion and exclusion criteria for the cohort
04
Fill out the demographic information such as age, gender, race, etc. for each individual in the cohort
05
Include variables related to the specific research question or objective of the cohort database
06
Make sure to document any methodologies used for data collection and data quality assurance
07
Include any additional information or variables that might be relevant for future analysis
08
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Who needs protocol for cohort database?

01
Researchers conducting cohort studies
02
Healthcare professionals managing patient data
03
Institutions or organizations conducting population health research
04
Government agencies collecting and analyzing epidemiological data
05
Public health researchers studying long-term health outcomes
06
Pharmaceutical companies conducting clinical trials
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The protocol for a cohort database is a formal document that outlines the study design, objectives, methodology, and operational details for data collection and management within the cohort study.
Researchers, institutions, or organizations conducting studies that involve cohort databases are required to file the protocol.
To fill out the protocol for a cohort database, researchers should provide details regarding the study objectives, participant selection criteria, data collection methods, and analysis plan, ensuring all sections of the protocol template are completed thoroughly.
The purpose of the protocol for a cohort database is to ensure the research is conducted ethically and systematically, providing clear guidelines for data collection and analysis to maintain the integrity of the study.
Information required includes study objectives, participant demographics, inclusion and exclusion criteria, data collection methods, analytical methods, and timelines.
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