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WHO/Institute Pasteur/IS ARIC/CONSIST Draft v1.13 26 January 2017 Disclaimer This document is a draft and the information contained herein is subject to change as this document is currently undergoing
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Step 1: Identify the research question or objective of the case-control study.
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Step 2: Define the study population by clearly defining the cases and controls.
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Step 3: Determine the source of cases and controls, such as hospitals, clinics, or registries.
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Step 4: Collect data on exposure or risk factors for each case and control.
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Step 5: Analyze the data using appropriate statistical methods, such as odds ratios or chi-square tests.
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Step 6: Interpret the results and draw conclusions based on the findings.
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Step 7: Communicate the findings through a research report or publication.

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Researchers and scientists conducting epidemiological studies.
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Healthcare professionals studying the causes of diseases.
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Public health officials aiming to assess the risk factors for certain health conditions.
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Policy makers looking to make informed decisions about public health interventions.
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Case-control study is a type of observational study in which two existing groups differing in outcome are identified and compared on the basis of some supposed causal attribute.
Researchers, epidemiologists, and healthcare professionals are required to file case-control studies.
Case-control studies are typically filled out by collecting data on exposure and outcome variables from study participants.
The purpose of a case-control study is to identify factors that may be associated with a particular health outcome.
Information on study design, study population, exposure variables, outcome variables, and statistical analysis methods must be reported on a case-control study.
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