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medRxiv preprint doi: https://doi.org/10.1101/2024.09.20.24314075; this version posted September 24, 2024. The copyright holder for this preprint (which was not certified by peer review) is the author/funder,
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How to fill out validation of a difference-in-differences

01
Define your treatment and control groups.
02
Collect pre-intervention data for both groups to establish a baseline.
03
Ensure parallel trends in pre-intervention periods using statistical tests or visual inspections.
04
Conduct the difference-in-differences analysis by comparing the changes over time between the treatment and control groups.
05
Validate your findings with robustness checks, such as placebos or alternative specifications.
06
Document any assumptions made in your analysis for transparency.

Who needs validation of a difference-in-differences?

01
Researchers conducting policy evaluations.
02
Academics working in economics or social sciences.
03
Organizations assessing the impact of an intervention.
04
Government agencies evaluating the effects of legislation.
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Validation of a difference-in-differences is a statistical technique used to confirm the credibility and reliability of causal inferences made from observational data by comparing the changes in outcomes over time between a treatment group and a control group.
Researchers and analysts conducting empirical studies that utilize difference-in-differences as their methodological framework are typically required to file a validation of their findings to ensure the robustness of their statistical analysis.
To fill out validation of a difference-in-differences, you should provide an overview of your study design, detail your data sources, specify the treatment and control groups, describe your methodological approach, and include statistical tests performed to validate the model.
The purpose of validation of a difference-in-differences is to demonstrate that the estimated treatment effects are reliable, to rule out alternative explanations for the observed effects, and to provide transparency regarding the analysis conducted.
The information that must be reported includes the sample size, outcome metrics, treatment and control group characteristics, key assumptions made in the analysis, and results from any supplementary robustness checks.
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