How Does Informed Consent Relate to Data Confidentiality?
Informed consent is a foundational principle in epidemiological research that ensures participants are fully aware of how their data will be used and protected. Participants should be informed about:
1. Purpose of the Study: Why the data is being collected and how it will be used. 2. Data Protection Measures: Steps that will be taken to protect their confidential information. 3. Potential Risks: Any potential risks to their privacy and how these risks will be mitigated. 4. Rights: Their rights to access, amend, or withdraw their data from the study.
