CITI Assessing Risk - SBE Practice Test 2025 – The Comprehensive All-in-One Guide to Master Risk Assessment

The primary goal of HIPAA (Health Insurance Portability and Accountability Act) in relation to research is to protect sensitive health information while allowing research to continue. HIPAA is designed to safeguard individuals' medical records and other personal health information from being disclosed without their consent or knowledge.

In the context of research, this means that while researchers can use health information to advance medical knowledge and improve patient care, they must do so in a way that ensures patient privacy and confidentiality are maintained. HIPAA sets forth privacy rules that govern how personal health information can be collected, stored, and shared for research purposes. It allows for the use of de-identified data, where individual identifiers are removed, enabling research to proceed without compromising personal privacy.

This balance is crucial as it supports the advancement of healthcare and scientific understanding while ensuring ethical standards regarding patient data are upheld. The other options either suggest limitations or prohibitions that do not align with HIPAA’s intended purpose of facilitating responsible research through appropriate protections of sensitive information.