What document is used to request the use or disclosure of health information in a research study?

The appropriate document used to request the use or disclosure of health information in a research study is a compound authorization. This document combines elements of informed consent and authorization for the use of protected health information (PHI) for research purposes. It ensures that individuals are fully informed about how their health data will be used and allows researchers to access the necessary information while complying with legal and ethical standards.

In the context of research involving human subjects, a compound authorization streamlines the process by allowing participants to consent to both the research study itself and the specific use or disclosure of their health information in one comprehensive document. This is particularly important for ensuring that participants are adequately informed about the implications of their participation and the processing of their personal health data.

While informed consent is essential for gaining approval from participants to take part in the study, it does not necessarily cover the specific use or disclosure of healthcare data unless it includes authorization elements. A data use agreement is typically utilized for sharing data between organizations but isn't specifically for individual authorization. The research protocol outlines the overall plan of the study, including methods and objectives, but does not serve as a document for requesting health information. Thus, the compound authorization is the correct document for this purpose.