Common concerns about sharing human subject research data include:
The release of information that may identify an individual research participant or organization. Examples of disclosive information include:
An individual's control over the extent, timing, and circumstances of sharing oneself (physically, behaviorally, or intellectually) with others. In a research context, the concerns are primarily about the methods used to obtain information about subjects.
The treatment of information disclosed in a relationship of trust with the expectation that it will not be divulged without permission.
Restrictions that apply to some types of sensitive data. Examples include:
Any information that may cause harm, legal jeopardy, or reputational damage to the subject if disclosed. This data may or may not be legally protected. Examples include:
Visit the Office of Research Compliance's Human Research Protection Program site for information on research that involves human subjects. To determine whether an IRB application is required for your project, complete the tutorial "Does my project require IRB Approval?" or contact the HRPP at firstname.lastname@example.org or (662) 325-3994.
For projects that require IRB approval, the informed consent should maintain participant confidentiality without overly restricting future use of the data. Overly restrictive language will make future sharing or archiving of the data more difficult or impossible later.
If your data contains legally protected or sensitive data, or if the removal of identifiers limit the usefulness of your data, consider sharing through archives with restricted access repositories, such as the Inter-University Consortium for Political and Social Research (ICPSR).
In addition to the content of the data, the agreement made with participants in your IRB can also limit the extent to which human subjects' data can be shared.