What must social workers obtain to report research findings with identifying information?

The requirement for social workers to obtain proper consent from participants before reporting research findings that include identifying information is rooted in ethical standards and the principles of confidentiality and respect for individuals in research. Informed consent ensures that participants are fully aware of how their data will be used, what the implications of their participation are, and that they agree to the use of their personal information in the context of research reporting. This obligation is crucial for protecting the privacy and autonomy of individuals involved in the study, particularly in sensitive fields like social work where data may pertain to vulnerable populations.

Obtaining proper consent also aligns with institutional and legal regulations that govern research practices, ensuring that the rights of participants are upheld. Without such consent, it would be unethical and potentially harmful to disclose any identifying information, as it may jeopardize the participants' privacy and well-being.