Informed consent: Informed consent is the process of obtaining voluntary agreement from participants after providing them with all relevant information about the study, including potential risks and benefits.
Institutional Review Board (IRB): An IRB is a committee that reviews research proposals to ensure they meet ethical standards and protect the rights and welfare of human participants.
Debriefing: Debriefing involves providing participants with additional information about the study after their participation, addressing any concerns or questions they may have.