Potential risks refer to the possibility of harm or negative consequences that may arise during a study or experiment. These risks can include physical, psychological, or emotional harm to participants.
Related terms
Informed Consent: Participants are fully informed about the potential risks involved in the study before they decide whether or not to participate.
Institutional Review Board (IRB): A committee responsible for reviewing and approving research studies to ensure ethical standards are met and potential risks are minimized.
Debriefing: After participating in a study involving potential risks, participants are provided with information about the purpose of the study and any necessary support or resources.