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informed consent
a process in which potential participants are informed about what participation in the study will involve, so that they can make an informed decision whether or not to engage in the research
debriefing
a session following participation in a study, in which the participants are informed of the true purpose of the research
contamination
a result of communication among members of a research participant pool, the effects of debriefing-generated suspicion may extend beyond those who have participated in deception experiments
process debriefing
An extensive form of debriefing, particularly when the experimental manipulation has involved providing false information of some kind about the participant’s personality, competence, or self- esteem
Suggestions for participant safety in a dataset
only objective information be included in the dataset
individuals be given the right to review their files for accuracy, and to have errors corrected
files of individuals be identified only by code numbers, with access to personal identification strictly restricted
security precautions be instituted for screening data users and restricting access
linking system
a mediating step between access to a particular file and connection between file number and person’s name
Common Rule
federal regulations regarding the conduct of research involving human participants
institutional review board
committee that evaluates, approves, and monitors all research projects in an institution with respect to ethical requirements and practices
Components reviewed in the IRB
consent form and debriefing procedures
participant recruitment and characteristics
methods and measures
potential risks and benefits to participants
precautions to safeguard data