refers to deliberatelymisleading or falsely informing participants about the nature of the research.
some forms of deception are less harmful than others and are necessary tomaintainthevalidity of a study.
it may be necessary to deceive participants through omission of information.
valid consent
giving participants enough information (in a form they can understand,) so that they can make an informed choice about whether they wish to participate.
if a participant is deceived, they automatically failtoprovidevalid consent, as they don't have enough information to make an informed choice.
confidentiality
ensuring that third parties are not able to trace information back to an individual participant.
risks of stress, anxiety, humiliation or pain
occurs in instances where research could induce more than minimal pain through repetitive or prolonged testing.
invasive testing, such as the administration of drugs, or vigorous physical excercise, would not usually be encountered in everyday life and is unethical as a result.
risk to the participant's values, beliefs, relationships or privacy
research that is likely to face this type of risk focuses on socially sensitive topics (e.g. sexuality, gender.)
(risk to ppt's values) this can also include breaches in confidentiality, such as showing participants without valid consent to do so.
vulnerable individuals
vulnerable individuals face greater risks than other participants as the psychologistholdsaposistionofpower over these participants, and as such they are subject to closer safeguarding measures.
vulnerable individuals are granted additionalprotections, through ethical guidelines and their use in psychologicalresearch is restricted.
examples of vulnerable individuals include:
children under 16
those lacking in mental capacity
people in care
people in custody or on probation
people engaged in illegal activities such as drug use
working with animals
ethical guidelines for working with animals were first introduced in the UK in 1968 as part of the Animals Act.