part 1 Flashcards
what is a directional hypothesis?
previous research may have been done
can predict the results
IV affects the DV
what is a null hypothesis?
IV will not affect the DV
what is a non-directional hypothesis?
IV will affect the DV
can’t predict the results
what is a participant variable?
extraneous variable where the age; gender; intelligence; experience etc of the participant may affect the study
what is situational variable?
when the surrounding environment and experimental setting may affect the study
e.g. noise, time of day, lighting etc
what is a confounding variable?
vary systematically with the IV
occur when extraneous variables are not controlled
decrease the validity of results
what are demand characteristics?
cues that make participants guess the aim of the study (unintentionally) so they change their behaviour
what is the please-U effect?
over performing to please the researcher
what is the screw-U effect?
under performing to sabotage results
what is randomisation?
the use of chance where possible to reduce investigator effects
e.g. a memory test where participants have to recall a list of words. the order of the words should be randomly generated so the researcher does not have an influence over the order
what is standardisation?
when we keep everything the same (apart from the IV) for each participant
what is random allocation?
randomly assigning people to the different experimental conditions
what is ABBA counterbalancing?
balancing the order we do conditions in when using repeated measures
i.e. participants experience the conditions in one order, then in the reverse order
reduces fatigue effects and practice effects
what does DRIPP stand for?
deception right to withdraw informed consent protection from harm privacy
what is deception?
deliberately withholding information or misleading participants
can deceive participants if it will not cause any distress once they have been debriefed (in which the true aim of the study will be fully explained)
can deceive for medical or scientific reasons as well
what is the right to withdraw?
should know they can withdraw at any time, and know how to withdraw
should not feel obliged to continue with their participation
if they withdraw, all their data will also be removed
what is informed consent?
participants should know as much as possible about the procedure before they agree to do it in a briefing
should sign a consent form
made aware of their rights (to withdraw) and any risks
under 16s need parental permission, and consent cannot be gained if they are on drugs or mentally unfit etc
what is presumptive consent?
a similar group of people are told about the study and asked if they are willing to take part. if they agree it is presumed that the real participants would too
what is prior general consent?
participants give their permission to take part in a number of studies, including at least one that will involve deception
if they agree to do this then they agree to be deceived
what is retrospective consent?
participants are asked for their consent at the end of they study in the debriefing
they may not be aware they had taken part or may originally have been deceived
what is protection of participants (from harm)?
must be protected form physical and psychological harm, including embarrassment, feeling pressured or inadequate
participants should not be at any more risk than they would be in their everyday lives
participants should leave the study in the same state they arrived in
what is privacy (and confidentiality)?
data should not be shared unless the participant agrees to it
personal data is protected under the data protection act, which participants should be told in the brief and debrief
data is anonymous, if personal data is needed then participants should be referred to using numbers or initials
participants can be observed in public places without their knowledge, but not in their own homes
what is included in a consent form?
introduction / greeting ‘dear participant’
explanation of the study without giving away the full aim
explanation of what they’ll be required to do
explanation of confidentiality
explanation of their right to withdraw
any other issues
signed and dated consent
what is included in a debrief form?
thank them for taking part in the study
explanation of the true aim and what they expect to find
remind them of confidentiality
remind them of their right to withdraw
let them know where to find further information (contact details)