Research Methods Flashcards

1
Q

EXPERIMENTAL METHOD
What is an aim? What must it start with?

A

aim - the general statement that describes the purpose of the investigation
must start with ‘to investigate…’

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2
Q

EXPERIMENTAL METHOD
Define IV and DV

A

Independant variable = manipulated/changed
dependant variable = measured

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3
Q

EXPERIMENTAL METHOD
Contrast the different conditions of the IV

A

control condition: experience no manipulation
experimental condition: experience manipulation

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4
Q

EXPERIMENTAL METHOD
Define operationalisation

A

clearly defining the variables to more easily measure them

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5
Q

EXPERIMENTAL METHOD
What is a hypothesis?
How many hypotheses do we need to write for an investigation? Outline these and any strands of them.
What are the golden rules for writing hypotheses?

A

hypothesis: a prediction we have before tje experiment on the outcome of the study

we always write 2 hypotheses:
null: predicts no difference
alternative
alternative: predicts a difference/relationship
–> directional (one-tailed): we likely know the outcome (generally follows previous research)
–> non-directional (two-tailed): we don’t know what the outcome is likely to be

golden rules:
- “There will be…”
- include the operationalised IV and DV

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6
Q

RESEARCH ISSUES
Contrast extraneous variables with confounding variables using the example of the effects of video games on aggression. What are the different types of extraneous variables?

A

extraneous variables (EV): unwanted variables that could affect the DV
–> participant variables: individual differences
–> situational variables: any feature of the experiment

confounding variables (CV): type of EV which varies systematically with the IV

IV = video games, DV = aggression
EVs: sleep, hunger, upbringing/home life, stress, drug/alcohol use, circumstances, pre-existing anger issues
CVs: type of video game (violent or not), previous exposure/experience

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7
Q

RESEARCH ISSUES
Outline 2 ways we can reduce the effects of EVs and CVs, with examples

A

randomisation: use of change methods to reduce researcher’s unconscious biases when designing an experiment/investigation
e.g.) randomly allocating ptps to control or experimental groups/randomising the order that ptps complete conditions

standardisation: where all the ptps are subject to the same environment, info and experience
e.g.) giving same instructions to all ptps

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8
Q

RESEARCH ISSUES
Contrast demand characteristics with investigator effects, using examples

A

demand characteristics: cues revealing the aim of the study to the ptp, causing them to alter their behaviour
e.g.) questions asked, setting/location of experiment, researcher smiling at ptp in encouragement, ptp already heard about the study etc

investigator effects: unwanted influence of the investigator, giving away the aim of the study accidentally - subconscious or conscious influence
e.g.) conditions/groups obviously separated, odd/obvious instructions, different conditions for different groups

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9
Q

ETHICAL GUIDELINES
Name and outline the 5 ethical guidelines

A
  • informed consent: ptps should be made aware of the aims procedure, their rights and how their data will be used
  • deception: researcher should avoid deliberately misleading ptps at any stage of the experiment
  • confidentiality: ptps have the right to control info about themselves (privacy) and the right to have any personal data protected
  • right to withdraw: ptps should be able to stop the research at any time and request that the researcher withdraws their data
  • protection from harm: ptps should not be placed at any more risk than they would experience in their daily lives - includes physical and psychological harm
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10
Q

ETHICAL GUIDELINES
Outline how to deal with each ethical guideline is it is broken. (i.e. ways to get around each one)

A
  • informed consent: ptps should sign a consent form/we may seek additonal ways to get consent
  • deception & right to withdraw: ptps should be given a full debrief, made aware of researcher’s true aims and any other details they were not supplied with; this will also include the right to withdraw
  • confidentiality: personal details must be protected; researchers normally refer to ptps as numbers or initials; it’s stadard practise to remind ptps that their data will be kepy anonymous before and after the research
  • protection from harm: ptps should be given a full debrief; they should be reassured that their behaviour was typical; in extreme cases, counseilling should be offered
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11
Q

ETHICAL GUIDELINES
Besides a consent form from the ptp before the research, what 3 methods can we use to get consent?

A
  • presumptive consent: similar group of people to ptps is asked for consent, then ptp is assumed to also consent
  • prior general consent: ptps give consent to take part in a number of different studies, including one that will involve deception; so ptps are effectively consenting to beibg deceived
  • retrospective consent: ptps are asked for consent during debrifing after the research
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12
Q

ETHICAL GUIDELINES
Explain what is meant by a cost-benefit analysis.

A

weighing up the costs of the research (breaking ethical guidleines) and the benefits (what good can come of the research) - f the benefits ourwigh the costs then the research should go ahead

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13
Q

SAMPLING
Define participant, sample and target population.

A
  • ptp = a person taking part in the experiment
  • sample = the group of ptps
  • target population = all the people a psychologist wants to study
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14
Q

SAMPLING
Name and outline the 5 sampling methods.

A
  • random - every member of the target population has an equal chance of being selected
  • systematic - every nth persn is chosen from a list
  • stratified - the proportion of people in population subgroups (strata/layers) are refleted in the sample
  • opportunity - whoever is available at the time of the sampling will be inclluded
  • volunteer - ptps ‘self-select’
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15
Q

SAMPLING
Give one strength and one limitation of each sampling method.

A

RANDOM
+ potentially unbiased
- difficult and time-consuming to conduct (gathering a complete list of target population can be difficult)

SYSTEMATIC
+ objective
- time-consuming

STRATIFIED
+ reflective of taregt population
- the strata cannot reflect individual differences so a complete representation is not possible

OPPORTUNITY
+ convenient, cheaper
- researcher bias and not representative of target population

VOLUNTEER
+ easy, minimal input from researcher
- volunteer bias (may attract a certain ‘profile’ of people who want to impress the researcher => demand characteristics)

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16
Q

PILOT STUDIES
Outline what is meant by a pilot study. Why might researchers do this?

A

pilot study: a small-scale trial run of an investigation, used to identify any potential issues and to modify the design or procedure, saving time in the long run
- smaller sample
- ‘road checks’ the procedure to ensure it runs smoothly
- practise using the chosen self-report methods to remove or reword ambiguous or confusing questions
- in observational studies: useful to check coding systems

17
Q

VALIDITY
Define internal validity. How can psychologists ensure high internal validity in their research?

A

internal validity: the extent to which we are measuring what we set out to measure.

ensuring high internal validity:
- standardised procedures
- careful control of extraneous variables
- clear operationalisation of IVs and DVs

18
Q

VALIDITY
Differentiate a single-blind and a double-blind procedure.

A

single-blind: only the experimenter is aware of the conditions of the experiment
–> vulnerable to investigator effects by accidentally giving away hints
double-blind: neither experimenter nor ptp is aware of the conditions of the test being conducted.

19
Q

VALIDITY
Define external validity and its 3 types.

A

external validity: the extent to which our findings are generalisable to different times, people and places.

population validity: the extent to which our findings are generalisable to the target population
ecological validity: the extent to which our findings are generalisable to a natural setting (as opposed to a lab)
temporal validity: the extent to which our findings are generalisable to modern day/into the future; this concerns the ‘shelf-life’ of the research

20
Q

EXPERIMENTAL DESIGN
Define experimental design and the 3 types.

A

experimental design: the way participants are allocated to different conditions of the IV

types:
- independent groups: ptps only take part in one condition of the experiment
- repeated measures: ptps take part in both conditions of the experiment
- matched pairs: ptps are matched in terms of key variables such as IQ, gender and age. one is in control group and the other is in experimental group

21
Q

EXPERIMENTAL DESIGN
Outline one strength and two weakness of a repeated measures design.

22
Q

EXPERIMENTAL DESIGN
Outline three strengths and one weakness of a repeated measures design.

23
Q

EXPERIMENTAL DESIGN
Outline one strength and one weakness of a repeated measures design.