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what’s the difference between between-subject design, between-group design and independent-measures experimental design?
nothing, it’s the same thing

explain what’s a between-subject design
different group of participants is assigned to each condition
each group receives a different experimental treatment (IV) and they are all compared

what’s the key element of between-subject design?
we use separate groups of participants for different conditions
we then compare the data (DV) to across groups to look for differences

the treatment is the [DV/IV] and the data is the [DV/IV]
treatment = IV (what we control)
data = DV (what we measure)
why is between-subjects design an independent measure?
because participants only experience one level of the IV, meaning that there is only one score per participant
true or false: all IVs can be measured in both between-subject or within-subject designs
false: some IVs can, but other can be measure only with a between-subjects design
ex (between only): age, gender
ex (within or between): teaching method, video condition
why do we prefer between-subject designs for kids?
they have limited attention span
between-subjects allows one condition per infant, which is perfect for their attention
ex: having one kid go through one condition (between-sub) VS having one kid go through three conditions (within-sub)
define “systematic variance”
difference in the DV between groups (between the means of different treatment groups)
define “non-systematic variance”
scores varying within groups
individual difference occurring by chance
what’s the difference between systematic and non-systematic variance?
systematic: difference of the scores/DV between groups
non-systematic: difference of the scores/DV within groups, individual differences occurring by chance
define “non-systematic variance”
scores that vary within the group, individual differences that occurred by chance
[systematic/non-systematic] variance is an important source of error that must be minimized
non-systematic: it’s the one that varies within-group, individual differences that occur by chance
what’s another name for “treatment index”
F-ratio
define “experimental error”
chance factors that cause differences across any condition and that cannot be controlled
*works for between or within
true or false: you can completely eliminate experimental error
false: it’s non-systematic variance, there will always be some difference
if we treated the groups in a between-subject designs the exact same way, would you obtain the same scores? explain why
no: there will always be some experimental error that will cause some differences between the mean
what are the components/causes of systematic/between-subjects variance? (2)
treatment effect
experimental error: factors that cannot be controlled and will cause differences across conditions
→ systematic variance = treatment effects + experimental error
[systematic/non-systematic] variance is any differences between subjects who are treated alike
non-systematic, within-group: everyone goes through the same conditions
[systematic/non-systematic] variance = experimental error
non-systematic
treatment index/F-ratio = x ÷ y or (z+a) ÷ b
F-ratio:
between-groups variance (systematic) ÷ within-group (non-systematic) variance
(treatment effects + experimental error) ÷ experimental error
true or false: the F-ratio is not sensitive to the absence/presence of treatment effect (effect of the IV)
false: it is
if your F-ratio is large, you [can/cannot] reject your null hypothesis. if your F-ratio is low, you [can/cannot] reject your null hypothesis
large = reject H0: Fstat > Fcrit
small = retain H0: Fstat < Fcrit
large between-groups/systematic variance is [good/bad], large within-group/non-systematic variance is [good/bad] because […]
large systematic: good
large non-systematic: bad
explanation
reminder: F-ratio = systematic ÷ non-systematic
when you have a large denominator (within-subjects variance), you will get a small number
you want a large F-ratio in order to see the effect of your IV and reject the H0
how can you avoid getting small F-ratios? (2)
have large a numerator
have a small denominator
*reminder: F-ratio = systematic ÷ non-systematic variance
if the between-groups/systematic variance > within-group/non-systematic variance, then the F-ratio is [near 0 and small/positive and large]
if the between-groups/systematic variance < within-group/non-systematic variance, then the F-ratio is [near 0 and small/positive and large]
between > within, F-ratio = positive and large (good)
between < within, F-ratio = near 0 and small (not so good)

what does the circled bar represent?
it’s the standard error: value of the variance within each condition
high bar = a lot of non-systematic variance (no good)
small bar = not a lot of non-systematic variance (good)
define “single-factor analysis of variance” (ANOVA)
test to determine if there are statistically significant difference between the means of three (or more) independent groups
there is one independent variable with three conditions
ex: compare driving performance (IV) with cellphone, handfree phone or no phone (conditions)
why would you use a single-factor analysis of variance (ANOVA) instead of doing multiple tests? (ex: phone vs handfree, handfree vs none, phone vs none)
an ANOVA will provide you with stronger evidence for cause-and-effect relationship than a two-group design
how can you maximize between-group differences?
by comparing two distinct things (distinct enough so that you can notice some differences)
how can you minimize within-group differences? (3)
standardize experiment procedure so that all participants are treated the same way
minimize individual differences:
hold extraneous variable constant or restrict the range
use a large sample size
what are the major sources of confounding variables in a between-groups design? (2)
individual differences/assignment bias: process of assigning participants to different conditions produces groups with different characteristics
ex: age, sex, IQ, socioeconomic status
environmental variables: uncontrolled characteristics in the environment that may differ across groups
ex: room, lighting, time of day, noise
define “assignment bias”
process of assigning participants in conditions produces group with different characteristics
why is assignment bias a threat to internal validity?
because it offers an alternative explanation to the changes seen in the DV: is it because of the IV or because of how we assigned our participants?
how can you avoid experimental bias or individual differences?
by controlling or keeping fixed individual difference variables in each condition (ex: have an age range)
define “environmental variables”
uncontrolled characteristics in the environment that may differ across your groups
true or false: environmental variables are only extraneous variables
false: if they differ between groups, they go from extraneous to confound as they will also affect the DV
how can you establish equivalent groups of participants? (3)
create them equally
treat them equally
compose them of equivalent individuals
define “randomization”
participants are randomly assigned to groups to ensure that groups are as equal as possible before treatment
why is randomization the most powerful technique to control the effects of pre-existing differences?
because it equalizes/spreads the difference across all conditions
what’s the difference between random sampling and randomization?
random sampling: random selection from the population that will constitute your sample
randomization: random assignment into groups after the random sampling
define “free random assignment”
ensuring that participants are assigned to groups only based on chance (everyone has an equal chance of being assigned to one of the conditions)
true or false: free random assignment is guaranteed to lead to equality/non-systematic variance
false: not sure if you’ll end up with perfect equality because it’s at random
why is free random assignment used even if it won’t lead to perfect equality between the groups?
the groups won’t be perfectly matched, but the difference is negligible
the important differences that we will see between the groups will be caused by treatment
true or false: free random assignment also works on small samples
false
define “matching”
match participants on pre-existing differences that may be related to differences in the DV so that they are equivalent on critical variables)

what are the steps of matching? (4)
identify the variable(s) to be matched
measure and rank subjects on the variable for which control is desired
segregate subjects into matched pairs on that variable
randomly assign pair-members to the conditions
true or false: you can also match in groups and not on individuals only
true:
ex: high > 110, medium = 90-110, low < 90

define “attrition”
participants leaving the study before it’s finished
when does attrition become a problem? (2)
when participants in one group leave more than participants in other groups as the groups are no longer equivalent (differential attrition)
*if equal participants from each group leave equally, then it’s not a problem
threat to internal validity: is the difference between groups is due to treatment or differential attrition
what’s the difference between attrition and differential attrition?
attrition: participants leaving the study before it’s completed
differential attrition: participants from one group leave more than participants from other groups
what are the communication between groups that can threaten internal validity? (3)
diffusion/spreading: treatment effects from one condition spread to another condition
true effects of treatment may be masked by shared information
resentful demoralization: perceived inequality that influence behaviour
define “resentful demoralization”
perceived inequality that can affect behaviour (ex: knowing that other condition receives money but not you)
what are the advantages of between-subjects design? (4)
simple design: each score is independent from other scores
clean and uncontaminated by other treatment factors (no carryover effects, practice effects)
experiment takes less time for each participant
causality can be established
why are between-subjects preferred over within-subject?
within-subject has carryover effects as the same participant goes through many conditions
the design will have many types of carryover effects (first, second, nth order) that will increase with the amount of condition going through
carryover effects create more bias as the number of conditions increase
ex: smaller effect from A to B than from A to C
which means that it’s biased: your response changes because of the experience they got from previous conditions and not by the treatments
you don’t need to worry about this with between-subjects!
what are the disadvantages of between-subjects designs? (4)
requires many participants as one participant contributes to one score only
can be difficult to recruit enough participants in special populations
individual differences and environmental differences can exist: groups must be equivalent before manipulation
generalization (external validity) can be hard if you’re always holding constant the extraneous variable
what are the solutions to counter assignment bias, experimenter expectancy bias and subject-expectancy bias? (4)
participants are blind/don’t know the condition they are in
experimenters are blind/don’t know the condition the participants are in
both the participants and the experimenters are blind
data analyst is blind (instead of saying treatment, placebo, we say 1, 2)
when should you use or not use a between-subjects deisgn?
should: avoid carryover or comparison effects
should not: when you want similar anchoring across conditions (ex: asking someone how high is the Olympic stadium and asking someone else how high is a tree… how high compared to what?)
define “comparison effects”
within-subjects designs raise participants’ perception of difference across conditions
what should you try to avoid when doing a between-subjects design? (4*)
carryover effects
participant awareness
changes in measurement properties/response over time
*ecological validity (you want ecological validity, participants are usually not exposed to all levels of a variable)