Lecture 18: Single-Subject Designs Flashcards

1
Q

how do we statistically analyze between-subjects designs?

A

an independent subjects t-test or between-subjects ANOVA

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2
Q

how do we statistically analyze within-subjects designs?

A

a dependent subjects t-test or repeated measures ANOVA

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3
Q

Single-subject (single-case) designs

A

research designs that use the results from a single participant or subject

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4
Q

goal of single-subject designs

A

Establish the existence of cause-and-effect relationships

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5
Q

how are single-case experimental designs conducted

A

by manipulating an IV and controlling extraneous variables to prevent alternative explanations for the research results

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6
Q

alternative explanations for research results in a single-subject design

A
  • Baseline
  • Repeated observations
  • Replication
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7
Q

evaluating results from a single-case study

A
  • Data are evaluated in a simple graph because statistical tests for significance cannot be used
  • Contrary to what is stated in the textbook, several statistical significance tests could be used to compare the level and trend between the A and B phases
  • However, such a graph by itself is not enough to show that the treatment caused a behavioural change
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8
Q

why are graphs not enough to show that the treament caused a behavioural change?

A
  • No control over extraneous variables
  • This could be the result of chance
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9
Q

phase

A

series of observations of the same individual under the same conditions

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10
Q

when are baseline observations made?

A

when no treatment is being administered

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11
Q

baseline phase

A

a series of baseline observations

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12
Q

baseline notation

A

Identified by the letter A

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13
Q

treatment observations

A

observations made when a treatment is being administered

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14
Q

treatment phase

A

a series of treatment observations

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15
Q

treatment notation

A
  • Identified by the letter B
  • Subsequent treatments are identified by subsequent letters (ex. c, d, e)
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16
Q

function of baseline and treatment annotation

A

Allows researchers to describe the phases in a study by using a sequence of letters

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17
Q

consistent level

A
  • A series of measurements that are all nearly the same magnitude
  • Graphed data points cluster around a horizontal line
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18
Q

consistent trend

A
  • Differences from one measurement to the next that are consistently in the same direction and nearly the same magnitude
  • Graphed data points cluster around a sloping line
19
Q

stability

A
  • The degree to which the observations show a pattern of consistent level or consistent trend
  • Stable data may show minor variations from a perfectly consistent pattern
  • Variations should be relatively small and the linear pattern relatively clear
20
Q

strategies for dealing with unstable data

A
  • Wait until the data stabilize
  • Average a set of two or more observations
  • Look for patterns within the inconsistency
21
Q

length of a phase

A
  • To establish a pattern (level or trend) within a phase and to determine the stability of the data within a phase, a phase must consist of a minimum of three observations
  • Two observations, by themselves, do not provide enough information to determine a pattern.
  • Additional observations beyond the first two are essential to establish level, trend, and stability.
  • Typically, five or six observations are necessary to determine a clear pattern
  • When high variability exists in the data points, additional observations should be made
22
Q

phase change

A

a manipulation of the independent variable

23
Q

what are accomplished with phase changes?

A
  • Implementing a new treatment
  • Withdrawing a treatment
  • Changing a treatment
24
Q

function of changing phases

A

Initiates a new phase in which the researcher collects observations under new conditions

25
Q

when should we change phases?

A

When a clear pattern has emerged from the preceding phase

26
Q

what factors should we consider when assessing participants’ responses to phases?

A
  • If they are improving without treatment, don’t implement the treatment.
  • If they are deteriorating quickly, implement the treatment right away.
  • If the treatment produces immediate and severe deterioration, cease or modify treatment immediately.
27
Q

visual inspection techniques

A

characteristics that help determine whether there is a meaningful change between phases

28
Q

examples of visual inspection techniques

A
  • Change in the average level
  • Immediate change in level
  • Change in trend
  • Latency of change
29
Q

tools to enhance visual inspection techniques

A
  • Use lines representing a level in each phase and a band representing +/- 2 standard deviations
  • Use lines representing the trend in each phase
30
Q

phases of an ABAB design

A

A baseline phase (A), followed by treatment (B), then a return to baseline (A), and finally a repetition of the treatment phase (B)

31
Q

goal of an ABAB design

A

to demonstrate that the treatment causes changes in the participant’s behaviour

32
Q

demonstrating that the ABAB design causes a change in behaviour

A
  • The pattern of behaviour in each treatment phase (different from the pattern in each baseline phase)
  • The changes in behaviour from baseline to treatment and from treatment to baseline (the same for each of the phase-change points in the experiment)
33
Q

limitations of the ABAB design

A
  • Withdrawal from treatment
  • This may not result in a change in behaviour (the patient is cured)
  • This may result in a slight change but not a return to the baseline
  • This may cause an ethical problem if the treatment is working for the participant
34
Q

variations on the ABAB design

A
  • Sometimes researchers add a treatment or modify the sequence of baseline and treatment phases.
  • Creates a complex design
  • Researchers must incorporate new treatments into the phase sequence to prove a causal relationship.
  • ABBCAC, ABCBC, etc.
35
Q

multiple baseline design

A
  • The treatment phase is initiated for one baseline
  • Baseline observations continue for the other
  • The treatment is initiated for the second baseline at a different time
36
Q

multiple-baseline across subjects

A

the initial baseline phases correspond to the same behaviour for two separate participants

37
Q

multiple-baseline across behaviours

A

the initial baseline phases correspond to two separate behaviours for the same participant

38
Q

multiple-baseline across situations

A

the initial baseline phases correspond to the same behaviour in two separate situations

39
Q

component analysis designs

A
  • Each phase adds or subtracts one component of a complex treatment
  • Determines how each component contributes to the overall treatment effectiveness
  • Component analysis with a reversal design
  • Component analysis with a multiple-baseline design
40
Q

rationale for multiple-baseline designs

A
  • The criteria for a successful multiple-baseline experiment are essentially identical to the criteria described earlier to define the success of an ABAB design
  • There is a clear and immediate change in the pattern of behaviour when the researcher switches from a baseline to a treatment phase
  • The design includes at least two demonstrations that behaviour changes when the treatment is introduced
  • This replication is necessary to establish a causal relationship between treatment and behaviour
41
Q

strength of a multiple-baseline design

A
  • No return to baseline needed
  • Good for long-lasting treatments
42
Q

weaknesses of a multiple-baseline design

A
  • It can be difficult to identify similar but independent behaviours
  • Results can be compromised by individual differences between participants or between behaviours
43
Q

strengths of single-case designs

A
  • Allows researchers to establish cause-and-effect relationships with one participant or subject
  • Flexibility: the researcher is free to modify the treatment or change to a new treatment if a participant or subject fails to respond to the treatment
  • No need to standardize treatment across groups—a single participant or subject is used
44
Q

weakenesses of single-case designs

A
  • Relationship among variables is for only one participant or subject
  • May threaten external validity (generalization)
  • Multiple, continuous observations are required
  • Absence of statistical controls
  • Reliance on graphs to display data
  • Treatment effects must be large and immediate to produce a convincing graph