Final Exam MC questions Flashcards

1
Q

We can have a multiple baseline design across three entities. Which is NOT one of those entities:
a. Participants
b. Settings
c. Behaviors
d. Conditions

A

D. Conditions

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2
Q

When we establish two or more steady baselines and apply the intervention to one participant, setting, or behavior at a time, we are using which design?
a. ABAB
b. Alternating treatments
c. Multiple baseline
d. Changing criterion

A

C. Multiple Baselines

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3
Q

We guess where the first baseline data path would keep going, and then determine if there is a distance between the predicted and actual data in the intervention phase. Which level of visual analysis in a multiple baseline design is this?
a. Prediction
b. Replication
c. Verification

A

A. Prediction

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4
Q

We guess where the second baseline data path would keep going, and then determine if there is a distance between the predicted and actual data in the intervention phase. Which level of visual analysis in a multiple baseline design is this?
a. Prediction
b. Replication
c. Verification

A

C. Verification

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5
Q

In a multiple baseline design, when baseline data in the 2nd and 3rd tiers stay at baseline levels even when intervention is applied in earlier tiers, and change only when the intervention is applied at that tier, we call this:
a. Prediction
b. Replication
c. Verification

A
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6
Q

Which of the following statements about multiple baseline designs is NOT true:
a. Extend the “verification window” for increased experimental control
b. Start intervention after the most stable baseline first
c. If experimental control is lost, conduct more experimentation
d. Ensure at least five replications before evaluating verification

A
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7
Q

Which is the most common number of tiers in multiple baseline designs
a. 2
b. 5
c. 3-5
d. More than 5

A

C. 3 -5

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8
Q

Which is true about the multiple baseline across participants design?
a. It is strong and common
b. It is weak and common
c. It is strong and uncommon
d. It is weak and uncommon

A

B. It is weak and common

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9
Q

When baseline data are not collected every session, this is most likely a:
a. Reversal design
b. Multiple baseline design
c. Multiple probe design
d. Changing criterion design

A

C. Multiple probe design

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10
Q

In a multiple baseline across settings design, if we get generalization across settings, we ___ experimental control
a. Have
b. Lost

A

B. Lost

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11
Q

Which of the following is NOT a reason for using a multiple probe design?
a. There is zero responding in baseline
b. There is a high chance of reactivity (presence of observer influencing behavior)
c. The measurement requires too much time
d. The previously published studies used that design

A

D. The previously published studies used that design

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12
Q

The most important time to include baseline data in a multiple probe design is:
a. In the first session
b. After an effect was observed at a higher tier
c. After a vacation

A

B. After an effect was observed at a higher tier

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13
Q

Which of the following is NOT true of a “probe”?
a. It is an intermittent data point
b. It includes assessment but not teaching
c. It includes assessment and teaching

A

C. It includes assessment and teaching

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14
Q

When baselines in Tiers 2 and beyond begin at later points than Baseline in Tier 1, this is called:
a. Multiple baseline design
b. Multiple probe design
c. Nonconcurrent multiple baseline design
d. Delayed multiple baseline design

A

D. Delayed Multiple Baseline Design

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15
Q

If baseline does not span before and after the introduction of the independent variable in the previous tier,
a. You have replication, but not verification
b. You have replication and verification
c. You have no replication or verification

A
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16
Q

Which is a stronger design?
a. Multiple baseline design
b. Delayed multiple baseline design

A

A. Multiple Baseline Design

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17
Q

When three AB designs evaluating the same dependent variable and independent variable are conducted sequentially in time and have different lengths of baseline, and then stacked on top of each other, this is best referred to as:
a. Multiple baseline design
b. Delayed multiple baseline design
c. Nonconcurrent multiple baseline design
d. Multiple probe design

A

C. Nonconcurrent Multiple Baseline Design

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18
Q

Which of the following is NOT true of the nonconcurrent multiple baseline design?
a. Appropriate when a concurrent MB design is not feasible
b. Controls for maturation, but not for history effects
c. Allows prediction and replication, but not verification
d. Is stronger than a concurrent multiple baseline design

A

D. Is stronger than a concurrent MB design

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19
Q

True or false: A multiple baseline design is good for demonstrating the effects of an intervention, but not for an in-depth analysis of that intervention
a. True
b. False

A

A. True

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20
Q

An initial baseline is followed by a series of treatment phases consisting of successive levels of behavior required for reinforcement. This is a description of which design?
a. ABAB
b. Alternating treatments
c. Multiple baseline
d. Changing criterion

A

D. Changing Criterion

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21
Q

In a changing criterion design, experimental control is demonstrated when:
a. The level of responding matches each new criterion
b. There is prediction, verification, and replication
c. There is a distance between the data paths
d. When there is a change in the dependent variable when, and only when, the independent variable is applied

A

A. the level of responding matches each new criterion

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22
Q

True or false: For increased experimental control, it is good to vary the lengths of phases.
a. True
b. False

A

A. True

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23
Q

In a changing criterion design, if there is low variability, can have ___ criterion changes.
a. Small
b. Large

A

B. Large

24
Q

In a changing criterion design, after many successful phase changes, returning to a previous criterion level is a way to achieve
a. Prediction
b. Replication
c. Verification

A
25
Q

The changing criterion design is most useful for interventions that involve
a. Systematic desensitization
b. Communication training
c. Problem behavior reduction
d. Feeding protocols

A

A. Systematic Desensitization

26
Q

True or false: In a changing criterion design, you can evaluate the training of a new skill
a. True
b. False

A

B. False

27
Q

If reinforcement is contingent on a behavior that is different than the previous two behaviors, this is which schedule of reinforcement?
a. Lag 2
b. VR 2
c. FR 2
d. VI 2

A

A. Lag 2

28
Q

Which dimension of ABA means we have to tie our practices back to the basic principles of behavior?
a. Analytic
b. Technological
c. Conceptually systematic
d. Parsimony

A

C. Conceptually Systematic

29
Q

The first step in determining experimental control in an ABAB (Reversal) design is:
a. Prediction: draw a line extending the first baseline data, determine if there is a distance between the predicted an actual data in the first intervention phase
b. Verification: determine if the data in the second baseline phase return to (or towards) the level in the first baseline phase
c. Replication: draw a line extending the second baseline data, determine if there is a distance between the predicted an actual data in the second intervention phase

A

A. Prediction `

30
Q

The third step in determining experimental control in an ABAB (Reversal) design is:
a. Prediction: draw a line extending the first baseline data, determine if there is a distance between the predicted an actual data in the first intervention phase
b. Verification: determine if the data in the second baseline phase return to (or towards) the level in the first baseline phase
c. Replication: draw a line extending the second baseline data, determine if there is a distance between the predicted an actual data in the second intervention phase

A

C. Replication

31
Q

In an ABAB design, if there is prediction but no verification, you:
a. Are done with the analysis: there is experimental control
b. Are done with the analysis: there is no experimental control
c. Determine if there is replication to make conclusions about experimental control

A

b. Are done with the analysis: there is no experimental control

32
Q

We base decisions about prediction, verification, and replication on:
a. Level
b. Level and trend
c. Level, trend, and variability

A

c. Level, trend, and variability

33
Q

True or false: When determining verification, the second baseline data need to return to the exact same levels as the first baseline data
a. True
b. False

A

B. False

34
Q

A researcher ____ make small adjustments to the independent variable during a study
a. Can
b. Cannot

A

A. Can

35
Q

With dangerous behavior, it is a good idea to implement a second baseline for ___ sessions.
a. Many
b. Few

A

B. Few

36
Q

When looking at a graph quickly and the data seem to overlap between baseline and intervention, it is a good idea to:
a. Conclude no experimental control
b. Examine the data closely for prediction, verification, and replication

A

B. Examine the data closely for prediction, verification, and replication

37
Q

When a researcher wants to evaluate an intervention that is already in place, which design is appropriate:
a. AB
b. ABAB
c. BAB

A

C. BAB

38
Q

Which of the following is the strongest design?
a. AB
b. ABAB
c. BAB

A

B. ABAB

39
Q

When researchers discover that planned conditions do not control behavior, they may introduce new conditions. Which condition sequence is most representative of this:
a. ABAB
b. BAB
c. ABACABAC
d. AB

A

c. ABACABAC

40
Q

A potential limitation of evaluating multiple treatments is “sequence effects.” The best way to rule out control by condition sequence is to:
a. Implement the same condition for two phases in a row
b. Change the order of conditions with each new participant
c. Evaluate the treatments and then implement baseline sessions
d. Evaluate no more than four treatments in one study

A

b. Change the order of conditions with each new participant

41
Q

Which of the following is NOT a limitation of the reversal design:
a. Unethical to remove effective interventions
b. Some behaviors do not return to baseline levels when the intervention is removed
c. It is difficult to compare interventions
d. Can have prediction and verification but not replication

A
42
Q

The rapid alternation of two or more independent variables while measuring a dependent variable is a description of which experimental design?
a. ABAB
b. Alternating treatments
c. Multiple baseline
d. Reversal

A

b. Alternating treatments

43
Q

How do we know if there is experimental control in an alternating treatments design graph?
a. Using prediction, verification, and replication
b. There is a substantial distance between the data paths
c. There is a substantial distance between the predicted and actual data paths
d. There is a change in the dependent variable when, and only when, the independent variable is applied

A

b. There is a substantial distance between the data paths

44
Q

Functional analyses are most often analyzed using which experimental design?
a. Reversal
b. Alternating treatments
c. Multiple baseline
d. AB

A

B. Alternating Treatments

45
Q

True or false: In an alternating treatments design, we can conclude experimental control if there is some overlap in the data
a. True
b. False

A

A. True

46
Q

When determining experimental control in an alternating treatments design graph, distance between the data paths is most important:
a. On the left side of the graph
b. In the middle of the graph
c. On the right side of the graph

A

C. On the right side

47
Q

Which best depicts a correct example of the order of conditions A and B in an alternating treatments design:
a. ABABABABAB
b. AAAAABBBBB
c. ABABAABABB
d. BBBBBAAAAA

A

a. ABABABABAB

48
Q

True or false: A no-treatment control condition is required in an alternating treatments design
a. True
b. False

A

b. false

49
Q

True or false: A baseline is required in an alternating treatments design
a. True
b. False

A

b. false

50
Q

Sometimes, researchers add a final phase to an alternating treatments design with the:
a. Best treatment
b. Worst treatment
c. Control condition

A

A. Best Treatment

51
Q

One treatment influencing the effects of another treatment in an alternating treatments design is referred to as:
a. History effects
b. Sequence effects
c. Multiple treatment interference
d. Multiple baseline interference

A

C. Multiple treatment interference

52
Q

One treatment influencing the effects of another treatment in an alternating treatments design can be ruled out by:
a. Comparing only two treatments
b. Including an extended baseline phase
c. Including a no-treatment control condition
d. Isolating the more effective treatment in a final phase

A

d. Isolating the more effective treatment in a final phase

53
Q

The extent to which the researcher implemented the intervention according to how it was written is called:
a. Treatment integrity
b. Interobserver agreement
c. Reliability
d. Social validity

A

a. Treatment integrity

54
Q

Which of the following is NOT a reason to collect treatment integrity data:
a. To ensure changes in behavior are due to the written protocol
b. To increase confidence in concluding a functional relation
c. To ensure clinicians implement treatments accurately
d. To ensure data collection procedures are implemented consistently

A

b. To increase confidence in concluding a functional relation

55
Q

Research has shown that the _____ the integrity with implementing a treatment procedure, the ______ the learning of the participants.
a. higher, worse
b. lower, worse

A

b. lower, worse

56
Q
A