Answers to
Study Questions
for
Chapter 10
(Don’t forget that the companion website also has multiple choice
questions that you can take for practice. You will find them here: http://www.southalabama.edu/coe/bset/johnson/dr_johnson/2mcq.htm)
10.1. What is a quasi-experimental design, and when do you use such a design?
Quasi-experimental research designs are
experimental designs that do not provide for full control of extraneous
variables primarily because of the lack of random assignment to groups. They
are stronger than the three “weak” designs discussed in the last chapter, but
they are not as strong as the five “strong” designs that we discussed in the
last chapter.
·
You
could say that they are kind of “in between” designs; they are not great, but
they are not too bad either. Because they are classified as a type of
experimental research, the independent variable must manipulated (although real
world events that are highly similar to
experimenter manipulation also may be appropriate for quasi-experimental
research).
/------------------------------------/------------------------------------/
Weak Quasi Strong
Designs Designs Designs
10.2. What requirements must be met to reach a
valid causal inference when using
a quasi-experimental design?
Basically, you must meet the
same three necessary conditions that we discussed in the last chapter. Here are
these extremely important conditions again presented in a Table from a later
chapter in your book. Again, whenever you are trying to establish a cause and
effect relationship as being present you must, at a minimum, do these three
things:

You must memorize these
three conditions and use them whenever you are thinking about cause and effect
in research.
·
Quasi-experimental
research is strong on conditions one and two.
·
Therefore,
condition three is where you will have to do the most thinking and planning
when you design a quasi-experimental research study.
10.3. What is a nonequivalent
comparison-group design and what are the essential features of this design?
O1
X1 O2
-------------------------
O1
X2 O2
where
O1 and O1 are the pretests
X1 and X2 are the levels of the
independent variable
and O2 and O2 are the posttests.
Here are the essential
features of this design:
·
Manipulation
of the independent variable
·
Pretest
for all of the comparison groups
·
Posttest
for all of the comparison groups
·
No
random assignment to the comparison groups (which as you can imagine is going
to cause some problems with this design as compared to the strong “randomized”
experimental designs.
10.4. How are rival explanations addressed when using the nonequivalent
comparison-group design?
First, when designing a
study that will be based on this design, you must try to identify groups that
are as similar as possible on any factors that may affect the dependent
variable. Next, ask yourself this question: “Looking at these groups, do I have
any reason to expect them to be different in any way?” If yes, ask what are
those characteristics? and how can you control for them? The logic here is that
you don’t want the groups to differ on any extraneous variables that may affect
the dependent variable. You want the groups to be as similar as possible on all
factors except the independent variable. That is, you want the only
systematic difference between the groups to be the systematic variation of the
independent variable.
The biggest threat to the
internal validity of these designs is selection (i.e., the groups might
be composed of different kinds of people with different characteristics such as
group differences in age, gender, IQ, reading ability, etc.). Other threats are
mortality and the selection interactions such as the
selection-maturation effect, and the selection-history effect.
You need to try to control
for all extraneous variables on which the groups may differ using control
techniques such as statistical control (e.g., analysis of covariance)
and matching.
10.5. What types of biases can exist when using the nonequivalent
comparison-group
design?
Here is a list of the most
common types of biases that can exist in the nonequivalent-comparison group
design. They are all potentially important and must be addressed by a
researcher. In my opinion (Burke Johnson) the omnipresent and most serious
problem is selection bias (what we called earlier differential selection); this
is always a problem in this design because you do not have random assignment to
the groups, and therefore the groups may differ on some extraneous variables
and not just differ on the levels of the independent variable that they get. In
other words, you must always be concerned about differences in the makeup of
the comparison groups.

10.6. What is the best way of determining whether a threat is plausible
when using
the nonequivalent comparison-group design?
1.
First,
you should examine the way in which the participants were assigned to the
groups and try to determine what variables the groups may differ on.
·
If
you identify any extraneous variables that the groups differ on and which are
probably also related to the dependent variable then you should consider these
to be plausibly alternative explanations, unless they are addressed and
controlled by the researcher.
2.
Second,
you should look for pretest differences because big pretest differences will
tend to lead to big posttest differences regardless of any posttest differences
caused by the independent variable.
·
If
the researcher did not use any technique to control for pretest differences,
then this should be considered to be a plausible alternative explanation (i.e.,
a threat).
3.
Third,
all of the other potential biases shown above in Table 10.1 must be considered.
·
If
any seems likely to be present and nothing was done to minimize its impact,
then you should consider it to be a plausible threat to the study.
The bottom line is this: Was
the threat identified by the researcher?, and did the researcher use any of the
control techniques (e.g., statistical control such as analysis of covariance
and matching) to minimize the problem?
·
If
the answer is NO, then any threat identified by you as being plausible is a
problem and the researcher will need to explain why he or she did not attempt
to address the problem during the planning and conduct of the study and what
this means for the study results.
10.7. What are the essential design characteristics
of an interrupted time-series design?
The interrupted time-series
design is shown in the following figure from your textbook:

As you can see above, the
three major design components are
·
multiple
pretests (it does not have to be exactly five as shown in the picture)
·
a
treatment (i.e., an intervention to be studied)
·
multiple
posttests (it does not have to be exactly five as shown in the picture)
Note that the type of
treatment can be one that occurs specifically between the time points 5 and 6,
but the type of intervention can also be one that is “turned on” after
time point 5 and continues throughout the posttesting period (i.e.,
throughout points 6 to 10).
10.8. How is a treatment effect demonstrated when
using an interrupted time-series
design?
It is demonstrated by
comparing the pretest pattern (its height, slope, and shape) with the posttest
pattern. Note that the pretest pattern shows the baseline (i.e., the pattern
before any intervention).
Here is an example of a
clear pattern of results, suggesting that the treatment has an impact on the
dependent variable:

10.9. How are potential confounding variables ruled out when using the
interrupted
time-series design?
The key strategy of this
design is to have enough pretests and posttests to determine the pattern of
results on the dependent variable (i.e., on the variable that you are trying to
influence). By including multiple pretests and posttests you are able to
avoid many of the problems present in the weak design called the one-group
pretest-posttest design that was discussed in the last chapter. The one-group
pretest-posttest design has only one pretest and one posttest.
If you look at the following
figure, you will see that the one-group pretest-posttest design would give
misleading results in cases A, B, and C, but the interrupted time-series design
provides the data in all of the cases that enables you to make an accurate
determination of the impact (or lack of impact) of the treatment or
intervention.

·
Visual inspection is sometimes used to make a determination of impact; however, if there
is much variation in the data, statistical analysis is usually needed in
order to provide high statistical conclusion validity.
·
Note
that the primary threat to the validity in an interrupted time-series design
is the history effect; that is, if some additional factor occurs after the
baseline period along with the treatment then this represents a rival
explanation (for example, if you were studying the impact of a change in the
speed limit on traffic fatalities you would not want to select localities where
a new drunk driving law was implemented at the same time as the speed limit
change).
10.10. What are the essential characteristics of the
A-B-A design?
Here is a picture of the
A-B-A design:

The A-B-A design is a
single-case experimental design in which the response to the experimental
treatment condition (B) is compared to baseline responses (A) taken before and
after administering the treatment condition.
·
The
treatment effect in this design is determined by comparing the pattern of
baseline behavior with the pattern of treatment behavior.
·
You
would look for a discontinuity in the baseline and treatment patterns, such as
differences in the slope and/or level of responses on the dependent variable.
·
For
example, if the treatment is supposed to cause an increase a certain behavior
then an impact would be shown by a low (A), high (B), low (A) set of responses.
·
If
the treatment is supposed to cause a decrease a certain behavior then an impact
would be shown by a high (A), low (B), high (A) set of responses.
10.11. How does the A-B-A design rule out rival
hypotheses and demonstrate the effect of
an experimental treatment condition?
If you used an A-B design
rather than an A-B-A design, history would be a threat (i.e., anything
that co-occurred with the treatment). However, if you use the A-B-A design then
history is likely to be ruled out through what is called reversal.
Reversal occurs when the behavior to reverts back to baseline when the
treatment is removed. It is unlikely
that some extraneous history event or variable would start exactly the same
time as the treatment, occur during the treatment, and then precisely disappear
when the treatment is removed. That’s why reversal is so useful.
·
Short
treatment periods help to facilitate reversal in some situations.
10.12. What are the primary problems that can exist
when using the A-B-A design, and
how can they be solved?
The primary limitation with
the A-B-A design is that some behaviors will not revert back to the
original baseline level when the treatment is removed, making rival hypotheses
such as history more plausible.
·
To
solve this problem you need to use a different design, in particular, the
multiple-baseline design.
A second limitation is that
the experiment ends with the baseline condition, and this means that the
experiment does not end by providing the benefits of the treatment.
·
This
limitation is overcome by using an A-B-A-B design rather than an A-B-A design.
10.13. How does the multiple-baseline design
demonstrate a treatment effect?
·
First,
note that in the multiple-baseline design, the treatment condition is
successively administered to different participants (or to the same participant
in several settings) after baseline behaviors have been recorded for different
periods of time. In other words, the treatment has a delayed or staggered
onset for the different participants.
·
Notice
that the effectiveness of this design does not hinge on a reversal of behavior
(as was the case in the A-B-A and A-B-A-B designs).
·
The
“fingerprint” or pattern of results that suggests an effect would be a change
in behavior (in the predicted direction) after each onset of the treatment.
·
For
example, the following pattern of results supported the researchers’ theory
(i.e., the reading rates would increase when they implemented their assisted
reading treatment for each of three participants).

·
Notice
how the onset of the treatment was staggered (i.e., occurs at different times)
for the different participants in the above research study and notice the
pattern of results.
10.14. What is the primary problem that can be
encountered in using the
multiple-baseline design?
A limitation is that some
behaviors, people, or settings may be interdependent; that is, when you change
one person, behavior, or setting another person, behavior, or setting being
measured in the study may also be affected. When this happens you don’t get the
pattern of responses needed to draw a firm conclusion about the effectiveness
of the treatment (because in this design changes in the measure should clearly
occur with each onset of the treatment condition).
10.15. When would you use the changing-criterion
design?
The changing-criterion
design is used when the researcher wants to demonstrate that the participant’s
behavior can be altered by changing the criterion for success during successive
treatment periods. For example, a researcher might want to “shape” a
participant’s behavior or the researcher might want to increase the accuracy, frequency,
or amount of a behavior over time.
10.16. What are the essential characteristics of the
changing-criterion design?
The characteristics are
shown in the following figure from your textbook:

This type of design includes
a baseline phase and several treatment phases where the criterion of required
performance is successively increased or decreased.
·
(Take
a look at Figure 10.16 to see a pattern of results that supported the
researcher’s hypothesis.)
Here is one more study
question that was not included in your book, but I want to add...
10.17 Identify and discuss the
four methodological issues that must be considered when using a single-case
research design.
The four issues are baseline
(e.g., When has a stable baseline been reached? How much variability or
fluctuation is present? Is there a trend present? What is the direction of the
trend?), changing one variable at a
time (Make sure you only change one variable at a time so that no
confounding of causes will be present), length of phases (How long
should a phase be? Generally, all phases should be the same length), and assessment
of treatment effect (How do you decide if the treatment caused a change in
the dependent variable? Visual inspection and statistical analysis are used for
this).