Student Learning Outcomes
At the completion of this unit of instruction students will be able to:
Introduction
Q. In experimental research what are we primarily interested in establishing?
A. Cause and effect. Remember however, that statistics alone
don't do this. Need to examine all aspects of the experimental
arrangements to determine alternative explanations.
Q. What might be possible alternative explanations?
A. Incorrect statistics, poor control of variables, inappropriate
subjects, incorrect interpretation of results, etc. Also - we
have concerns about the experimental design which affects
the internal and external validity of experiments (Q. What are
these two types of validity?)
Q. In striving for high internal and external validity we are forced to compromise. Why?
A. The more we control the variables in an experiment the less
we are able to generalize outside of this setting. It's a dilemma
and source of disagreement in some areas where researchers seem
to be obsessed with one or other orientation.
These threats to IV and EV were closely examined more than
30 years ago by Campbell and Stanley and resulted in a long research
article that was later published as a small book (show?)
and has become the bible of design for researchers.
Eight Threats to Internal Validity
So let's look at the threats C&S identified. There were
eight identified threats to IV:
History - events occurring other than part of the experiment (including weather, season, etc.)
Maturation - passage of time
Testing*- repeat effects of testing, e.g. usually people do better on second attempt at any test because of familiarity, etc.
Instrumentation*- calibration, differences between observers
Statistical regression - danger if groups are selected on extreme scores
Selection biases - if groups are not random and start different
Experimental mortality*- loss of subjects due to non random reasons
Selection x maturation interaction - affects nonequivalent
(non random) groups where the passage of time might affect one
more than the other.
Rosenthal added a ninth threat which he entitled expectancy
- when researchers have a bias toward some type of result
and are in a position to influence findings. This occurs when
the researchers have the opportunity to record data based on their
subjective impressions.
You should know these nine threats to IV. I use mnemonic MIS
RM SMITHE. (Show how this helps by drawing on board.)
These factors affect IV - which is what?
Q. How do you think we might control many of these threats to IV?
A. By random assignment of subjects to the experimental
groups. In fact only three of the threats remain if random assignment
occurs (see asterisks). In other words randomization does not
control for these factors influencing both groups evenly.
Q. Placebos, blind and double blind arrangements are also ways to minimize threats to IV. What are they?
A. Placebos are used to see if any changes are real or due
to other reasons. In blind experiments the subject does not know
if he or she is in the control or experimental groups. In double
blind neither the subject not the researcher know the subject's
group. These techniques help to control expectancy effects.
External Validity
What about EV? C&S identified 4 additional factors that
could influence our ability to generalize:
Reactive or interactive effects of testing - a pretest
often sensitizes a person in a direction that in effect changes
the person. For example, if you are told you have high cholesterol
level, or shown the tar in cigarettes and the blackened sick looking
lung tissue
Interaction of selection biases and experimental treatment
- sometimes treatments are only effective with certain subjects.
For example, you use students in your conditioning class to test
your ideas on swim training, or swimmers to test your ideas on
conditioning. In either case to what population is it reasonable
to generalize your findings? (Maw study for injured runners used
regular students as subjects)
Reactive effects of experimental arrangements - it is
often difficult to generalize from lab settings. (Hawthorn effect?
Subjects performance changes when attention is paid to them.)
Multiple treatment interference - it is difficult to
generalize if subjects are exposed to more than one level of treatment.
For example, if you use the same subjects to evaluate the effect
of different training programs there will inevitably some carryover.
Q. What is the key to minimizing threats to EV? (Think about it - what is your concern and how can you increase your ability to generalize?)
A. By random selection. Solomon 4 group design allows
examination of the effects of testing. Multiple treatment effects
can be controlled by matching.
Types of Experimental Designs
Attempting to control many of these threats involves thinking
about your experimental design. Lots of different designs but
text divides them into three categories
1. preexperimental
2. experimental
3. quasi experimental
Q. Can you distinguish?
A.
1. preexperimental - little control and no random assignt.
2. experimental - random assignt.
3. quasi experimental - non random groups but attempts made
to control threats.
1. One shot study - difficult to conclude anything - can't really attribute the performance to the treatment.
2. One group pretest-post test - can now see improvement but you don't know why (could be maturation, testing, history etc.)
3. Static group comparison - problem is that the groups are not equivalent at the beginning so hard to conclude the reason for any observed differences.
4. Randomized groups design - is like #3 but with random groups. Controls for many of the threats to IV
5. Pretest - post test randomized group design - Useful if interested in the amount of change as a result of treatment. Possible reactive effects of testing is a threat to IV but should be evened out between groups. However reactive effects of testing remain a threat to EV.
6. Solomon four group design - can now evaluate the effects of testing in EV. But you need lots of subjects!
7. Time series designs - can compare rates of changes over time, e.g. between O1 - O4 and O5 - O7 as well as differences between O4 - O5.
8. Reversal design - similar to above, allows insertion of treatment then withdrawal, then treatment.
9. Non-equivalent control groups - we attempt to find similar groups and use as controls. Is similar to design #5 but without the randomization.
10. Ex Post Facto design - Is like #3 but with no control
over the treatment the groups received. For example, we could
go back and look at records of students in several school districts
and perform a statistical analysis.
Other Types of Quasi-Designs
The three additional types described in this section illustrate that experimental design is not static but changes as the result of applying innovative and creative thought to research questions. For example, we will be having class presentations on single subject designs when we discuss case studies. These designs have already been used in many research studies conducted in sport psychology.
Knowledge Check
Think about a possible problem in your area of interest that
could be examined using an experimental design. Using the notations
(R, O, T etc.) contained in the text draw out the design. Be sure
you can explain it.
(Revised 2/3/99)