Experimental Research
Experimental research, often considered to be the “gold standard” in research designs,
is one of the most rigorous of all research designs. In this design, one or more independent
variables are manipulated by the researcher (as treatments), subjects are randomly assigned to
different treatment levels (random assignment), and the results of the treatments on outcomes
(dependent variables) are observed. The unique strength of experimental research is its
internal validity (causality) due to its ability to link cause and effect through treatment
manipulation, while controlling for the spurious effect of extraneous variable.
Experimental research is best suited for explanatory research (rather than for
descriptive or exploratory research), where the goal of the study is to examine cause-effect
relationships. It also works well for research that involves a relatively limited and well-defined
set of independent variables that can either be manipulated or controlled. Experimental
research can be conducted in laboratory or field settings. Laboratory experiments, conducted
in laboratory (artificial) settings, tend to be high in internal validity, but this comes at the cost
of low external validity (generalizability), because the artificial (laboratory) setting in which
the study is conducted may not reflect the real world. Field experiments, conducted in field
settings such as in a real organization, and high in both internal and external validity. But such
experiments are relatively rare, because of the difficulties associated with manipulating
treatments and controlling for extraneous effects in a field setting.
Experimental research can be grouped into two broad categories: true experimental
designs and quasi-experimental designs. Both designs require treatment manipulation, but
while true experiments also require random assignment, quasi-experiments do not.
Sometimes, we also refer to non-experimental research, which is not really a research design,
but an all-inclusive term that includes all types of research that do not employ treatment
manipulation or random assignment, such as survey research, observational research, and
correlational studies.
Basic Concepts
Treatment and control groups. In experimental research, some subjects are
administered one or more experimental stimulus called a treatment (the treatment group)
while other subjects are not given such a stimulus (the control group). The treatment may be
considered successful if subjects in the treatment group rate more favorably on outcome
variables than control group subjects. Multiple levels of experimental stimulus may be
administered, in which case, there may be more than one treatment group. For example, in
84 | S o c i a l S c i e n c e R e s e a r c h
order to test the effects of a new drug intended to treat a certain medical condition like
dementia, if a sample of dementia patients is randomly divided into three groups, with the first
group receiving a high dosage of the drug, the second group receiving a low dosage, and the
third group receives a placebo such as a sugar pill (control group), then the first two groups are
experimental groups and the third group is a control group. After administering the drug for a
period of time, if the condition of the experimental group subjects improved significantly more
than the control group subjects, we can say that the drug is effective. We can also compare the
conditions of the high and low dosage experimental groups to determine if the high dose is
more effective than the low dose.
Treatment manipulation. Treatments are the unique feature of experimental research
that sets this design apart from all other research methods. Treatment manipulation helps
control for the “cause” in cause-effect relationships. Naturally, the validity of experimental
research depends on how well the treatment was manipulated. Treatment manipulation must
be checked using pretests and pilot tests prior to the experimental study. Any measurements
conducted before the treatment is administered are called pretest measures, while those
conducted after the treatment are posttest measures.
Random selection and assignment. Random selection is the process of randomly
drawing a sample from a population or a sampling frame. This approach is typically employed
in survey research, and assures that each unit in the population has a positive chance of being
selected into the sample. Random assignment is however a process of randomly assigning
subjects to experimental or control groups. This is a standard practice in true experimental
research to ensure that treatment groups are similar (equivalent) to each other and to the
control group, prior to treatment administration. Random selection is related to sampling, and
is therefore, more closely related to the external validity (generalizability) of findings.
However, random assignment is related to design, and is therefore most related to internal
validity. It is possible to have both random selection and random assignment in well-designed
experimental research, but quasi-experimental research involves neither random selection nor
random assignment.
Threats to internal validity. Although experimental designs are considered more
rigorous than other research methods in terms of the internal validity of their inferences (by
virtue of their ability to control causes through treatment manipulation), they are not immune
to internal validity threats. Some of these threats to internal validity are described below,
within the context of a study of the impact of a special remedial math tutoring program for
improving the math abilities of high school students.
History threat is the possibility that the observed effects (dependent variables) are
caused by extraneous or historical events rather than by the experimental treatment.
For instance, students’ post-remedial math score improvement may have been caused
by their preparation for a math exam at their school, rather than the remedial math
program.
Maturation threat refers to the possibility that observed effects are caused by natural
maturation of subjects (e.g., a general improvement in their intellectual ability to
understand complex concepts) rather than the experimental treatment.
Testing threat is a threat in pre-post designs where subjects’ posttest responses are
conditioned by their pretest responses. For instance, if students remember their
answers from the pretest evaluation, they may tend to repeat them in the posttest exam.
Not conducting a pretest can help avoid this threat.
E x p e r i m e n t a l R e s e a r c h | 85
Instrumentation threat, which also occurs in pre-post designs, refers to the possibility
that the difference between pretest and posttest scores is not due to the remedial math
program, but due to changes in the administered test, such as the posttest having a
higher or lower degree of difficulty than the pretest.
Mortality threat refers to the possibility that subjects may be dropping out of the study
at differential rates between the treatment and control groups due to a systematic
reason, such that the dropouts were mostly students who scored low on the pretest. If
the low-performing students drop out, the results of the posttest will be artificially
inflated by the preponderance of high-performing students.
Regression threat, also called a regression to the mean, refers to the statistical tendency
of a group’s overall performance on a measure during a posttest to regress toward the
mean of that measure rather than in the anticipated direction. For instance, if subjects
scored high on a pretest, they will have a tendency to score lower on the posttest (closer
to the mean) because their high scores (away from the mean) during the pretest was
possibly a statistical aberration. This problem tends to be more prevalent in nonrandom
samples and when the two measures are imperfectly correlated.
Two-Group Experimental Designs
The simplest true experimental designs are two group designs involving one treatment
group and one control group, and are ideally suited for testing the effects of a single
independent variable that can be manipulated as a treatment. The two basic two-group designs
are the pretest-posttest control group design and the posttest-only control group design, while
variations may include covariance designs. These designs are often depicted using a
standardized design notation, where R represents random assignment of subjects to groups, X
represents the treatment administered to the treatment group, and O represents pretest or
posttest observations of the dependent variable (with different subscripts to distinguish
between pretest and posttest observations of treatment and control groups).
Pretest-posttest control group design. In this design, subjects are randomly assigned
to treatment and control groups, subjected to an initial (pretest) measurement of the
dependent variables of interest, the treatment group is administered a treatment (representing
the independent variable of interest), and the dependent variables measured again (posttest).
The notation of this design is shown in Figure 10.1.
Figure 10.1. Pretest-posttest control group design
The effect E of the experimental treatment in the pretest posttest design is measured as
the difference in the posttest and pretest scores between the treatment and control groups:
E = (O2 – O1) – (O4 – O3)
Statistical analysis of this design involves a simple analysis of variance (ANOVA)
between the treatment and control groups. The pretest posttest design handles several threats
to internal validity, such as maturation, testing, and regression, since these threats can be
expected to influence both treatment and control groups in a similar (random) manner.
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Sunday, 13 March 2016
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