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Quasiexperiment lack control group or pretest observation

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Identification and study of plausible threats to internal validity. ... control studies include: birth control pills, smoke and cancer, etc.. Case ... – PowerPoint PPT presentation

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Title: Quasiexperiment lack control group or pretest observation


1
Quasi-experiment lack control group or pretest
observation
  • Ilham El-saleh Alma Rangel

2
Definition
  • Quasi-experimental designs are commonly employed
    in the evaluation of educational programs when
    random assignment is not possible or practical.
    However, these designs are subjected to many
    limitations and interpretations that we are going
    to see in different examples.

3
Why do researchers using such designs? The best
design for a given study
  • Practical necessities imposed by funding, ethics,
    or administrators.
  • Logistical constraints that occur when an
    intervention has already been fielded before the
    evaluation of the intervention is designed.

4
Principles address requirements in such design
  • Identification and study of plausible threats to
    internal validity.
  • Primacy of control by design.
  • Coherent pattern matching.

5
What does Control or equivalent group design
mean?
  • The presence of control group in a design will
    give the researcher the chance to compare
    between the result of two different groups. Each
    of two groups received two different kinds of
    treatment. For example, one group of students
    might receive math instruction using a whole new
    program while the other receives a different math
    program (nothing). After certain time, a test can
    be administered to see which program was more
    effective.

6
Threats to Validity
  • There are several factors that can jeopardize the
    validity of an experimental design
  • They can be broken into internal and external
    validity
  • Internal Validity. (interpretability) Are our
    claims concerning the effects of the treatment
    valid in this particular experiment?
  • External Validity. (generalizability) Can our
    results from this experiment be generalized to
    other populations and settings?

7
Internal Validity
  • Eight different classes of extraneous variables,
    which, if not controlled in the experimental
    design, might produce effects confounded with the
    effect of the experimental stimulus.
  • History - the specific events occurring between
    the first and second measurement in addition to
    the experimental value, creating rival hypotheses
    (O1 X O2)
  • Maturation - processes within the respondents
    operating as a function of the passage of time
    per se (not specific to the particular events),
    including growing older, hungrier, more tired,
    etc.
  • Testing - the effects of taking a first test upon
    the scores of a second testing.
  • Instrumentation - changes in the calibration of a
    measuring instrument or changes in the observers
    or scorers used, may produce changes in the
    obtained measurements.

8
Internal Validity
  • Statistical Regression - operating where groups
    have been selected on the basis of their extreme
    scores, i.e., tendency toward the mean.
  • Selection - biases resulting in differential
    selection of respondents for the comparison
    groups (X O1, O2)
  • Experimental Mortality - differential loss of
    respondents from the comparison groups.
  • Selection-Maturation Interaction, etc. - any of
    the extraneous variables can have a combined
    effect that can be mistaken for the effect of the
    experimental variable.

9
Designs without control groups( non-treatment
control group)
  • One group posttest only
  • X O1
  • Improving onegroup posttest with multiple
    posttest
  • X O1A O1B. O 1N

treatment
posttest
treatment
10
More..
  • One group pretest posttest
  • O1 X O2

pretest
treatment
posttest
11
Example One Group Pre-test Post-test Design
  • O1 X O2
  • X learn SPSS
  • O1 time to solve problems in another
  • language (e.g. SAS)
  • O2 time to solve problems in SPSS
  • Does not control for history, maturation, etc.

12
Pretest-Posttest Design
13
More
  • Improving the one group pretest posttest using
    double pretest
  • O1
    O2 X O3

treatment
posttest
pretest
pretest
14
More
  • One group pretest posttest using a non
    equivalent dependent variable. (same group at
    times 1 2)
  • O1A , O1B X O2A
    , O2B

pretest
pretest
treatment
posttest
posttest
15
More
  • The removed- treatment design
  • O1 X O2
    O3 X O4
  • (The outcome rises and falls with the presence of
    the treatment)
  • The repeated- treatment design
  • O1 X O2 X
    O3 X O4

pretest
treatment
posttest
pretest
posttest
No treatment
treatment
remove
pretest
posttest
Re treatment
posttest
pretest
16
Designs that use control group but no pretest
  • Add a control group that receives no treatment,
    with the control group selected to be as similar
    as possible to the treatment group.
  • In this design there is not a pretest measure on
    the outcome variable.

17
Notation Symbols
  • O Observation
  • X Treatment
  • R Random Assignment to Group
  • -- or NR No Random Assignment

18
Quasi-Experimental Designs that use Control
Groups but No Pretest
  • Posttest-Only Design With Nonequivalent Groups.
  • NR X O1
  • --------------------------------------
  • NR O2
  • Posttest-Only Design using an Independent Pretest
    Sample.
  • NR O1 X O2
  • --------------------------------------
  • NR O1 O2
  • Posttest-Only Design using Proxy Pretests.
  • NR OA1 X OB2
  • ----------------------------------------
  • NR OA1 OB2

Dashed line between groups means that they were
not randomly formed
19
Proxy-Pretest Design
  • In this design one gathers the pretest
    information after the experimental treatment has
    started. In other words, one finds find a proxy
    variable that would estimate pretest performance.
  • For example, suppose I ask the following
    question Does completion of EDCI 627 have an
    effect on a students knowledge of statistics?
    Ideally I would measure the students statistical
    knowledge at the beginning of the semester, but
    suppose that the question did not occur to me
    until the middle of the semester. I might decide
    to use as a proxy-pretest students performance
    in their EDCI 627 (statistics) class. My control
    group might consist of a group of students taking
    some other class (not 627).

20
Cont. Proxy-Pretest Design
  • For each student I would obtain a continuous
    measurement of the students performance in EDCI
    627 and, at the end of the semester, a continuous
    measurement of the students knowledge of
    statistics.
  • The proxy pretest design is not one you should
    ever select by choice. But, if you find yourself
    in a situation where you have to evaluate a
    program that has already begun, it may be the
    best you can do and would almost certainly be
    better than relying only on a posttest-only
    design.

21
The Posttest-Only Design Using Matching or
Stratifying
  • Matching. The units in the Treatment and Control
    groups are exactly equal (rather than just
    similar) on a matching variable.
  • Stratifying. The units are placed into
    homogeneous sets that contain more units than the
    experiment has conditions.
  • Methods for Matching. Exact matching requires
    units to have exactly the same score within a
    match. However, some units will not have an exact
    match if samples are small, if the distribution
    of participants between groups on the matching
    variable is uneven, or if variables are measured
    using very fine gradations.

22
Problems with matching..
  • There is always the possibility of selection
    bias.
  • Matching in quasi-experimentation works least
    effectively when it is done on an unstable or
    unreliable variable and when the nonequivalent
    groups from which the matched sets are drawn are
    increasingly dissimilar when matched
  • Two methods that can help to counteract these
    problems are
  • - Select groups that are similar as possible
    before matching, as much as the context and
    research question allow.
  • - Use matching variables that are stable and
    reliable.

23
Other Quasi-Experimental Designs..
  • The Posttest-Only Design Using Internal Controls.
  • - Internal control group are plausibly drawn
    from a population similar to that from which the
    treatment units are taken. Internal controls do
    not guarantee similarity.
  • The Posttest-Only Design Using Multiple Controls
    Groups.
  • - The use of multiple nonequivalent control
    group.
  • The Posttest-Only Design Using Predicted
    Interaction.
  • - The objective is predict statistical
    interaction. It can be useful for predict a
    complex data pattern, outcomes measures can be
    reliably measured, etc..

24
Improving Designs without Control groups by
Constructing Contrasts other than with
independent control groups.
  • When it is not possible to gather prospective
    data on the kinds of independent control groups,
    it is sometimes possible to construct contrast
    that try to mimic the function of an independent
    control group. Three such contrasts are
  • - Regression Extrapolation Contrasts. It
    compares actual and projected posttest scores.
  • - Normed Comparison Contrasts. It compares
    treatment recipients to normed sampled.
  • - Secondary source Contrasts. It compares
    treatment recipients to samples drawn form
    previously gathered data, such as
    population-based surveys.

25
The Case Control Design
  • In this design, one group consists of cases that
    have the outcome of interest, and the other group
    consists of controls that do not have it.
  • - Ex. If we compare the exposure
    distribution between the groups of subjects with
    and without disease.
  • The outcome in this design is typically
    dichotomous.
  • Cases and controls are then compared using
    retrospective data to see if cases experienced
    the hypothesized cause more often than controls.
  • The case-control design is excellent for
    generating hypotheses about causal connections.
    Some case-control studies include birth control
    pills, smoke and cancer, etc.. Case-control
    studies are more feasible than experiments in
    cases in which an outcome is rare or takes years
    to develop they are often cheaper and
    logistically easier to conduct and they may
    decrease risk to participants who could be
    needlessly exposed to a harmful experimental
    treatment.

26
Sources
  • http//www.socialresearchmethods.net/kb-old/quasio
    th.htm
  • http//faculty.ncwc.edu/toconnor/308/308lect06.htm
  • http//core.ecu.edu/psyc/wuenschk/docs2210/Researc
    h-8-QuasiExpDesign.doc
  • Campbell, Shadish Cook, 2002. Experimental and
    Quasi-Experimental Designs for Generalized Causal
    Inference. Houghton Mifflin Company
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