Seth M' Noar, Ph'D' - PowerPoint PPT Presentation

1 / 20
About This Presentation
Title:

Seth M' Noar, Ph'D'

Description:

Allows one to examine effects of the IV manipulation (treatment) above and ... Note: One is essentially treating the pretest as an additional IV. Group 4. Group 2 ... – PowerPoint PPT presentation

Number of Views:28
Avg rating:3.0/5.0
Slides: 21
Provided by: sethmich
Category:
Tags: noar | note | one | seth

less

Transcript and Presenter's Notes

Title: Seth M' Noar, Ph'D'


1
Experiments
  • Seth M. Noar, Ph.D.
  • CJT665
  • Department of Communication
  • University of Kentucky

2
2 Broad Types of Research
  • Surveys Observations that occur in natural
    settings
  • Often operate in real world settings
  • But, causality is difficult to demonstrate
  • Experiments Studies in which data are collected
    under conditions where 1 or more variables are
    manipulated
  • Often operate in an artificial setting
  • But, causality is easier to demonstrate

3
2 Broad Types of Research (contd)
  • These two types are complementary in many ways
    ideal program of research takes advantage of both
  • Research design similar to statistics should
    choose the best and most appropriate research
    design
  • However, resources and other factors may help to
    dictate what design is feasible
  • Large randomized trials cost a lot of money
  • Some perfect experiments are unethical to
    conduct

4
Experiments
  • True experiment involves
  • IV manipulated variable
  • DV variable expected to be influenced by the
    manipulation of the IV
  • Pool of participants who are randomly assignment
    to groups (e.g., control and experimental)
  • Note Random assignment distinguishes
    experimental from quasi-experimental designs

5
Experimental Designs
  • 5 Types of Designs
  • Pretest-Posttest Control Group Design
  • Posttest Only Control Group Design
  • Solomon Four Group Design
  • Factorial Designs
  • Blocking Designs
  • There are also many variations on these designs

6
Pretests
  • Pretest advantages
  • Demonstrate that randomization worked that
    groups are equivalent at baseline
  • If groups are different in some way, can
    statistically control for this since we have
    pretest data
  • Gives one data to include/exclude individuals
    from experiment, and use in other ways
  • However, are their some cases where having no
    pretest is better?

7
(No Transcript)
8
(No Transcript)
9
Pretests (contd)
  • Disadvantages
  • Can clue participants as to the purpose of the
    study
  • Can sensitize individuals to the IV
  • Opens up more potential threats to internal
    validity

10
Solomon 4 Group Design
  • Combines the previous 2 designs together
  • Can evaluate several effects within 1 experiment
  • Allows one to examine effects of the IV
    manipulation (treatment)
  • Allows one to see if the pretest had an effect
  • Allows one to examine effects of the IV
    manipulation (treatment) above and beyond any
    pretest effects (interaction)
  • Note One is essentially treating the pretest as
    an additional IV

11
(No Transcript)
12
Solomon as 2 x 2 Factorial
Pretest
No Pretest
Treatment
Treatment Main Effect
No Treatment
Pretest Main Effect
13
Factorial Designs
  • Factorial Designs involve more than 1 IV
  • For example, a 2 X 2 design
  • Sensation Value Low, High
  • Need for cognition Low, High
  • What analysis tool does one use for a factorial?

14
2 x 2 Factorial
High NFC
Low NFC
High SV
Low SV
15
Blocked / Mixed Designs
  • Blocked or mixed designs are appropriate when we
    have factors we are interested in that we cannot
    manipulate
  • Examples IQ, Gender, Race
  • Key feature is this participants are sorted into
    categories (blocked) according to some variable
    and then are assigned to groups

16
(No Transcript)
17
Validity
  • 2 major types of validity in experiments
  • Internal validity extent to which one can make
    causal inferences about the IV-DV relationship
  • External validity The extent to which one can
    generalize findings of the study to the
    population and to other contexts
  • These are generally mutually exclusive, and have
    mutually exclusive threats

18
Threats to External Validity
  • Key issue here is generalizability extent to
    which findings can be expected to be replicated
    with other samples, at other times and places,
    and under other conditions
  • Thus, non-random sampling, interactions between
    IVs and the context in which they are delivered,
    and other factors can affect external validity
  • Often we do NOT have true random samples
  • Best we can do is attempt to replicate our
    findings in many samples as they become available

19
Threats to Internal Validity
  • History An event takes place between pre and
    post test (MM example)
  • Maturation Individuals mature in some way
    between pre and post test (Anti-marijuana
    example)
  • Testing Scores on post test change because of
    exposure to pretest
  • Instrumentation Scores on post test change
    because of unreliable measurement (not actual
    change). (This happens more with subjective
    measures).
  • Statistical Regression Unreliability or
    measurement error results in scores away from the
    mean at time 1, and then back to the mean at time
    2

20
Threats to Internal Validity (contd)
  • 6. Selection If posttest scores differ
    across groups, this may be due to selection
    factors that went into creating the groups
    (gender diffs w/ college students)
  • 7. Experimental Mortality Differences that
    occur in the posttest that are due to
    differential attrition across groups
  • 8. Selection Interactions If selection
    factors went into creating the groups, these
    specially selected groups may encounter
    differential history, maturation, testing, or
    other effects.
  • Note These threats, when they occur, make it
    very difficult to tell if it was in fact the IV
    that lead to changes in the DV
Write a Comment
User Comments (0)
About PowerShow.com