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9. Quantitative Research Designs. Learning Objectives. Identify Criteria For Exploratory, Descriptive, And Explanatory Studies Define Experimental Research Differentiate Between Internal And External Validity In Experimental Designs Identify Six Threats To Internal Validity
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9 Quantitative Research Designs
Learning Objectives • Identify Criteria For Exploratory, Descriptive, And Explanatory Studies • Define Experimental Research • Differentiate Between Internal And External Validity In Experimental Designs • Identify Six Threats To Internal Validity • Identify Three Threats To External Validity
Learning Objectives Distinguish Among True Experimental, Quasi-Experimental, And Pre-Experimental Designs Describe Three True Experimental Designs Describe Two Quasi-experimental Designs Describe Two Pre-experimental Designs
Learning Objectives Discuss Four Types Of Nonexperimental Research Designs Recognize Two Types Of Settings In Which Research Is Conducted Identify Factors That Influence The Choice Of Research Designs Critique The Design Section Of Quantitative Studies
Learning Objective OneIdentify Criteria For Exploratory, Descriptive, And Explanatory Studies
Exploratory Studies • Little known about phenomenon • Flexible data collection approach • Qualitative and quantitative • Hypotheses not appropriate
Descriptive Studies • Phenomena described • Relationship between variables examined • More information about variable(s) • Test hypotheses
Explanatory Studies • Explanations for relationships among phenomena • Rigorous • Experimental research • Control over research conditions • Manipulate one or more variables
Experimental Research • Cause + effect • Manipulate and control independent variable • Measure dependent variable
Problems With Experimental Research • Casual relationships difficult to establish • Avoid using word prove • Controls difficult to apply to human beings
Learning Objective ThreeDifferentiate Between Internal And External Validity In Experimental Designs
Internal Validity • Degree to which changes in effect can be attributed to cause • Threats • Other factors that influence dependent variable • Constitute rival explanations or competing hypotheses
External Validity • Degree to which results can be generalized • Questions to ask • With what degree of confidence can findings be transferred to the entire population? • Will these findings hold true with other groups and in other times and places?
Relationship Between Internal and External Validity • As control for internal increases, external decreases • As concern for external increases, internal may be affected • Need to find balance
Learning Objective FourIdentify Six Threats To Internal Validity
Six Threats to Internal Validity • Selection bias • History • Maturation • Testing • Instrumentation change • Mortality
Selection Bias • Results due to subject differences • Not due to independent variable manipulation • Means to control • Random group assignment
History • Event other than the experimental treatment occurs during the course of study. • Event influences dependent variable. • Means to control • Simultaneous control and comparison groups • Random assignment of subjects to groups
Maturation • Changes occur within subjects during study. • Changes influence the study results. • Means to control • Simultaneous control and comparison groups
Testing • Influence of pretest or baseline data knowledge on posttest score
Instrumentation Change • Difference between pretest and posttest measurement • Caused by change in accuracy rather than experimental treatment • Means to control • Judge training sessions • Trial instrument runs to check for changes • Continue to check instrument accuracy
Mortality • Subject does not complete study. • Attrition rate different between groups • Means to control • No research design to control • Establish strong researcher-participant relationship
Learning Objective FiveIdentify Three Threats To External Validity
Major Threats to External Validity • Hawthorne effect • Experimenter effect • Reactive effects of the pretest
Hawthorne Effect • Participants’ responses influenced by knowing they are being observed • Means to control • Double-blind experiment
Experimenter Effect • Experimental research • Researcher characteristics or behaviors influence subject behaviors. • Examples of influential characteristics • Facial expression • Clothing • Age • Gender • Body build
Rosenthal Effect • Nonexperimental research • Interviewer characteristics or behaviors influence respondent’s answers.
Reactive Effects of the Pretest • Subjects sensitized to experimental treatment because of pretest • Examples of pretests • Paper-and-pencil test • Knowledge of baseline data
Difference Between Internal and External Pretest Threats • Internal threat: pretest or baseline data knowledge cause of posttest results • External threat: pretest or baseline data knowledge catalyst (indirect cause)
Learning Objective SixDistinguish Among True Experimental, Quasi-Experimental, AndPre-Experimental Designs
Experimental Research Designs • True experimental • Quasi-experimental • Pre-experimental
True Experimental Design • Great deal of control • Internal validity threats minimized • Causality inferred with confidence
True Experimental Design Criteria • Researcher manipulates the experimental variable(s). • One experimental group and one comparison group • Subjects randomly assigned to groups
Quasi-Experimental Design • No comparison group • Subjects not randomly assigned to groups
Advantages and Disadvantages of Quasi-Experimental Design • Advantages • Real world more closely approximated • Disadvantages • Not as much control as true experimental design
Pre-Experimental Design • Considered weak • Researcher has little control.
Learning Objective SevenDescribe Three True Experimental Designs
Experimental Designs • Pretest-posttest control group design • Posttest-only design • Solomon four-group design
The Pretest-PosttestControl Group Design • Most frequently used experimental design • Criteria • Subjects randomly assigned to groups • Pretest given to both groups • Experimental group receives experimental treatment. • Comparison group receives routine treatment or no treatment. • Posttest given to both groups
The Pretest-PosttestControl Group Design (cont’d) • Advantages • Controls for all internal validity threats • Controls for initial differences by adjusting posttest scores statistically • Disadvantages • External threat of reactive effects of the pretest • Can only be generalized to situations in which pretest is administered
The Posttest-OnlyControl Group Design • Subjects randomly assigned to groups • Experimental group receives the experimental treatment. • Comparison group receives routine treatment or no treatment. • Posttest given to both groups
Advantages of Posttest-Only Control Group Design • Easier to carry out • Eliminates reactive effects of the pretest on the posttest
The Solomon Four-Group Design • All subjects are randomly assigned to one of four groups. • Two groups—experimental group 1 and comparison group 1— pretested • Two groups—experimental group 1 and experimental group 2—receive experimental treatment. • Two groups—comparison group 1 and comparison group 2—receive routine treatment or no treatment.
Solomon Four-Group Design • Posttest given to all four groups • Advantages • Minimizes threats to both internal and external validity • Differences between groups can be associated with the experimental treatment. • Disadvantages • Requires a large sample • Statistical analysis is complicated.
Learning Objective EightDescribe Two Quasi-Experimental Designs
Quasi-Experimental Designs • Nonequivalent control group design • Time-series design
The NonequivalentControl Group Design • Similar to pretest-posttest control group design • No random assignment of subjects to groups
Internal Validity in Nonequivalent Control Group Design • Threats to internal validity controlled • History • Testing • Maturation • Instrumentation change • Threats to internal validity that remain • Selection bias
Time-Series Design • Periodic observations or measurements of subjects • Experimental treatment administered between two of the observations