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EVAL 6970: Experimental and Quasi- Experimental Designs Dr. Chris L. S. Coryn Dr. Anne Cullen Spring 2012.

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Presentation on theme: "EVAL 6970: Experimental and Quasi- Experimental Designs Dr. Chris L. S. Coryn Dr. Anne Cullen Spring 2012."— Presentation transcript:

1 EVAL 6970: Experimental and Quasi- Experimental Designs Dr. Chris L. S. Coryn Dr. Anne Cullen Spring 2012

2 Agenda Basic design elements and notation Quasi-experimental designs that either lack a control group or lack pretest observations on the outcome Midterm examination Case study

3 Questions to Consider What are the limitations of designs lacking either control groups and/or pretest observations? What simple strategies can be used to improve these types of designs? Why are such designs sometimes the only ones that can be used?

4 Basic Design Elements and Notation

5 Assignment Random assignment Cutoff-based assignment Other nonrandom assignment Matching and stratifying Masking

6 Measurement Posttest observations – Single posttests – Nonequivalent dependent variables – Multiple substantive posttests Pretest observations – Single pretest – Retrospective pretest – Proxy pretest – Repeated pretests over time – Pretests on independent samples Moderator variable with predicted interaction Measuring threats to validity

7 Comparison Groups Single nonequivalent groups Multiple nonequivalent groups Cohorts Internal versus external controls Constructed contrasts – Regression extrapolation contrasts – Normed contrasts – Secondary data contrasts

8 Treatments Switching replications Reversed treatments Removed treatments Repeated treatments

9 Notation X= treatment O= observation R= random assignment NR= nonrandom assignment X= removed treatment X + = treatment expected to produce an effect in one direction X - = conceptually opposite treatment expected to reverse an effect C= cutting score - - -= non-randomly formed groups … = cohort

10 Logic of Quasi-Experimentation

11 Rationale Quasi-experiments are often a necessity given practical and logistical constraints – Greater emphasis on construct or external validity rather than cause-effect associations (least common) – Funding, ethics, administration (somewhat common) – The intervention has already occurred (most common) Sometimes they are the best alternative, even if causal inferences are weaker than is possible with other designs Even so, great care must be taken when planning such studies as numerous threats that cannot be controlled are often operating

12 Central Principles Identification and study of plausible threats to internal validity – Careful scrutiny of plausible alternative explanations for treatment-outcome covariation Primacy of control by design – Use carefully planned and implemented design elements rather than statistical controls for anticipated confounds Coherent pattern matching – Complex (a priori) causal hypotheses that reduce the plausibility of alternative explanations

13 Designs without Control Groups

14 One-Group Posttest Only Design Absence of pretest makes it difficult to know if change has occurred and absence of a control group makes it difficult to know what would have happened without treatment XO1O1

15 One-Group Pretest-Posttest Design Adding a pretest provides weak information concerning what might have happened to participants had the treatment not occurred O1O1 XO2O2

16 One-Group Pretest-Posttest Design with Double Pretest Adding multiple pretests reduces the plausibility of maturation and regression effects Additional pretests can confirm maturational trends O1O1 O2O2 XO3O3

17 One-Group Pretest-Posttest Design Using a Nonequivalent Variable Measure A is expected to change because of treatment, B is not Both A and B are expected to respond to the same validity threats in the same way {O 1A, O 1B }X{O 2A, O 2B }

18 Lottery ticket sales in convenience stores after introduction of signs in store windows reading did you buy your ticket? A = sale of lottery tickets B = sale of alcohol C = sale of tobacco A A B B C C

19 Removed-Treatment Design Demonstrates that outcomes rise and fall with the presence or absence of treatment O1O1 XO2O2 O3O3 XO4O4

20 Generally interpretable outcome pattern O1O1 Outcome Worse Better O2O2 O3O3 O4O4 X X Uninterpretable outcome Interpretable outcome

21 Repeated-Treatment Design Few threats could explain a close relationship between treatment introductions and removals and parallel outcome changes O1O1 XO2O2 XO3O3 XO4O4

22 Mean narcotics use over multiple Methadone maintenance on/off conditions

23 A-B Designs Multiple-baseline design (a class of single- subject designs), or collection of A-B designs, to assess the effects of an intervention across separate baselines A = baseline B = treatment The intervention is introduced in a staggered manner and the baseline provides a predicted level of the dependent variable in absence of the treatment A-B-A designs are sometimes called removal designs (i.e., the treatment is removed)

24 Number of Accidents Weeks Baseline Treatment Site 1 Site 2 Site 3 Effect

25 Designs that use a Control Group but no Pretest

26 Posttest-Only Design with Nonequivalent Control Group Unknown pretest group differences make it extremely difficult to separate treatment effects from selection effects NRXO1O1 O1O1

27 Posttest-Only Design using an Independent Sample Pretest Assumes overlapping group membership Useful when pretest measurements may be reactive, cannot follow same groups over time, or when interested in studying intact communities whose members change over time NRO1O1 XO2O2 O1O1 O2O2

28 Posttest-Only Design using Proxy Pretest Proxy measures should be conceptually related to and correlated with outcome Can be used for a variety of purposes including indexing selection bias and/or attrition NROA1OA1 XOB2OB2 OA1OA1 OB2OB2

29 Case Control Studies Predominant method for many forms of epidemiological research Used to identify factors that may contribute to a condition by comparing subjects who have that condition (i.e., 'cases') with those who do not have the condition but are otherwise similar (i.e., 'controls') Famously, the association between smoking and lung cancer Similar in many respects to Scrivens GEM and MOM

30 Midterm Examination

31 The examination will consist of 50-75 multiple-choice items, scored as 0 or 1 You will have 2½ hours to complete the examination You may use one page of notes (front and back) on 8½ X 11 paper – You will be asked questions about statistical power, but will not be required to calculate power

32 Case Study

33 Case Study Activity An aid agency implemented a project in Bangladesh with the objective of improving the nutritional and health status of men and women The intervention consisted of a package of services including: nutrition education, primary health care, and other activities To determine whether the intervention might be effective, the project was field-tested in a small rural community prior to large- scale implementation throughout the country A small monetary incentive was provided and slightly more than half of the communitys men and women participated in the study All men and women in the community were weighed prior to the intervention and then were measured for body mass index (BMI) six months after the intervention Those who did not participate were used as a control group and the evaluators found significant improvements in nutritional and health indicators for the treatment group contrasted with the control

34 Questions What is the design of the study? What internal validity threats are most plausible? How might the design feasibly be improved?

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