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Comparing
  Research
  Designs
                   Patrick Barlow
Statistical and Research Design Consultant, Graduate School of
                         Medicine, UTK
  PhD Student in Evaluation, Statistics, and Measurement, UTK
On the Agenda
 Common problems in research design
     Confounding
     Bias
     Reliability
     Validity


 Observational Research Designs
   Cross-Sectional study
   Case-control study
   Cohort study



 Experimental Research Designs
   Randomized Control Trial
Common Problems in
  Research Design
      Confounding
          Bias
       Reliability
        Validity
Confounding
 A confounder is a variable that is causally
  associated with the outcome (DV) and may or may
  not be causally associated with the exposure (IV)

 Causes spurious conclusions & inferences to be
  made about a set of variables

 Reduced through
    Randomization
    Matching
    Statistically controlling (covariates)
Confounding
           Obesity




PMH Use
                 ?

          Colorectal
          Adenomas
Bias in Research
 The result of systematic error in the design or
  conduct of a study

 Can artificially “trend” results
    Toward the Null hypothesis
    Toward the Alternative hypothesis



 A major problem to consider when planning any
  study
Common Biases
 Selection bias: one relevant group in the population (e.g.
  cases positive for predictor variable) has a higher
  probability of being included in the sample
    Ascertainment: bias in asking questions or offering tests
      of one group over another
 Information: bias from erroneously classifying people in
  exposure/outcome categories
    Adjudication: bias in determining if the treatment was
      helpful due to partial or inadequate blinding
    Recall/Response: bias associated with inaccurate recall
      of exposure or representation of true exposure (self-
      report)
    Experimenter/Interviewer bias: Differential treatment of
      participants in treatment and control groups
 Publication: the tendency to publish only “positive” or
  “significant” findings.
Reliability
• Refers to the consistency of an
  instrument/measurement.

• Thought of as an individual’s “true score” on the
  phenomenon you aim to measure minus
  “measurement error”

• Two common types of reliability
   o Internal consistency: Cronbach’s alpha, KR20
   o Inter-Rater: Kappa statistic


• Necessary but not sufficient in determining validity.
Reliability
Validity
    Refers to the accuracy of an
     instrument/measurement

    In other words, “the degree
     to which you’re measuring
     what you claim to measure”

    Two broad types of validity
       Internal validity
       External validity
Internal Validity
 Concerns the accuracy of measurement within the
  study
 Can be threatened by
   Biases
   Confounding
   History: large scale events that change participants’ attitudes or behavior
    (e.g., recession)
   Maturation: participants change over time, e.g., growth, fatigue etc.
   Repeated Testing: participants get wise to the study and remember the
    test questions
   Compensatory rivalry/resentful demoralization: Control participants work
    extra hard to prove themselves or withdraw because not getting
    treatment
   Diffusion: treatment effects spread from treatment group to control group
External Validity
 The ability to generalize the findings of your study to
  the relevant population.

 Threatened by
      Bias
      Confounding
      Non-experimental design (i.e. case-control vs. RCT)
      Lack of randomization



 External validity is the strongest when a true
  experimental design is used.
Comparing Research
    Designs
      Cross-Sectional Studies
       Case Control Studies
          Cohort Studies
   Randomized Control Trial (RCT)
Pyramid of Clinical
                Evidence
                                                        Evidence
Systematic Reviews                                     Summaries
 & Meta-analyses
                               RCT                     Level 1 Evidence
                               Cohort
                               Studies                    Level 2 Evidence
 Cross-Sectional             Case Control
Studies: Level 2.3             Studies
                                                            Level 3 Evidence
                              Case Series

                             Case Reports

                     Ideas, Editorials, Opinions

                           Animal research

                     In vitro (‘test tube’) research
Cross-Sectional Studies
 “Snapshot” of a population.

 People are studied at a “point” in time,
  without follow-up.

 Strength of evidence…

 What are some research questions that can
  be answered with cross-sectional designs?
Advantages and Disadvantages
       of Cross-Sectional Studies
      Advantages             Disadvantages
 Fast and inexpensive    Can’t determine
 No loss to follow-up     causal relationship
 Springboard to          Impractical for rare
  expand/inform            diseases
  research question       Risk for nonresponse
 Can target a larger
  sample size
Case-Control Studies
 Always retrospective
    Prevalence vs. Incidence



 A sample with the disease from a population is
  selected (cases).

 A sample without the disease from a population is
  selected (controls).

 Groups are compared using possible predictors of
  the disease state.
Advantages and Disadvantages
           of Case-Control Studies
       Advantages               Disadvantages
                            Cannot estimate
 High information yield     incidence of disease
  with few participants
                            Limited outcomes can
 Useful for rare            be studied
  outcomes
                            Highly susceptible to
                             biases
Strategies for Sampling
          Controls
 Population versus hospital/clinic-based controls

 Matching
    Individual level
    Group level



 Using 2 or more control groups
For Discussion
“How much does a family history of
alcoholism increase the risk of being an
alcoholic?” The PI plans a case-control
study to answer this question.
   How should she pick the cases?

   How should she pick the controls?

   What are some potential sources of bias in the sampling of
    cases and controls?
Cohort Studies
 A “cohort” is a group of individuals who are
  followed or traced over a period of time.

 A cohort study analyzes an exposure/disease
  relationship within the entire cohort.

 Groups selected based on exposure to a risk factor.
Cohort Design
Are U.S. Athletes more likely to win a
Group of          gold medal than Chinese athletes at
Interest          the 2012 Olympics?
(U.S.)




       Follow over the games            Compare
                                        Outcomes




Comparison
Group
(China)
Prospective versus Retrospective
        Cohort Studies
                   Exposure           Outcome

                Assessed at the    Followed into
Prospective     beginning of the   the future for
                study (present)    outcome


                Assessed at some Outcome has
Retrospective   point in the past already occurred
Advantages and Disadvantages
                     of Cohort Studies
         Advantages                         Disadvantages
 Establish population-based         Lengthy and costly
  incidence                          May require very large samples
 Accurate relative risk             Not suitable for rare/long-latency
 Temporal relationship inferred       diseases

 Time-to-event analysis possible    Unexpected environmental changes

 Used when randomization not        Nonresponse, migration and loss-to-
  possible                             follow-up

 Reduces biases (selection,         Sampling, ascertainment and
  information)                         observer biases

 Can study multiple outcomes        Changes over time in staff/methods
Randomized Controlled
          Trial
 Considered the “gold standard” by much of the
  research community (level 1 evidence)

  Blind vs. double blind

  Randomization

  Cause & effect
Designs of RCTs
• Parallel Group Trial: Patients in the same
  randomized group throughout the study
• Cross-over Trial: Patient randomly assigned
  to one group then crossed over to other
  group at some point. Patient serves as own
  control – greatly reduces sources of bias
  and confounding
• Factorial Trial: Two or more interventions in a
  single experiment.
Disadvantages of RCT
         Designs
 Extremely time and
  resource demanding

 Unethical in many
  situations

 Poor external validity if
  the RCT is too highly
  controlled

 Difficult to study rare
  events

 Therapeutic
  misconception
Material Learned
       Common problems in research
        design
          Confounding
          Bias
          Reliability
          Validity
       Observational Research
        Designs
          Cross-Sectional
            Studies
          Case Control Studies
          Cohort Studies
       Experimental Research
        Designs
          RCT Design


Questions?
In Pairs…
 Work together to brainstorm an example of how
  your topic could be addressed using 1) a Cross-
  Sectional design, 2) a case-control design, 3) a
  prospective or retrospective cohort design, and an
  RCT.

 Be prepared to share your responses

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Comparing Research Designs

  • 1. Comparing Research Designs Patrick Barlow Statistical and Research Design Consultant, Graduate School of Medicine, UTK PhD Student in Evaluation, Statistics, and Measurement, UTK
  • 2. On the Agenda  Common problems in research design  Confounding  Bias  Reliability  Validity  Observational Research Designs  Cross-Sectional study  Case-control study  Cohort study  Experimental Research Designs  Randomized Control Trial
  • 3. Common Problems in Research Design Confounding Bias Reliability Validity
  • 4. Confounding  A confounder is a variable that is causally associated with the outcome (DV) and may or may not be causally associated with the exposure (IV)  Causes spurious conclusions & inferences to be made about a set of variables  Reduced through  Randomization  Matching  Statistically controlling (covariates)
  • 5. Confounding Obesity PMH Use ? Colorectal Adenomas
  • 6. Bias in Research  The result of systematic error in the design or conduct of a study  Can artificially “trend” results  Toward the Null hypothesis  Toward the Alternative hypothesis  A major problem to consider when planning any study
  • 7. Common Biases  Selection bias: one relevant group in the population (e.g. cases positive for predictor variable) has a higher probability of being included in the sample Ascertainment: bias in asking questions or offering tests of one group over another  Information: bias from erroneously classifying people in exposure/outcome categories Adjudication: bias in determining if the treatment was helpful due to partial or inadequate blinding Recall/Response: bias associated with inaccurate recall of exposure or representation of true exposure (self- report) Experimenter/Interviewer bias: Differential treatment of participants in treatment and control groups  Publication: the tendency to publish only “positive” or “significant” findings.
  • 8. Reliability • Refers to the consistency of an instrument/measurement. • Thought of as an individual’s “true score” on the phenomenon you aim to measure minus “measurement error” • Two common types of reliability o Internal consistency: Cronbach’s alpha, KR20 o Inter-Rater: Kappa statistic • Necessary but not sufficient in determining validity.
  • 10. Validity  Refers to the accuracy of an instrument/measurement  In other words, “the degree to which you’re measuring what you claim to measure”  Two broad types of validity  Internal validity  External validity
  • 11. Internal Validity  Concerns the accuracy of measurement within the study  Can be threatened by  Biases  Confounding  History: large scale events that change participants’ attitudes or behavior (e.g., recession)  Maturation: participants change over time, e.g., growth, fatigue etc.  Repeated Testing: participants get wise to the study and remember the test questions  Compensatory rivalry/resentful demoralization: Control participants work extra hard to prove themselves or withdraw because not getting treatment  Diffusion: treatment effects spread from treatment group to control group
  • 12. External Validity  The ability to generalize the findings of your study to the relevant population.  Threatened by  Bias  Confounding  Non-experimental design (i.e. case-control vs. RCT)  Lack of randomization  External validity is the strongest when a true experimental design is used.
  • 13. Comparing Research Designs Cross-Sectional Studies Case Control Studies Cohort Studies Randomized Control Trial (RCT)
  • 14. Pyramid of Clinical Evidence Evidence Systematic Reviews Summaries & Meta-analyses RCT Level 1 Evidence Cohort Studies Level 2 Evidence Cross-Sectional Case Control Studies: Level 2.3 Studies Level 3 Evidence Case Series Case Reports Ideas, Editorials, Opinions Animal research In vitro (‘test tube’) research
  • 15. Cross-Sectional Studies  “Snapshot” of a population.  People are studied at a “point” in time, without follow-up.  Strength of evidence…  What are some research questions that can be answered with cross-sectional designs?
  • 16. Advantages and Disadvantages of Cross-Sectional Studies Advantages Disadvantages  Fast and inexpensive  Can’t determine  No loss to follow-up causal relationship  Springboard to  Impractical for rare expand/inform diseases research question  Risk for nonresponse  Can target a larger sample size
  • 17. Case-Control Studies  Always retrospective  Prevalence vs. Incidence  A sample with the disease from a population is selected (cases).  A sample without the disease from a population is selected (controls).  Groups are compared using possible predictors of the disease state.
  • 18. Advantages and Disadvantages of Case-Control Studies Advantages Disadvantages  Cannot estimate  High information yield incidence of disease with few participants  Limited outcomes can  Useful for rare be studied outcomes  Highly susceptible to biases
  • 19. Strategies for Sampling Controls  Population versus hospital/clinic-based controls  Matching  Individual level  Group level  Using 2 or more control groups
  • 20. For Discussion “How much does a family history of alcoholism increase the risk of being an alcoholic?” The PI plans a case-control study to answer this question.  How should she pick the cases?  How should she pick the controls?  What are some potential sources of bias in the sampling of cases and controls?
  • 21. Cohort Studies  A “cohort” is a group of individuals who are followed or traced over a period of time.  A cohort study analyzes an exposure/disease relationship within the entire cohort.  Groups selected based on exposure to a risk factor.
  • 23. Are U.S. Athletes more likely to win a Group of gold medal than Chinese athletes at Interest the 2012 Olympics? (U.S.) Follow over the games Compare Outcomes Comparison Group (China)
  • 24. Prospective versus Retrospective Cohort Studies Exposure Outcome Assessed at the Followed into Prospective beginning of the the future for study (present) outcome Assessed at some Outcome has Retrospective point in the past already occurred
  • 25. Advantages and Disadvantages of Cohort Studies Advantages Disadvantages  Establish population-based  Lengthy and costly incidence  May require very large samples  Accurate relative risk  Not suitable for rare/long-latency  Temporal relationship inferred diseases  Time-to-event analysis possible  Unexpected environmental changes  Used when randomization not  Nonresponse, migration and loss-to- possible follow-up  Reduces biases (selection,  Sampling, ascertainment and information) observer biases  Can study multiple outcomes  Changes over time in staff/methods
  • 26. Randomized Controlled Trial  Considered the “gold standard” by much of the research community (level 1 evidence) Blind vs. double blind Randomization Cause & effect
  • 27. Designs of RCTs • Parallel Group Trial: Patients in the same randomized group throughout the study • Cross-over Trial: Patient randomly assigned to one group then crossed over to other group at some point. Patient serves as own control – greatly reduces sources of bias and confounding • Factorial Trial: Two or more interventions in a single experiment.
  • 28. Disadvantages of RCT Designs  Extremely time and resource demanding  Unethical in many situations  Poor external validity if the RCT is too highly controlled  Difficult to study rare events  Therapeutic misconception
  • 29. Material Learned  Common problems in research design  Confounding  Bias  Reliability  Validity  Observational Research Designs  Cross-Sectional Studies  Case Control Studies  Cohort Studies  Experimental Research Designs  RCT Design Questions?
  • 30. In Pairs…  Work together to brainstorm an example of how your topic could be addressed using 1) a Cross- Sectional design, 2) a case-control design, 3) a prospective or retrospective cohort design, and an RCT.  Be prepared to share your responses

Editor's Notes

  1. Most of this presentation will address the observational research designs because those are the ones students will see most often in their own work (most likely). I briefly touch on the common problems in research design as well as a couple of different RCT designs.
  2. The focus is not to give an in depth description of confounding because you will be hitting it on a separate lecture. I just need to introduce a couple of these concepts so describing the strengths and weaknesses of the various designs can be clearer.
  3. Using one of the example findings from this week’s article to illustrate confounding.
  4. Very general introduction to bias. I will be asking the class to think of possible sources of bias before moving to the next slide.
  5. Would love any examples you may have for these biases based on your area of research.
  6. I’m using a social science version of these constructs, but from what I see Epi/Med lit uses “precision” and “accuracy” in place of reliability and validity.
  7. Since the Olympics are likely still fresh on everyone’s minds, and I coached/played the sport for many years, I have this example of inter-rater inter-observer reliability as the judging for Olympic gymnastics.My more professional examples are:Multiple judges for professional presentations (we have to calculate it every year for our annual residents’ research day)Multiple physicians looking at the same x-ray or CT (have several stories about those)Multiple scorers on the same essay (e.g. the ACT or GRE writing portion)Doctoral/Master’s committees (while they don’t calculate it, the example still makes sense)
  8. Archery is a classic example of validity, and again I went with the Olympic theme for fun.While there are numerous types of validity, I choose to briefly hit on internal and external as they are most related to experiments/studies themselves.
  9. Several of these have great Public Health implications such as History.
  10. Cross-sectional Studies considered 2.3 by the OBGYN journal I looked at, but it is not technically a “Clinical” study.Double check to see if this is the same pyramid of evidence you see used in Epi.
  11. Can measure attitudes, beliefs, behaviors, personal or family history, genetic factors, existing or past health conditions, or anything else that does not require follow-up to assess.The source of most of what we know about the population.Before moving to the next slide I will be asking for some students to discuss what they think could be drawbacks of these designs.
  12. For each of these study types I like to layout the advantages and disadvantages for students to easily see.
  13. I ran into an incidence v prevalence situation with two students on Wednesday, so hitting it here will be good.The largest yet simplest factor in differentiating case-control from cohort is in the way the groups are selected. That has been the best way for me to describe it to students in the past.
  14. Discuss advantages/disadvantages of each. I have examples of how each would be done.
  15. I would be VERY open to suggestions as to what a more relevant example would be for these students.
  16. Another Olympic example for fun.
  17. I find that people oftentimes get confused on figuring out how these are separated. I usually say that in a retrospective you start in the past and work towards the present while in a prospective you start in the present and work towards the future.
  18. Before showing the slides, have the class brainstorm what some of the possible Pros and Cons to a cohort study could be. After we go through them in class, have them get with a partner to try and think of ways to avoid some of the cons.
  19. This part of the presentation is meant to introduce RCTs, and some of the language associated with them. It is by no means meant to be a all-encompassing presentation on the topic.
  20. Therapeutic misconception: control patients believe they are getting the best treatmentRegarding the external validity comment: I plan to acknowledge that both types of validity are high in RCT designs; however, the more like a laboratory you make an experiment (i.e. the more controlled it is), the less it is reflective of how things work in the real world.