Math 151 , Fall 2002, Friday Day 19, Oct. 11 Hit reload to get most current versionAfter Class



HW assignment Day 19
Reading:  Finish 3.1, next 3.2 up to Matched Pairs, p. 196 (Statistical Significance, Matched Pairs and Block design after)
Hand in Wednesday
Sampling
p. 185 3.30 survey questions
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p. 181  3.16 bigger sample size
p.185 3.31 sampling error for men
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Probability Samples (other):  from Moore
 p. 176 3.11 stratified sample, accounts 
 3.12 multistage design, schoolkids 
 p. 184, 3.27 Systematic.
 3.28 same chance for each.  SRS?
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 Postpone
Design of experiment: All from Moore
p. 200, 3.46 experiment?
p. 187, 3.32 sickle cell
p. 188, 3.34& p. 209 3.70 chemical reaction (randomize order)
    Also: Does this experiment have a Control/Baseline group?
p. 192  3.37  child care, recruitment(randomize)
    Use a diagram like those on pp. 190-1 to show your design.
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Control, randomization, replication 
p. 194  3.38 
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Cautions (blinding, lack of realism) 
p. 196 3.42  pain reliever
p. 202 3.55 placebo effect
p. 208 3.75 reading medical jl
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Hand in Friday: answers to these questions on the "Placebo Effect" article (outside my door/on reserve): 
a) Give two examples of the placebo effect 
b) What do researchers believe causes the placebo effect? 
Read, to discuss 
Sampling
p.180 3.14 ring-no-answer
3.15 2 campaign questions
 
 
 

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p. 194 3.39 exercise/heart

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3.41meditation/anxiety
p. 202, 3.52 sickle cell 

Optional 
 
 
 
 

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p. 187, 3.33 sealing food
p. 192, 3.36 ditto
 

ACT p. 11-3.  Doing and analyzing an experiment, activities 1 and 2.  Save your SPSS data file for future use.
(Activity 3 is optional: Note, this activity shows the situation  of a continuous range of treatment levels; we won't be discussing that situation.)

Sampling, cont'd
More kinds of probability samples:
We will focus on the mathematics of the SRS, the most basic.  In practice, more sophisticated sampling methods may be preferred.  The math needed to analyze their effects is beyond our course.
   Here are some other ways to design a probability sample:
Stratified Random Sample: population is cut into natural segments ('strata').  A specific number of individuals is chosen from each stratum (within each stratum we take a simple random sample).  Advantage: Every stratum is represented with a known proportion of the sample; a simple random sample might under- or over-represent a stratum, by chance.

Multistage Sample: Useful when individuals are at the bottom of a sequence of categories: E.g. to choose a sample of college women, first select 10 colleges, at random, then from those colleges select 2 dorms at random, then from each dorm select 10 students to interview.  Total sample = 200.  Advantage: you only have to visit 10 colleges, 2 dorms in each.  An SRS from the whole country, even if you could do it, might mean 200 colleges.  (You can also mix this with stratification, for instance selecting the 10 colleges in a stratified way from large coed, small coed, womens,...)

Systematic Random Sample (p.184, problem 3.27)  Using a list, to pick a sample of 1/20 of the list: First pick a number at random from 1,2,....20.  Suppose you get 8.  The 8th individual in the list is the first one in the sample.  Then take every 20th individual after that, numbers 28, 48, 68,....   Advantage: Easy to implement, avoids "clumps" that might occur with SRS.

Sources of bias, even in probability samples:

Inference to the population: Sample results will vary.
   Different samples will represent the population with differing accuracy.
   Well-designed Random (probability) sampling will avoid systematic bias.
   In general,  A larger random sample will give more accurate information about the population than a smaller random sample.
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Start here Wednesday
"Convenience Sample/ Voluntary Response Sample/ Sampling Frame/ Nonresponse bias"--relationships.
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Ch. 3.2 Designing Experiments
         Observational Study   vs. Experiment  day 18
                Different jargon; different traditions.

Do something to:
    "Experimental Units" = "Subjects"
Treatment:  Specific experimental condition.
Factor: Explanatory Variable we manipulate.
    Levels: Specific values of a factor that we set.
Response variable(s)

E.g. 2 headache medications, in combination?
A two-factor experiment, each with 3 levels. 9 possible treatments.
    Factor A: Aspirin:  levels None, 500 mg, 1000 mg
    Factor B: Caffeine: levels None, 50 mg, 100 mg
Response variable: reported pain relief
Aspirin
None 500 mg 1000 mg
None Treatment 1 Treatment 2 Treatment 3
Caffeine 50 mg Treatment 4 Treatment 5 Treatment 6
100 mg Treatment 7 Treatment 8 Treatment 9

Lurking variables:  Control--how?  Nothing except experimental treatment should affect response.
    Compare responses under several treatments, look at differences.
Placebo effect: a positive response to a "sham" medical treatment--if you believe it will work, it very likely will. (Tinkerbell?)
    A medical treatment must be shown to be better than a placebo (at least) to be approved by the FDA.
        (Cf. "Claritin," Sunday NYTimes magazine, March 11, '01)
        placebo="I shall please" (Latin)
To control for the placebo effect, All treatments should "look alike".  Treatment 1 above should be a pill with no medicine--a "placebo".  (Some experiments even try to duplicate side effects of actual medication.)

"Control group" Group that gets the "baseline"--"null"-- "none" or "placebo" level of the factor.  Should be "just like" the group(s) that get the "treatment" ("real" levels of the factor).  So Treatment 1 above will go to the "control group", the other 8 will go to "experimental" or "treatment groups."
Murky language here:  "Experimental vs. control" or "Treatment vs. control" is different usage from "Treatments", one of which is the "control"="none"/"placebo".
     *Sometimes the Control  is the current "best practice" treatment, rather than none.

How to get groups "just like" one another?  Randomize who goes into which group.  (Usually our batch of  experimental units is not a random sample from the population of all individuals--volunteers, etc.)
Randomized comparative experiment : Diagrams of design, Moore pp. 140-141
Completely randomized: all exp. units allocated at random among the treatments.

E.g. does acupuncture work for PMS?  Response: report of symptoms.
    One factor, 3 Levels:  None (music?), Acupuncture (wrong places), Acupuncture (right places). 3 treatments.
            (control(s)?)
      30 subjects with PMS:  Randomize, 10 each treatment.  Administer treatments.  Compare symptoms. (Do diagram)

Picking groups with random number table:  Pick "sample" of size 10 from the 30 for first treatment.  Pick another "sample" of size 10 for 2nd treatment, from the remainder.  The 10 remaining get the 3rd treatment.

Why 10 each, not just 1 each?  Replication of the experimental treatments on many units allows "averaging out" chance variation in the units.  (Don't confuse the replication needed within one experiment, with "replication" of the whole experiment in a different time and place to confirm its results.)

Principles of designing an experiment (p. 143) See above

More problems, cautions:
Placebo and biasing effects can result from expectations of medical staff.  "Blind" means subject doesn't know who's getting "real" treatment.  "Double blind" means neither subject, nor staff administering treatment, nor people recording response variables know who's getting which treatment. (That should really be triple blind?) Most convincing for cause/effect.

Lack of realism Do sociology, psychology experiments generalize to "real life?"  Ethical questions...


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