• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/40

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

40 Cards in this Set

  • Front
  • Back
Variable
Characteristic that takes on different values in different persons, places or things. Able to quantify information
Discrete variable
characterized by gaps or interruptions in values that it can assume
Example: # of siblings = must be 0, 1, 2, 3, 4…… it cannot be 5.3 siblings
Continuous variable
variables that can take on any value

Ordinal variables are usually considered continuous
Categorical Variables
Must assign a number to, but that number in itself means nothing
Independent Variables
These are “manipulated” by the experimenter

Ex: In epidemiology the exposure is the independent variable and the disease or outcome is the dependent variable
Dependent variables
are the outcome
Regression is as simple as Y=mx + b
X=independent variable; y= dependent variable
Study Design Sequences
used to answer research questions, and create new knowledge
Case-series Study Design
-A series of cases
-No control/comparison group
-Cannot calculate relative risk, attributable risk or odds ratios
-Cannot makes statements about preventing disease
-Causation cannot be shown
Ecological Study Design
-Compare groups, but do not have data on individuals
-Used to generate rather than test hypotheses
-Apt to ecological fallacies
Cross-sectional study
-Observational, no intervention
-Effective at providing a picture of disease, health or psychological phenomenon
-effective at assessing several variables at once and associations between those variables
Cross-sectional study
-Disease and exposure data collected simultaneously
-Can determine distribution of disease and exposure
-Problem: Temporal sequence not always known (ex: runners/thin)
Case-control or retrospective study
-Observational
-Compare the past exposures of cases and controls
-Collect data after onset of disease & Look backward in time to find the exposure
Prospective studies or “cohort studies”
-All subjects are “well” at the onset
-Data collected before the disease, temporal sequence known
-Provides incidence data
-Divide on some exposure (ex: smoking) and look for outcome in future
Experiments
-intervention occurs
-randomization and manipulation
Quasi experimental design
-there is manipulation but not randomization
Cohort studies
-Cohorts are cohorts because of some common exposure
-Follow forward in time and look for an outcome
-Gets incidence rates
-Can add new exposures/outcomes
-Temporal sequence know
Relative Risk
Shows strength of association of exposure and disease
Relative Risk
-if RR > 1.0 then the factor is said to be causative
-if RR= 1.0 the factor is unrelated to the disease, "the factor is just as likely to occur among those with the factor as those without it"
-if RR< 1.0 the factor is said to be "protective”
Attributable Risk
-measure of how much disease could be eliminated if the exposure was not present
-estimates the proportion of disease among the exposed that is attributable to the exposure or the proportion of the disease that could be eliminated if people did not
Population attributable risk
-indicates the proportion of all cases in the total defined population that can be ascribed to a factor
-the % of disease among the entire population that can be attributed to the exposure
Bias in case control studies
*selective memory- those with the disease remember better than those without
*Selective survival-the result of differences between those who survive and those who live
Odds ratio
-an estimate of the relative risk, will be similar unless the incidence is high in the exposed group
internal validity
can we ascribe the observed effect to the exposure / variable under investigation
External validity
do the results apply to others or other situations? Can we generalize the results beyond the observed findings to some universal statement?
7 main threats to validity
1. Testing: people improve over time
2. Instrumentation: same instruments should be used
3. Maturation: Over time people mature and maturation will change them whether or not they are in your study
4. Regression toward mean
5. Selection bias
6. History: Outside interference to study
7. Attrition: drops out of study
bias
misclassify variables in a consistent way that tips the scale in a certain direction
Reliability
-measure of consistency & repeatability
- Does NOT mean accuracy
Inter rater reliability
results might differ when 2 or more people rate something
Intra rater reliability
-same person rates observations
- same person might rate things differently
Calculate Inter rater reliability & Intra rater reliability
# agreements / total # of possible combinations
Validity Components
sensitivity & specificity
sensitivity
if you have the disease/outcome how accurate is your measurement instrument in identifying that
specificity
if one truly doesn't have the disease, how well does the measurement tool accurately detect no disease.
Calculate sensitivity
(true positives) / (true positives + false negatives)
Calculate specificity
true negatives / all that are truly negative
Positive predictive value:
Proportion of true positives among those who test positive
a / (a + b)
Negative predictive value
proportion of true negatives out of the total who test negative
d / (d + c)
Confounding
occurs when the crude odds ratio or RR differs from the adjusted ones
occurs we say that an interaction has occurred
interaction
occurred when a variable affects an outcome differently at different levels of another variable