causal research and internal validity Flashcards
CAUSAL RESEARCH AND INTERNAL VALIDITY
descriptive research – gather info (descriptions or measurement) about phenomena
eg. statistics on incidence of eating disorders
causal research – what is cause of illness or other phenomenon
basis to formulate or justify treatment
i.e. provides empirical evidence
CAUSALITY
Criteria:
1. antecedence of cause to effect (C occurs before E)
2. co-variation of cause and effect (if C occurs then so does E)
(or if C increases/decreases then E increases/decreases)
3. elimination of rival causal explanations (if C does not occur then E does not occur)
in general establishing lawful functional relationship between cause and effect
however, relationship doesn’t necessarily mean cause and effect
eg. night follows day (predictable, lawful relationship) but day doesn’t cause night
eg. statistical study – correlation between blood cholesterol and heart disease – alone doesn’t prove cause and effect
Scientific research – look to control phenomena – reproduce or change at will
not always possible (eg. night and day)
therefore – describe patterns/co-variations and formulate hypothesis or theory for cause
attempt to eliminate alternative explanations or hypotheses for cause
THREATS TO INTERNAL VALIDITY
history maturation testing instrumentation regression to the mean selection or assignment errors
compromise conclusion that treatment causes differences or lack of differences observed
i.e. sources of alternative explanation
Threats include:
History – events between pre-test and post-test that are not part of the treatment
eg. initiate low salt diet for hypertension, and patient also starts exercise program
Maturation – time-dependent internal process
eg. infection clearing up by itself
5. Regression to the mean – from unreliability of test measures
eg. choose patient with high cholesterol, second measure more normal
(ie. first measurement abnormally high due to error/fluctuation)
-as increase number of tests, error decreases
6. Selection or assignment errors – groups differ at outset before treatment
eg. assignments not random or low n
7. Mortality (dropout) – if more from one group than other
The dropouts may differ from those that stay, and therefore bias results
history
– events between pre-test and post-test that are not part of the treatment
eg. initiate low salt diet for hypertension, and patient also starts exercise program
Maturation
time-dependent internal process
eg. infection clearing up by itself
testing
practice effects) – repetition of or familiarity with test procedure may change result
eg. familiarity with IQ test may increase performance
Eg. Repetition of test may decreese performance due to fatigue or boredom
instrumentation
- Instrumentation – instrument changes between measurement (reads higher or lower)
- Regression to the mean
– from unreliability of test measures
eg. choose patient with high cholesterol, second measure more normal
(ie. first measurement abnormally high due to error/fluctuation)
- as increase number of tests, error decreases
Selection or assignment errors –
groups differ at outset before treatment
eg. assignments not random or low n
. Mortality (dropout)
– if more from one group than other
The dropouts may differ from those that stay, and therefore bias results
NEED FOR CONTROL
to remove confounding effects of extraneous variables
if can control sufficiently to eliminate other factors has “internal validity”
eg. physicist studying electrical phenomena – insulate against extraneous electrical disturbances
in nutrition research (especially human) sometimes difficult
Control group
ensures/increases internal validity
undergo same conditions as treatment group (except treatment)
eg. given inert tablet or saline injection
with people, must also be cautious of placebo effect
control for placebo effect (need non-treatment group)
-no treatment vs placebo vs treatment
at outset need control and experimental groups as similar as possible
“assignment procedure” – method to assign to control and treatment group
Control
Control a matter of degree rather than absolute
even tightly designed may allow other explanations arising from unexpected factors
trade-off between internal and external validity
ie. control may generalizability to other situations (ecological validity)
therefore may sacrifice some control (internal validity) for ecological/external validity
USE OF CONTROL GROUPS IN CLINICAL RESEARCH
Eg. - redesign, using control group, previous study on exercise in patients with occluded leg arteries
1. sampling – random or matched assignment rather than surgeon’s choice
decrease selection threat
2. pre-treatment test of walking distances for both groups
Decreasing testing threat (since both groups received pretest would be same in both)