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target population
largest group, to whom you intend to apply result of the study
accessible population
group must be accessible to you
collect your sample from this group
representative of target pop
sample
group that participate in study
probability sampling
allows everyone from accessible population to have equal chance of being selected
examples of probability sampling (4)
simple random sample
systemic sample
stratified random sample
cluster sample
non probability samples
do not give everyone from the accessible population an equal likelihood of being selected
which type of sampling used more common in health care
nonprobability
which type of sampling reduce error and bias
probability
examples of non probability (4)
convenience sample
quota
purposive
snowball
convenience sample
Participants chosen based on availability to be included
consecutive sample involves recruiting everyone
volunteers may be recruited by announcing the study and requesting those interested to participate
quota sample
non-random stratified sampling
quota established from different strata to match the sample to the population
purposive sample
researchers purposely select participants based on characteristics desired for the sample
snowball sample
used for rare or sensitive topics
after initial group is selected to participate, they are asked to identify others who meet criteria, who are then invited to participate
simple random sample
all indiv are included in the pool as a random selection occurs
systematic sample
when there is non ordered list available, every nth indiv is selected
stratified random sample
to improve representativeness (decrease sampling error), strata are created that relate to the accessible population
random sample within each strata
cluster sample
when accessible population is large, it is grouped into cluster
random selection of cluster is made and then population of the cluster, or a random selection of those within the cluster is sampled
the flaw in bias is ….
systematic
misclassificaion bias
participants are not correctly classified as having or not having a quality, based on poor operational definition
recall bias
participants recall (or do not) historical facts based on wanting to identify a relationship (or not)
reporting bias
participants in one group systematically underreport/overreport an exposure or outcome
sampling bias
the sample is no representative of the accessible population for a systematic reason (not by chance)
allocation bias
in nonrandom samples, when individuals with certain qualities are represented differently in groups
examples of primary research
research conducted with patients
observational research
experimental research
observational research
describes group of indiv on different variables
may be based on an individual, a single group, or more than one person
some separate descriptive research out as a sep category, while other include it as observational
experimental research
experimental designs used to compare two or more different conditions/interventions to assess efficacy
examples of secondary research
research is conducted on the results of primary research
researchers not working with patients
synthesis research
synthesis research
combines results of various other studies to provide stronger evidence
examples of observational study design (4)
case studies
case report
case series
cross-section studies
case-control studies
cohort
examples of experimental study design (1)
randomized control trials
what does pyramid of evidence tell us
how common
validity
what type of evidence best in treating patients
systematic review and meta-analysis
observational studies
primary study design
used commonly in epidemiology
helpful discover new info
researcher doesnt have large amount of control
doesnt determine cause and effect
which study mostly used in epidemiology
observation
case studies (2 types)
*lowest on evidence pyramid
case report (indiv)
report of single patient with unique phenomenon
case series (group)
report of a group of patients all with same or similar unique phenomenon
what is the least valid approach to determining cause because of competing variables and lack of control
case studies
why are case studies useful
understand new and unusual presentations of conditions we already know about
identify new treatments for both existing and new conditions
discover new conditions that were previously unknown
begin to develop hypotheses for testing with other study designs
case studies objective
describe individuals with disease
case studies population
all included indiv with same disease
when is case study used
patient or group is available with no comparable group
caution with using case study
lack of generalizability
statistical measures of case study
descriptive statistics
cross-sectional studies
observational study that measures the association of an exposure to the presence or absence of a disease at a particular point in time
capture moment in time, nothing historical or future
surveys are examples of
cross-sectional studies
objective of cross-sectional studies
describe exposure or disease status of a population at a moment in time
population of cross sectional studies
study participants must be representative of source population
when is cross section study used
time or budget limited
what to be careful of with cross sectional study
sample is not representative of pop
statistical measure of cross-sectional study
prevalence, linear regression (r)
case-control study
observational study when we compare
cases- indiv with the phenomenon of interest, and
controls- indiv without phenomenon of interest
gives retrospective
Investigate previous exposure or risk factors
*study design is retrospective
case matching
individual (case) and examine controls and try to match in as many dif ways as possible
Ex: patient is F, native american, 60s, diabetes. what is risk factor smoking and COPD, look for control similar age, ethnicity
objective of case control studies
comparing exposure histories of people with and people without a disease
population of case control studies
cases and controls must be similar, aside from disease state
when is case control study used
disease is uncommon, long induction period, or little is known but a source of cases is available
what to watch out for with case control studies
recall bias
statistical measure of case control studies
odds ratio
cohort studies
can be prospective or retrospective
observational
prospective study vs retrospective
begins after exposure /risk/intervention and follows groups forward in time
looks for groups with conditions, and then looks even further back to establish a baseline
difference btw cohort and case control
cohort studies groups people by risk/intervention and look for disease, where case control group by disease and look for previous risk/exposure
objective of cohort
compare rate of disease overtime in people with or without particular exposure
population of cohort study
participants must be similar except for exposure status, and not have the disease at the start
when is cohort study used
exposure is somewhat common and there is group available
what do you watch out for with cohort study
loss to follow up (prospective) and missing records (retrospective)
statistical measure of cohort
relative risk ratio
randomized control trials
experimental designs require an intervention, control, and assignment to group
two key elements of randomized control trials (RTC)
key elements are randomization and control
T/F control group is always placebo
F
randomization
participants assigned to groups by chance- the researchers do not select who will be assigned to what group
T/F blinding and randomization are the same
F- there can be randomization without blinding, and there can be blinding without randomization
what allows for cause and effect relationship
randomization
equal likelihood confounding variables spread across groups
key concepts in RTC (4)
rigorous selection of subjects
specific protocol and measurement
specific measurements
blinding
objective of RTC study
compare outcomes btw those assigned to an intervention and those assigned to a control
population of RTC study
similar participants assigned to each group
when is RTC study used
to assess for cause/effect
what to watch out for with RTC
non compliance
statistical measure of RTC
efficacy, risk
what does CONSORT diagram help determine in RTC study
how patients move through a study
ex: how many pt lost in study?
systematic review
secondary research
study question and inclusion/exclusion criteria defined
extracted primary study results are raw data for this primary research
extensive search of literature
objective of systematic review
synthesize existing knowledge
population of systematic review
published literature
when is systematic review used
to compare findings of previously conducted studies on a specific topic
what to watch out for with systematic review
publication bias
statistical measure of systematic review
none, but may report measures from included studies
meta analysis
type of systematic review
uses only studies with quantitative results
summary statistic from each included study is included that is then analyzed with other statistics from primary studies
objective of meta anlysis
synthesize existing knowledge
population of meta analysis
published literature
when is meta analysis used
to compare findings of previously conducted studies on a specific topic using pooled statistics
what to watch out for with meta analysis
publication bias, studies that cannot be fairly compared
statistical measures of meta analysis
summary measure
experimenter effect (internal validity threat)
researcher could treat participants differently if they knew what group the participants were in therefor affecting the participants behavior
observer bias (internal validity threat)
when the researcher knows the hypothesis and variables of the study and has a biased view because they know what they are looking for
researcher attribute (internal validity threat)
how the characteristics of the researcher can affect the participants (example how they look, gender)
hawthorne effect (internal validity threat)
participants responses change because they know they are being observed, similar to the social desirability effect
testing effect (internal validity threat)
taking a pretest before the experiment can influence the participants views which confounds the experimental results internal validity that the conclusions drawn from experimental results accurately reflect the experiment
maturation (internal validity threat)
people and their surroundings are continually changing, and such changes can effect the experiment
experimental mortality (internal validity threat)
people drop out of experiment before it is complete (like if there was a smoking psa experiment, the kids who already smoke might just leave)
selection bias (internal validity threat)
comparisons between two groups of participants means nothing unless these groups are essentially the same at the beginning of the study (random sampling helps us ensure they will be)
intersubject bias (internal validity threat)
when participants from the control group and the experimental group have accesses to one another and can share information
compensatory rivalry
those in the control group may try to compensate for lack of stimulus and work harder that normal
demoralization
feelings of being denied in the control group may result in them just giving up