Blinding
Not telling someone what treatment a person has received/outcome of the treatment
Avoid them being influenced by knowledge
Case control study
Used to identify risk factors for a condition
Cluster randomised control trial
People are randomised in groups or clusters rather than individually
Cohort study
Identifies a group of people and follows them over a period of time to see how their exposure affects their outcome
Confidence interval
Expresses the precision of an estimate and shows a range within which we are 95% sure the true value from the results fo a population lies
Narrower = more precise estimate
Confounding factor
Something associated with both the exposure and the outcome of interest but is not the causal pathway between them
Control group
Serves as a basis for comparison in a study. In this group no experimental stimulus is recieved
Epidemiology
The study of factors that affect the health and illness of the population
Experiment
Any study in which the conditions are under the direct control of the researcher. Usually involves giving a group of people an intervention that would not have occurred naturally
Hazard ratio
Measure of the relative probability of an event in 2 groups over time.
Takes into account the fact that once people have a certain event (eg death) they are no longer at risk of that event
Intention to treat
People are analysed in the treatment groups to which they were assigned to at the start of the RTC regardless of whether they drop out, dont attend follow up/switch treatment groups
Levels of evidence
Hierarchical ranking of different types of clinical evidence
High - low: systematic review, RTC, non randomised RTC, prospective cohort, case-control
Longitudinal study
One that studies a group of people over time
Meta-analysis
Combines the results of individual studies to arrive at one overall measurement of the effectiveness of a treatment
Nested case control study
Cases of a disease are drawn from the same cohort as the controls to which they are compared.
Can reduce recall bias and temporal ambiguity - where its unclear if a hypothesised cause preceded the outcome
Non randomised study
Participants are not randomly allocated to receiving/not receiving an intervention
Observational study
Researchers have no control over exposures and instead observe what happens to groups of people
Odds ratio
Summarises the association between an exposure and an outcome
Tell us how likely it is that an event will occur compared to the likelihood the event will not happen.
Person years
Describes the accumulated amount of time that all the people in the study were being followed up.
Phase 1 trials
Early phases of drug testing in humans. Usually quite small
Tests drugs safety as opposed to effectiveness
Phase 2 trials
Drugs effectiveness in treating targeted disease is examined for the 1st time
Phase 3 trials
Effectiveness and safety of the drug undergoes a rigorous examination in a large carefully controlled trial.
Usually compare with existing drug/placebo
Prevalence
Th amount of people who currently have a disease in a set population with no time frame
Prospective study
Asks a specific study question, recruits appropriate participants and looks at the exposures and outcomes of interest in these people over the following months/years