Study Designs Flashcards

1
Q

Ecological

A

Population-level data
eg electoral role

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2
Q

Ecological advantages

A

Fast
Inexpensive
Few ethical issues
Data collection fairly easy
Can look at trends between regions or over time

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3
Q

Ecological Disadvantages

A

Cannot determine individual-level associations
Cannot demonstrate cause and effect
Lack of control over variables collected

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4
Q

Cross-sectional

A

Outcome and exposure status measure simultaneously

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5
Q

Cross-sectional advantages

A

Can look at associations- hypothesis generating
Data collection fairly easy
Can study multiple exposures and outcomes
Fast
Inexpensive

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6
Q

Cross-sectional disadvantages

A

Cannot demonstrate cause and effect
Prone to bias and confounding
Not useful for rare exposures or outcomes

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7
Q

Case-control

A

Participants selected on the basis of outcome

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8
Q

Case-control advantages

A

• Can look at association between outcome and prior exposures
• Fast
• Inexpensive
• Good for studying rare outcomes
• Can study multiple exposures

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9
Q

Case-control disadvantages

A

• Cannot determine incidence/risk of outcome
• Limited control over data quality – poor historic records or recall bias
• Retrospective nature limits ability to determine causality
• Not useful for rare exposures

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10
Q

Cohort

A

Participants selected in the basis of exposure

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11
Q

Cohort advantages

A

• Can look at incident cases and associations with exposure
• Good for studying rare exposures
• Can study multiple outcomes
• Control over data collected
• Exposure determined before outcome occurs so can demonstrate temporality for potential cause and effect

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12
Q

Cohort disadvantages

A

• Mostly prospective which can be time consuming
• Risk of loss to follow-up
• Expensive
• Not useful for rare outcomes

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13
Q

Randomised controlled trial

A

Participants randomly allocated to interventions then followed up to compare outcomes
Experimental study with random allocation into treatment groups (NOT random sampling)

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14
Q

RCT advantages

A

• Can study intervention effects on outcome(s)
• Random allocation means confounding factors should be evenly distributed
• Control over variables collected
• Comparator group means ability to account for placebo/temporal effects
• Less prone to bias, particularly where blinding and objective outcome assessment used
• Gold standard for establishing causality- can show cause-effect relationship

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15
Q

RCT disadvantages

A

• Time consuming
• Expensive
• Require expertise to run
• Can only be used where ethics and participant willingness permit randomisation to intervention
• Overly strict eligibility criteria may render sample not fully representative of population
Affected by non-compliance
Not practical for long-term effects

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16
Q

Case control studies can only use…

A

Odds not risks

17
Q

Three-arm trial

A

a 3-arm trial consists of the intervention, the active control, and a placebo arm. This design is particularly attractive when the efficacy of the active control has changed, is volatile, or is in doubt

18
Q

Cluster randomisation

A

a randomised controlled trial in which pre-existing groups, called clusters, of individuals are randomly allocated to treatment arms. For example, clusters may be clinical practices or schools where the individuals are patients and school children, respectively.

19
Q

2 characteristics a placebo treatment should have

A
  1. Inactive form of ingredients
  2. Identical look and administration of treatment
20
Q

Blinded

A

Participants do not know whether they receive treatment or placebo

21
Q

Random assignment

A

Assignment is unpredictable and equal probability of ending up in either group

22
Q

Hierarchy of evidence

A
  1. Systematic review of RCTs
  2. RCT
  3. Cohort
  4. Case control
  5. Cross-sectional
  6. Case series
  7. Anecdote
23
Q

2 types of observational study

A

Descriptive and analytical

24
Q

Descriptive study : individuals

A

Case report
Case series

25
Q

Descriptive study : populations

A

Ecological study
Cross-sectional study

26
Q

Single time point analytical study

A

Cross-sectional study- population: see how many have disease and how many have symptoms
Exposure <-> outcome

27
Q

Retrospective analytical study

A

Case-control study- compare prevalence of symptoms in control vs disease group
Outcome —> exposure

28
Q

Prospective analytical study

A

Cohort study- sample of unaffected and measure exposure to risk factor over time
Exposure —> outcome

29
Q

Experimental intervention study

A

Randomised controlled trial

30
Q

Types of RCT

A

Cluster
Crossover
Multi-arm + factorial
Adaptive

31
Q

Cluster RCT

A

Randomise groups rather than individuals

32
Q

Crossover RCT

A

Receive both interventions in randomised order
ONLY if incurable or chronic

33
Q

Multi-arm + factorial RCT

A

> 1 interventions compared

34
Q

Adaptive RCT

A

Accruing information informs study eg early termination I’d clear treatment difference