L5 14/02 Flashcards

1
Q

For a randomised controlled trial or any experiment gathering new data, what form of data is relied on?

A

Quantitiative

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2
Q

What are experimental designs?

A
  • Dominant method in health research

- Used to test as hypothesis and explain variable relationships

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3
Q

3 key features/assumptions of experimental designs

A

Objectivity, determinism, reductionism

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4
Q

Objectivity definition

A

Reality exists beyond social construction and can be measured

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5
Q

Determinism definiton

A

That the (health) world is governed by natural laws, which are predictable and can be generalised, reasons why everything happens

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6
Q

Reductionism definition

A

The phenomena of interest can be reduced to standard units of measurement

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7
Q

What are the 3 research validities?

A

Internal validity - the study design
External validity - sampling techniques, generalisability
Measurement validity - data collection methods

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8
Q

Why are randomised control trials (RTCs) essential?

A

If the research is explanatory and needs to demonstrate a causal relationship between variables

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9
Q

What do RCTs use to eliminate the effects of confounding variables and biases?

A

Probability sampling, random allocation, and blinding (people aren’t entirely sure which group they are in) to eliminate the effects of confounding variables and biases

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10
Q

What do RCTs aim to do?

A
  • The study design and procedures aim to control for all possible alternative explanations of observed changes in dependent variables
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11
Q

What kind of studies are included in RTCs?

A
  • Field experiments
  • Cohort studies
  • Case-control studies
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12
Q

What are some threats to internal validity in quasi-experiments?

A
  • History: events occurring between pre and post-test measures – only difference between pre and post should be the intervention
  • Testing: the effect of repeated measures on subject responses
  • Regression to the mean: equalisation of measures over time
  • Instrumentation: changes in the measuring tools (or measurers)
  • Selection and interaction biases
  • Mortality: differential ‘drop-out’ rates – will affect ability of data to demonstrate causality
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13
Q

What is a sample?

A

A subset of the population which it is feasible to study. A sample can also be the unit of analysis: a person, an organisation, a body part, anything. The sample is chosen to represent a population.

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14
Q

Give 2 examples of sampling threats

A
  • Sample bias (a population characteristic is over- or under-represented in the sample e.g., volunteer bias)
  • Sample size (too small a sample gives false (unrepresentative) results, unable to make generalisations about whole population)
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15
Q

Definition of random sampling

A

Drawing a specific number from a list of the whole population

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16
Q

Definition of random allocation

A
  • Assigning people in the sample into treatment and control groups
  • Can use a random or non-random sample from the population
  • Random number generator
17
Q

Definition of blinding

A

Where the subjects and / or the researchers do not know who is in the experimental and control groups e.g., placebo or drug

18
Q

Definition of double blinding

A

When BOTH subjects and researchers don’t know who is in which group

19
Q

3 types of experimental design

A
  • Randomised control trials
  • Cohort studies
  • Case control studies
20
Q

RCTs aim to…

A

Eliminate bias and provide valid conclusions

21
Q

What are some key features of RCTs?

A
  • Random allocation to groups
  • Patients and researchers unaware of which treatment was given until the study completed (blinding)
  • Both groups are treated identically except for the experimental treatment
  • Analysis estimates the size of the difference in outcomes between groups AND the statistical power of the effect
22
Q

In quasi-experiments….

A

Participants are NOT randomized to treatment or control groups

23
Q

In cohort studies…

A
  • ABA process
  • Participants are studied over time
  • The study population shares common characteristics
24
Q

In case control studies…

A
  • Studies that address questions about harm or causation
  • Compares different cohorts
  • Investigates why some people develop a disease or behave the way they do vs others who do not
25
Q

What are 7 key factors to consider in experiments?

A
  1. Recruitment methods
  2. Sample size
  3. Randomisation method
  4. Controls and confounding factors
  5. Blinding
  6. Data collection methods
  7. Validity of outcome measures
26
Q

What assumptions are relevant to all forms of experimental designs?

A
  • Objectivity
  • Determinism
  • Reductionism
27
Q

Does a randomised controlled trial NOT require a placebo intervention?

A

False, it is a key attribute of RCT - it does require it

28
Q

Is internal validity in a RCT increased by use of randomisation and blinding?

A

Yes

29
Q

When participants in both intervention and control groups are unaware of which group they are in the study it can be described as double blinding?

A

No it cannot

30
Q

Does a field experiment GUARANTEE causality whereas a RCT can only INFER it?

A

No, a RCT can guarantee causality but field experiment can only infer

31
Q

Would a valid measurement tool will produce the same results on different occasions?

A

No, that’s reliability

32
Q

Does probability sampling decreases the chance of a sample being representative of the population?

A

No

33
Q

What are potential threats to the internal validity of an experimental design?

A
  • Selection bias
  • External events affecting pre and post testing
  • Participant response to being tested