Research Methods 1 Flashcards

1
Q

clinical decisons should be based on

A

best evidence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what determines the nature/source of evidence needed

A

the problem

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

the best evidence is

A

integrative

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what 4 things should evidence be

A

identified, integrated, appraised and applied

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what should be continuously evaluated ?

A

performance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what 3 things does evidence based medicine incorporate

A
  1. clinician expertise and judgment
  2. hierarchy of medical research evidence
  3. patient values, preferences and experiences
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what does research ethics govern

A

the standards of conduct for researchers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what do research ethics protect?

A

the dignity, rights and welfare of human and animal research participants

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Research ethics approval is provided by a committee…

A
  1. who review a research protocol
  2. to ensure appropriate ethical standards are being upheld
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

which studies require research ethical approvals?

A
  1. studies involving human/animal participantsif-
  2. gathering novel data or information
  3. creating knowledge that can be generalised beyond the participant sample or setting
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

which projects do not require ethical approvals

A
  1. Clinical Audit, as per service evaluation, but evaluating service AGAINST A BENCHMARK (e.g. national standard)
  2. Service Evaluations/Service Improvement/ Quality Improvement, Finds out something about THAT service which can be/is used to improve THAT service
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is exposure

A

risk factor for disease/outcome e.g. gender

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is outcome

A

it is the disease, condition or event of interest e.g. depression

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

prevalence

A

number of people who have disease at given time/number of people at risk of having disease at given time

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Why might we be interested in prevalence

A
  1. informing clinical diagnosis
  2. understanding the disease/condition and its risk factors (exposures) and outcomes
  3. informing prevention and public health interventions
  4. informing service planning and commissioning
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what is a cross sectional study

A
  • it takes place at a single point in time
  • it does not involve manipulating variable but rather, a defined population
  • is surveyed to measure that variable of interest
  • considers sveral characteristics at once
  • prevalence is reported for the sample and/or subgroups based on exposure status
17
Q

strengths of a cross-sectional study

A

Can compare prevalence in exposed and non-exposed to risk factors
Quick and inexpensive study type
Can be used to initially explore/inform a hypothesis, prior to another type of study

18
Q

weaknesses of cross sectional studies

A

Not suitable for rare exposures/outcomes
Cannot separate cause (exposure) and effect (outcome) as they are measured at the same time
Cannot measure rate of new cases arising and any changes therein

19
Q

strengths of primary cross sectional data

A

+ Control over how variable/s of interest measured

20
Q

weaknesses of primary cross sectional data

A

More expensive and time-consuming
Difficult to achieve representative sample

21
Q

strengths of secondary cross sectional data

A

+ Cheap
+ If anonymous, minimal to no ethical/governance approval needed

22
Q

weaknesses of secondary cross sectional data

A

Limited by what data already gathered
Poor accuracy and missing data