1 Flashcards

1
Q

what is postive control group should have

A

should show a particular change during the experiment

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2
Q

postive control

A

a group in an experiment that receives a treatment with a known result, there fore should show a particular change during the experiment

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3
Q

positive control group is used for

A

1used to asses test validity so to asses a new test’s ability to setect a disease = sensitivity
2Used to control for unknown variables during experiment
3to give the scientist something to compare with the test group

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4
Q

negative control are

A

groups where no phenomenon is expected, they ensure that there is no effect when there should be no effect

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5
Q

postive and negative control group are used for

A

Used to eliminate most potential confounding variables

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6
Q

Vehicle control

A

is a solution that contains everything but the test substance you are evaluating

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7
Q

characterise of vehicle control

A

Often times you may need to use solubilizing factor or reduced pH or ethanol to solubilize your drug

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8
Q

Sham or procedural control

A

a control that has the exact same procedure performed without the factor be evaluated

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9
Q

how to overcome Sham ethical issue

A

In many clinical trials you can run a comparative effectiveness study where you compare your new drug or procedure to the current standard of care.

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10
Q

Complete Randomized Design

A

All subjects are assigned randomly to a group or groups and then the IV is randomly assigned to each group.

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11
Q

Factorial Designs

A

One of the more common designs used in experiments. The simplest being a comparison between a treatment and a control. This would be a 1 x 2 factorial design

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12
Q

. Traditional dose-response curve is

A

a 1 x 6 factorial design

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13
Q

Factorial designs can also examine

A

the effects of more than one IV (called factors) simultaneously.

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14
Q

what is the thing that can be a factor?

A

Essentially anything that can be discretely identified can be a factor (dose, time, type of treatment

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15
Q

Repeated Measures Design (within subjects design)

A

The same test is performed multiple times on the same subject

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16
Q

Repeated Measures Design required

A

Special statistical analyses

the data is no longer completely random.

17
Q

Randomized blocks designs

A

Similar to completely randomized designs except that blocks of subjects are generated or self-select, and then the blocks are assigned randomly across the factors

18
Q

block

A

group of experimental units are similar ,

19
Q

bock are important in

A

decrease the variability within each group , which allows us to detect differences caused by the treatments more clearly

20
Q

types of experimental designs

A

completely randomized design, randomized block design , matched pairs design

21
Q

a stratified, randomized block design

A

If there is an inherent level involved in the randomized block design

22
Q

Matched Samples design.

A

A special case of repeated measures where two different groups are pre-matched to be as identical as possible.

23
Q

This pre-matching introduces

A

a bias and is therefore treated statistically as a special case of repeated measures

24
Q

advantage of Repeated measures

A

reduces within subjects variability
thereby increasing precision and power
leading to a reduction in the number of subjects.

25
Q

Three major disadvantages of repeated measures

A

1- practice effects (only the first test is immune).
2- Differential carry over effects. Prior exposure affects subject in second exposure one way and a different way under another condition.
3- Statistical issues often assume total independence to meet the criteria of randomness (the basic probability o which al stats are based). Since they are repeated measures, randomness is impossible

26
Q

practice effects overcome

A

This problem is overcome by counterbalancing. Practice effects affect all treatment conditions equally.

27
Q

Repeated measures cross over design/two period two treatment design

A

Repeated measures designs are threatened by
carry-over effects, practice effects, and priming.
There is often a washout period (especially true with drug studies).

28
Q

multiple blocks of experimental units and worried about sequence or carry over effects that could threaten the design

A

. You can randomize blocks,

or alternatively using a Latin Square.