Research design Henry Flashcards

1
Q

what si the power of a statistical test?

A

The power of a test is the probability to reject H0 if H1 is true.
In albatross example: Power = probability to correctly conclude from your sample that the mean duration of the trip differs between the 2 treatments (magnet, fake magnet)

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2
Q

To be able to carry out the power analysis in G*Power the following information is required:

A
  • The statistical test you
    are you going to use.
  • The desired significance
    level α (mostly 5%)
    =probability to reject H0 if
    H0 is true
  • The desired Power 1-β
    (often in the range 60-
    80%) = probability to
    reject H0 if H1 is true
  • The sample standard
    deviation of the variable
    (from a pilot study or
    from literature)
  • The desired change to be
    detected by the statistical
    test with the desired
    Power
  • If you test one- of two
    sided
  • Allocation ratio (n2/n1
    =sample size group
    magnet /sample size
    group fake magnet)
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3
Q

A true experiment is when:

A
  • There is a control group
  • Animals are randomly
    assigned to the
    treatment or control
    group (each animal has t
    he same chance of
    receiving any one
    treatment)
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4
Q

research design:

A

de wijze waarop de experimentele eenheden (vaak dieren) gerangschikt zijn m.b.t. de behandelingen en de mogelijke storende invloeden.

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5
Q

Experimental design can be split into two categories:

A
  1. Between subject designs
  2. Within-subject designs
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6
Q

Within-subject designs:

A
  • Each experimental unit
    undergoes all the
    treatments
  • Between-subject variation
    is negligible because each
    animal functions as its
    own control
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7
Q

between-subject designs

A
  • Each experimental unit
    undergoes one treatment
  • All animals receive the
    treatment at the same
    time – time-effects are
    negligible
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8
Q

voordelen between-subject designs

A
  • It’s a simple research
    design
  • The statistical tests to be
    used are simple and can
    also be used when the
    number of animals per
    group is not equal
    (Albatross example)
  • Every animal is only
    treated once, resulting in
    a “short” experiment:
    the animal suffers less
    smaller chance that an
    animal must be removed
    from the experiment
    prematurely
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9
Q

nadeel between-subject designs

A

Each treatment is applied to a different set of animals. So, differences between the two treatments can also be due to other factors than the treatment itself because of between-subject variations (e.g. age or sex).

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10
Q

block factor

A

A block-factor is a factor in which we have no interest in but which we take into consideration in the research design because it influences the dependent variable. Its a factor that is measured at the nominal or ordinal level

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11
Q

covariate

A

A covariate is a factor in which we have no interest in but which we take into consideration in the research design because it influences the dependent variable. Its a factor that is measured at the ratio or interval level

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12
Q

voordelen within-subject designs:

A
  • Er wordt niet
    gecorrigeerd voor
    tijdseffecten, er loopt
    namelijk geen
    controlegroep mee
    gedurende de hele proef.
    (zie 10.3.1)
  • Behandelingseffect moet
    reversibel zijn (dat wil
    zeggen dat het dier
    terugkeert naar de
    toestand die hij had voor
    de behandeling ) en het
    dier mag niet gedood
    worden
  • Er wordt dus niet
    gecorrigeerd voor
    zogenaamde carry-over
    effecten (zie 10.3.2)
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13
Q

voordelen within-subject designs

A

Controle voor diereffecten; minder dieren nodig (hogere power)

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14
Q

wat betekent counter-balancing?

A

Er wordt gecorrigeerd voor tijdseffecten omdat elke behandeling in elke periode wordt gegeven.

Door de volgorde van taken te balanceren (bijvoorbeeld sommige deelnemers beginnen met taak A en andere met taak B).

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15
Q

carry-over effect

A

occur when a treatment contineus to affect the subsequent state of experimental subjects.

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16
Q

washout period

A

A period of normal conditions between the two treatments, to minimize carry-over effects.

17
Q

Factoriele schema’s:

A

worden gebruikt als je meerdere behandelingen tegelijk wil testen. Een dier krijgt dus twee of meer behandelingen tegelijkertijd.