Kin 232 Module 5 Flashcards

1
Q

Quasi experimental design

A

Involves manipulation of an independent variable but does not contain a control group and/or randomization

Used under conditions where true experimental designs are not possible or too expensive

Cannot be used to infer causation as conclusively as true experimental trials

Poorer internal validity

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2
Q

Quasi experimental most useful if

A

Control is exerted where possible

Masking procedures are used to solidify design

When preexisting groups exists

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3
Q

If there is no randomization in quasi experimental

A

Use pretest to ensure some level of group equivalent

When there is only a control group: there are two independent variables: time and supplementation

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4
Q

If there is no control group or randomization in quasi experimental

A

Don’t know what could have caused outcome (poor internal validity)

Used when its ethical

When time frame is really short (pilot study)

Independent variable will now be time (there are 2 levels)

The intervention may be initially be considered a indpendent variable but now its not because theres only one level of it, even though it is a “treatment”

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5
Q

Weakness to quasi experimental

A

Groups may not be equivalent , however there is a pretest

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6
Q

Repeated measures in quasi experimental

A

Missing randomization but there still can be many observation periods

Includes prepost , interim assessments, follow up assessments

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7
Q

What threats to internal validity does incorporation of a control group help rule out

A

History, testing, Instrumentation

Better internal validity

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8
Q

Time series Design

A

type of Observation design

Multiple measures to document patterns or trends in behavior over time

Purpose is to determine trend in outcome over time

To make it a quasi experimental design;
Manipulate variables, control group

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9
Q

Interrupted Time Series Design

A

Quasi experimental

Interrupted time series : time series is interrupted by an intervention within the series of measurements

Used for population level interventions (including policy changes)

Randomization not generally possible thus quasi experimental

May or may not have control group

Common in federation level (implication of programs in schools etc)

Repeated measures before and after intervention

A control group can be incorporated

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10
Q

Advantages to Interrupted Time Series Design

A

Time series: multiple measurements enhance confidence that there was a real change versus normal variation / repeated text effects

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11
Q

Disadvantages to Interrupted Time series Design

A

Lack of randomization and/or control still reduced internal validity relative to experimental design

May be a confounding event that occurred at same time as intervention

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12
Q

Exploratory stage in clinical trials phase

A

Preclinical research (cell culture, animals)

Non humans in laboratory conditions

Screens many potential compounds

If promising, request to to human trials

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13
Q

Pre approval stage in clinical trials phases

A

Phase 0 trial
Phase I trial
Phase II trial
Phase III trial

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14
Q

Post approval stage in clinical trials phases

A

Phase IV Trial
Alternate populations

Risk factors, benefits, optimal use

For treatments for cancer

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15
Q

Phase 0 trial

A

First trial in humans

Very small number of healthy people

Very small dose to ensure safety

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16
Q

Phase I trial

A

Determines the largest dose without serious side effects

Larger sample of healthy adults, but still relatively small

Dosage, timing, side-effects

17
Q

Phase II trial

A

Given dose found to be most beneficial in Phase I

Small sample of people with disease / at risk for disease

Effect should be standard treatment to continue trials

For treatments for cancer

18
Q

Phase III trial

A

Randomized controlled trail (masked/blinded)

Large studies with thousands of participants – years

New therapy vs. Standard treatment/placebo