Nov. 19th - Chapter 10: Research Designs for Special Circumstances Flashcards
3 steps to identifying a causal relationship:
- Temporal precedence (cause comes first - if A causes B, then A MUST come before B)
- Covariation of the cause and effect
* Presence of a cause = presence of effect
* Absence of a cause = absence of effect - Eliminate plausible alternative explanations
Key features of true experiments that help achieve internal validity
- Manipulated Independent Variable(s)
* At least two levels to enable comparison - Measured Dependent Variable(s)
- Experimental control over extraneous variables
* No confounds
* Random assignment to conditions of IV
What is the next best thing when a true experiment isn’t possible?
- Single-case
- Quasi-experiment
- Developmental designs
Single Case - Types:
- ABA Reversal design
* A = baseline
* B = treatment - ABAB Reversal design
- Multiple baseline design (spanning baseline/treatment over multiple days)
Single Case Studies - when you return back to baseline, what is this called?
Reversal design
Single Case Studies: Additional Points
- A few Ps (not a large sample)
- Baseline-treatment: Might add another baseline after, if ethical/possible
- Key feature: Stagger start of treatment; Avoid ‘history’ confound: maybe other events cause a change!
- Does everyone change behavior after treatment?
- Useful to generalize beyond single P
In what areas can multiple baseline measure the effects of the IV?
- Across participants
- Across behaviours (does it control for something else? like dog barks?)
- Across situations (changing environments - home vs. work)
Quasi-Experiments:
What is it?
An attempt to get at causation when you can’t use full experimental design
* Still attempt at IV -> DV
* Just quite a bit messier!!!
Quasi- versus True Experiments
True experiment
* Experimental manipulation
* Random assignment
* Experimental control
Quasi-experiment
* Often no direct manipulation
* No random assignment
* Limited control
In what situation would you choose a quasi-experiment?
Want to study effect of IV on DV, BUT
* Can’t manipulate or control variables
* Can’t use random assignment
- Ethically unfeasible
- Practically unfeasible
Quasi-Experiment Differences: Expanded
- Often no direct manipulation
- No random assignment:
- Subjects are selected based on the values of the independent variable, rather than having the experimenter assign values of the independent variable to subjects (EX: through groups)
- Limited control:
- Quasi-experiments have less internal validity than experiments
- A (poor) quasi-experimental design option Really tells you NOTHING!!!!
Threats to Internal Validity
History
- Something happens in the world at the same time as the onset of treatment & therefore could have caused the effect
- What if other events cause a change?
Threats to Internal Validity
Maturation
- Ps change between pretest and posttest for some reason other than your treatment
- What if the participants just changed on their own?
Threats to Internal Validity
Testing
- Taking the pretest changes responses on posttest (order effects)
- What if the process of testing changed participants?
Threats to Internal Validity
Instrument Decay
- Over repeated use, treatments or measures change, making it look like your treatment had an effect
- What if the measurement instrument changes?
Threats to Internal Validity
How do reduce threats to internal validity:
- Who could you recruit to the comparison group?
- Still no random assignment
- Remember lower internal validity than a true experiment
Types of Quasi-Experiments:
- One-group posttest only
- One-group pretest-posttest
- Nonequivalent control group
- Nonequivalent control group pretest-postest
Multiple Repeated Measures:
* Interrupted time series
Types of Quasi-Experiments:
Nonequivalent control group
- Posttest-only design: still have threats to internal validity = types of alternative explanations
- One being regression toward the Mean
- Extreme scores tend to be less extreme with repeated measures.
Developmental Research
Key Terms: Age Effects
- Age effects: any differences caused by underlying processes, such as biological or psychological changes that occur with aging.
Developmental Research
Key Terms: Cohort Effects
- Cohort effects: Differences caused by experiences and circumstances unique to the generation/cohort to which one belongs
- EX: generations living through WWII versus gen Z
Developmental Research
Key Terms: Time of Measurement Effects
- Time of measurement effects: differences stemming from sociocultural, environmental, historical, or other events at the time of data collection
- Effects are often confounded!
Cross-sectional Design vs. Longitudinal Design
- Compare groups of p’s of differing ages at a single point in time
VERSUS - Observe one group of p’s repeately over time
Cross-sectional - Benefits/Negatives
Benefits:
* COST: Less expensive and immediately yields results
Negatives:
* Must infer developmental change (problematic!)
* Difference may be due to cohort effects
Longitudinal: Benefits/Negatives
Benefits:
* Evidence for developmental change
Negatives:
* Loss of participants (high attrition)
* Expensive and long!
* Measures, interests change
* Results may not generalize to other cohorts
* Possible time of measurement