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Foundations of Quantitative Measurement
Variables in clinical psychology research:
Cognitive
Affective
Behavioural
Biological
Social
Construct: Underlying psychological concept.
Measure: Indicator or way of observing a construct.
Operationalization: Process of going from construct to measure.
Construct is latent and inferred from measurement operations.
Converging operations: Using multiple indicators to measure constructs.
Reactivity of measurement: Participants' behavior changes due to being measured.
Measurement Sources and Approaches
Self-report: Attitude questionnaires, symptom checklists.
Observation: Behavioural observation, brain scan.
Qualitative: Qualitative interviews, diaries, journals, participant observation, projective tests.
Advantages of Quantitative Measurement
Greater precision in measurement.
Well-developed theory of reliability and validity.
Established statistical methods for data analysis.
Data can be easily summarized.
Facilitates comparison across individuals.
Fits well with hypothetico-deductive approaches.
Sampling theory can be used to estimate generalizability.
Positivism
Focuses on observable facts.
Applies methods used in physical sciences to social sciences.
Emphasizes objectivity and value-free science.
Logical positivism restricts philosophical discourse to sensory experience.
Methodological Behaviourism
Focuses on observable behaviour.
Excludes inner factors like cognitions and emotions.
Criticisms of Positivism
Excludes psychological constructs related to human experience.
Linked to capitalism, potentially reducing everything to numbers.
Chronometric Methods
Reaction time (RT) increases with task complexity.
Hick-Hyman law: RT is linearly related to information extracted from the stimulus.
Donders’ Method of Subtraction
Reaction times (RT) are crucial for studying the organization of mental processes.
Tasks:
Task A: Simple detection task
Task B: Discrimination task
Task C: Go/no-go task
Assumptions: consecutive cognitive processes are strictly serial and independent of each other.
Additive Factors Logic
Mental processing stages and their organization can be determined from systematic statistical interactions obtained with a single task.
Additive effects indicate different processes; interactions suggest variables affect the same process.
Interpreting Reaction Time Differences
Observed RT effect might be driven by unknown factors.
Control conditions help exclude alternative explanations.
Descriptive Designs
Study phenomena without manipulating variables.
Uses descriptive statistics (percentages, means).
May lead to correlational designs.
Correlational Designs
Find out how variables are related.
Measure many variables for each participant to study relations between them.
Cross-sectional or longitudinal.
Methods: Correlation coefficients, multiple regression, factor analysis, structural equation modelling.
Correlation and Causation
Correlation does not equal causation.
Conditions for inferring causality:
Covariation
Precedence
Exclusion of Alternative Explanations
Logical Mechanism
Conceptualizing causality: Path analysis.
Issues in drawing causal conclusions:
Direct causality
Reverse causality
Spurious relationships
Mediating factors
Moderating factors
Experimental Designs
Manipulate independent variable; use control group.
Establish cause-effect relationships.
Forms: Factorial, repeated-measures.
Statistical techniques: ANOVA, t-tests.
Assess validity to determine the strength of experimental design.
Cook and Campbell’s Validity Analysis
Internal validity: Differences in the dependent variable are caused by the independent variable.
External validity: Results can be generalized to other tests.
Framework encompasses statistical conclusion and construct validity.
Potential weaknesses in research study are flaws and limitations.
Validity Type & Defining Question
Statistical conclusion: Is there an effect?
Internal: Is it causal?
Construct: What does it mean?
External: Does it generalize?
Nonrandomized Designs
One-group Posttest-Only Design (XO): Lacks sufficient evidence for causal inferences.
One-group Pretest-Posttest Design (O1 X O2): Risky for inferring causation.
Nonequivalent Groups Posttest-Only Design (NR X O NR O): Major threat is uncontrolled selection.
Nonequivalent Groups Pretest-Posttest Design (NR O X O NR O (Y) O): Mitigate uncontrolled selection with statistical methods.
Interrupted Time-Series Design (O1 O2 … O20 X O21 … O40): Requires careful monitoring for interfering events.
Randomized Designs
Random assignment eliminates selection bias.
Enables manipulation of a single variable and fulfillment of causality conditions.
Control and comparison groups isolate effects of key variables.
Internal validity is often prioritized over external validity.
Design Variations
Basic Pretest-Posttest Design: ROXO R O (Y) O.
Multiple levels: Adding more experimental or control groups.
Multi-factorial Designs: Incorporating more than one between-groups factor.
Repeated-measures Designs: Assessing the same individuals at multiple points in time.
Blocking Factors: Grouping participants based on individual differences before randomization.
Analysis of Covariance: Individual differences have a linear relationship with the outcome variable.
Ethical considerations and scientific value determine the choice of control group.
Limitations of Randomized Designs
Ethical constraints prevent randomization in studying negative experiences.
RCTs may be unnecessary or inappropriate for obvious interventions.
Design requirements can make RCTs unrepresentative of normal clinical practice.
RCTs do not account for patient choice and may be influenced by researcher allegiance.
Practical issues: Ensuring group equivalence, dealing with attrition, preventing condition leakage, obtaining staff cooperation.
RCTs are costly and time-consuming.
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