Experimental Design

📊Experimental Design Unit 11 – Designing Experiments for Analysis

Designing experiments for analysis is a crucial skill in scientific research. It involves planning studies that test hypotheses and draw valid conclusions. Key concepts include independent and dependent variables, control groups, randomization, and replication. Effective experimental design requires careful consideration of sampling methods, variable control, and data collection strategies. Researchers must also select appropriate statistical analyses and address ethical concerns to ensure their studies are both scientifically rigorous and responsible.

Key Concepts and Terminology

  • Experimental design involves planning and conducting experiments to test hypotheses and draw conclusions
  • Independent variable (IV) represents the factor being manipulated or changed in an experiment
  • Dependent variable (DV) represents the outcome or response being measured in an experiment
  • Extraneous variables are factors that may influence the DV but are not of primary interest in the study
    • Confounding variables are extraneous variables that systematically vary with the IV and can affect the DV
  • Control group serves as a baseline for comparison, typically not exposed to the IV
  • Experimental group is exposed to the IV being tested
  • Randomization involves randomly assigning participants to different groups or conditions to minimize bias
  • Replication refers to repeating an experiment multiple times to assess the consistency of results

Experimental Design Principles

  • Randomization helps ensure that any differences between groups are due to the IV rather than preexisting differences
  • Replication allows researchers to assess the reliability and generalizability of findings
  • Control of extraneous variables is crucial to minimize their influence on the DV
    • Techniques include holding extraneous variables constant, counterbalancing, and using matched pairs
  • Blinding involves keeping participants and/or researchers unaware of the group assignments to reduce bias
    • Single-blind design conceals group assignments from participants
    • Double-blind design conceals group assignments from both participants and researchers
  • Manipulation of the IV should be carefully planned and executed to ensure it is the only factor varying between groups
  • Measurement of the DV should be reliable, valid, and sensitive to changes caused by the IV
  • Sample size should be sufficient to detect meaningful differences between groups and ensure adequate statistical power

Types of Experimental Designs

  • Between-subjects design compares different groups of participants, each exposed to a different level of the IV
  • Within-subjects design exposes each participant to all levels of the IV, allowing for comparisons within individuals
  • Factorial design manipulates two or more IVs simultaneously to examine their individual and combined effects on the DV
    • Allows for the investigation of main effects and interactions between IVs
  • Repeated measures design involves measuring the DV multiple times for each participant under different conditions
  • Quasi-experimental design lacks random assignment of participants to groups but still manipulates the IV
    • Useful when random assignment is not feasible or ethical
  • Single-case design focuses on the detailed analysis of a small number of individuals or cases over time
  • Crossover design exposes each participant to all levels of the IV in a randomized order, with a washout period between conditions

Sampling Methods and Techniques

  • Random sampling involves selecting participants from a population in a way that gives each individual an equal chance of being chosen
    • Helps ensure the sample is representative of the population
  • Stratified sampling divides the population into subgroups (strata) based on specific characteristics and then randomly samples from each stratum
    • Ensures proportional representation of subgroups in the sample
  • Cluster sampling involves dividing the population into clusters (naturally occurring groups) and randomly selecting entire clusters to include in the sample
  • Convenience sampling selects participants based on their availability and willingness to participate
    • May limit the generalizability of findings to the broader population
  • Purposive sampling selects participants based on specific criteria or characteristics relevant to the research question
  • Sample size determination should consider the desired level of statistical power, effect size, and significance level
  • Inclusion and exclusion criteria specify the characteristics that participants must or must not possess to be eligible for the study

Variables and Controls

  • Independent variable (IV) is the factor being manipulated or changed by the researcher
    • Levels of the IV represent the different conditions or groups being compared
  • Dependent variable (DV) is the outcome or response being measured, expected to be influenced by the IV
  • Extraneous variables are factors other than the IV that may affect the DV
    • Control techniques aim to minimize their influence on the DV
  • Control group serves as a baseline for comparison, not exposed to the IV
    • Helps determine if changes in the DV are due to the IV or other factors
  • Placebo control involves giving a fake treatment to the control group to account for placebo effects
  • Positive control is a group exposed to a treatment known to produce the expected effect, used to validate the experimental procedure
  • Manipulation check assesses whether the IV was successfully manipulated as intended
  • Operational definitions specify how variables will be measured or manipulated in the study

Data Collection Strategies

  • Observations involve systematically watching and recording behavior or events
    • Can be structured (using predefined categories) or unstructured (open-ended)
  • Surveys and questionnaires collect self-reported data from participants using a set of questions
    • Can be administered in person, by mail, phone, or online
  • Interviews involve asking participants questions in a one-on-one or group setting
    • Can be structured (fixed questions), semi-structured (mix of fixed and open-ended questions), or unstructured (open-ended)
  • Physiological measures assess biological or physical responses (heart rate, brain activity)
  • Behavioral measures assess overt actions or responses (reaction time, accuracy)
  • Archival data involves using existing records or data sources (medical records, public databases)
  • Triangulation involves using multiple data collection methods to cross-validate findings
  • Pilot testing helps refine data collection procedures and identify potential issues before the main study

Statistical Analysis Approaches

  • Descriptive statistics summarize and describe the main features of a dataset (mean, median, standard deviation)
  • Inferential statistics use sample data to make inferences or draw conclusions about the population
    • Hypothesis testing involves comparing sample data to a null hypothesis to determine if the results are statistically significant
  • t-tests compare means between two groups or conditions
    • Independent samples t-test compares means from two separate groups
    • Paired samples t-test compares means from the same group under two different conditions
  • Analysis of Variance (ANOVA) compares means across three or more groups or conditions
    • One-way ANOVA examines the effect of one IV on the DV
    • Factorial ANOVA examines the effects of two or more IVs on the DV
  • Correlation assesses the strength and direction of the relationship between two variables
  • Regression predicts the value of a DV based on one or more IVs
    • Linear regression assumes a linear relationship between variables
    • Multiple regression includes two or more predictor variables
  • Effect size measures the magnitude of the difference between groups or the strength of the relationship between variables
  • Statistical power is the probability of detecting a true effect when it exists, influenced by sample size, effect size, and significance level

Ethical Considerations in Experimentation

  • Informed consent ensures that participants are fully informed about the study and voluntarily agree to participate
    • Includes information about the purpose, procedures, risks, benefits, and confidentiality of the study
  • Confidentiality protects participants' personal information and ensures that data is kept secure and anonymous
  • Debriefing involves providing participants with additional information about the study after their participation
    • Helps address any concerns or misconceptions and provides resources if needed
  • Minimizing harm and maximizing benefits involves weighing the potential risks and benefits of the study for participants and society
  • Deception should be used sparingly and only when necessary for the integrity of the study
    • Participants must be debriefed and any deception explained
  • Vulnerable populations (children, prisoners, individuals with mental illness) require special considerations and protections
  • Institutional Review Boards (IRBs) review and approve research proposals to ensure they meet ethical standards
  • Responsible conduct of research involves adhering to ethical principles throughout the research process, from planning to dissemination of findings


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© 2024 Fiveable Inc. All rights reserved.
AP® and SAT® are trademarks registered by the College Board, which is not affiliated with, and does not endorse this website.