Quantitative Analysis I — Statistics
Session at a Glance
Descriptive and inferential statistics; the logic of hypothesis testing (null, alternative, p-values, Type I/II error); t-tests, one-way ANOVA, correlation; assumption testing; choosing the right test
Hands-on statistical analysis using SPSS, R, or Python — descriptive statistics, t-tests, ANOVA, correlation on real datasets; assumption checking; reporting results in APA format
2 hrs Lecture + 12 hrs Lab/Project
Complete descriptive & basic inferential analysis on pilot or secondary data
Learning Objectives
By the end of this session, you will be able to:
- Compute and interpret descriptive statistics — measures of central tendency, dispersion, and distribution shape — and select the appropriate summary statistics for different variable types and distributions
- Explain the logic of null hypothesis significance testing — including p-values, Type I and Type II error, statistical power, effect size, and confidence intervals — and apply this logic to draw appropriate conclusions from statistical output
- Select, run, and interpret the correct statistical test — independent and paired t-tests, one-way ANOVA with post-hoc comparisons, and Pearson/Spearman correlation — based on research question, variable types, and data structure
- Check and report the assumptions underlying parametric tests — normality, homogeneity of variance, independence — and choose appropriate non-parametric alternatives when assumptions are violated
- Report statistical results in APA 7th edition format, including test statistics, degrees of freedom, p-values, effect sizes, and confidence intervals, with interpretations that connect back to the research questions
Session Planner
Suggested breakdown of the 4-hour contact session.
| Time | Segment | Activity | Mode |
|---|---|---|---|
| 0:00–0:08 | Opening | Recap Unit 2; transition: "You've designed your methodology. Now: when the data comes in, what do you actually DO with it?" The analysis plan from your methodology chapter becomes real this week. | Whole class |
| 0:08–0:30 | Lecture 1 | Descriptive statistics — types of variables, central tendency, dispersion, shape; data screening and cleaning; the logic of inference — populations, samples, sampling distributions, the Central Limit Theorem | Lecture |
| 0:30–0:55 | Lecture 2 | Hypothesis testing framework — null and alternative hypotheses, p-values, Type I/II error, power, effect size, confidence intervals. t-tests: one-sample, independent, paired — when to use each, assumptions, interpretation | Lecture |
| 0:55–1:15 | Activity | Test selection exercise: given 10 research scenarios with variable types and RQs, select the appropriate statistical test. Justify the choice. Identify what the null hypothesis would be. | Pairs |
| 1:15–1:25 | Discussion | Debrief test selection; address common mismatches (e.g., using correlation when a t-test is appropriate, ignoring the independence assumption) | Whole class |
| 1:25–1:40 | Break | — | — |
| 1:40–2:05 | Lecture 3 | One-way ANOVA — between-groups vs within-groups, the F-ratio, post-hoc tests (Tukey, Bonferroni), effect size (eta-squared). Correlation — Pearson vs Spearman, interpreting r and r², correlation matrix reporting. Assumption testing for all parametric tests. | Lecture |
| 2:05–2:20 | Software Demo | Live demonstration: run a complete analysis in SPSS/R/Python — import data, screen for errors, check assumptions, run t-test and ANOVA, interpret output, report in APA format. Students follow along on their own machines. | Demo |
| 2:20–3:50 | Lab Work | Part A: Descriptive statistics and data screening; Part B: t-tests and ANOVA on provided datasets; Part C: Apply analyses to your own pilot or secondary data | Individual |
| 3:50–4:00 | Exit Ticket | Submit analysis output and interpretation; identify the test you are least confident about applying correctly | Individual |
1. Descriptive Statistics — Knowing Your Data Before You Test It
Descriptive statistics are the foundation of all quantitative analysis. Before you test hypotheses, before you run regressions, before you draw any inferential conclusions, you must know your data — its central tendencies, its spread, its shape, its outliers, its missing values. Skipping descriptive statistics is like driving without looking at the dashboard: you may be moving, but you have no idea what is happening under the hood.
Descriptive statistics summarise and describe the main features of a dataset. They answer: what is typical? how much do observations vary? what is the shape of the distribution? are there unusual observations? Descriptive statistics do not test hypotheses or draw conclusions beyond the data at hand — they describe what IS in your sample, not what might be true in the population. That is the job of inferential statistics (Section 2).
1.1 Types of Variables — Your Choice Determines Your Analysis
| Variable Type | Definition | Examples | Appropriate Descriptive Statistics | Appropriate Graphs |
|---|---|---|---|---|
| Nominal (Categorical) | Categories with no inherent order — labels, not quantities | Gender (Male/Female/Other), Industry (IT/Manufacturing/Finance), City, Operating System | Frequency, mode, percentage; no mean or median (meaningless) | Bar chart, pie chart (limited use) |
| Ordinal | Categories with a meaningful order but unknown/unequal distances between categories | Education level, Likert-scale items (individual items, not scale totals), satisfaction ratings, socioeconomic status | Median, mode, frequency, interquartile range; mean is debatable (common in practice but technically assumes equal intervals) | Bar chart, stacked bar |
| Interval / Ratio (Continuous) | Numerical values with equal intervals; ratio variables additionally have a meaningful zero | Age, income, temperature (interval), height, weight, response time, test score, number of purchases (ratio) | Mean, median, mode, standard deviation, variance, range, skewness, kurtosis | Histogram, box plot, density plot, scatter plot |
1.2 The Descriptive Statistics Checklist — What to Report
| Statistic | What It Tells You | When to Use | How to Report (APA) |
|---|---|---|---|
| N (sample size) | How many observations you actually analysed (after handling missing data and exclusions) | Always — for every variable and every subgroup. The reader must know the sample size for every analysis | "The final sample comprised 187 respondents (94 female, 91 male, 2 non-binary)." |
| Mean (M) | The arithmetic average — the centre of the data | For continuous, approximately symmetric variables. Not appropriate for ordinal data (use median) or when there are extreme outliers | "The mean job satisfaction score was 3.72 (SD = 0.84) on a 5-point scale." |
| Median (Mdn) | The middle value — the 50th percentile | For continuous variables with skewed distributions, ordinal variables, or when you need a robust measure of central tendency | "The median response time was 245 ms (IQR = 180–320)." |
| Standard Deviation (SD) | The average distance of observations from the mean — how spread out the data are | For continuous, approximately normal variables reported alongside the mean. The SD is in the original units of the variable | "Participants' ages ranged from 22 to 58 years (M = 34.2, SD = 8.7)." |
| Interquartile Range (IQR) | The range of the middle 50% of observations (Q1 to Q3) — robust to outliers | When the distribution is skewed or you are reporting the median. Report as Q1–Q3 | "The median monthly income was ₹ 45,000 (IQR = ₹ 28,000–75,000)." |
| Minimum / Maximum | The range boundaries — the smallest and largest observed values | Useful for data screening (identifying impossible values) and for providing context. Report with caution if outliers are present | Report in a table or as part of the text: "Scores ranged from 12 to 48." |
| Skewness & Kurtosis | Skewness: asymmetry of the distribution. Kurtosis: the heaviness of the tails (peakedness) | To check the normality assumption for parametric tests. Values between −2 and +2 are generally acceptable for most tests | "The distribution was approximately normal (skewness = −0.34, SE = 0.18; kurtosis = 0.21, SE = 0.35)." |
| Frequencies / Percentages | Counts and proportions for categorical variables | For nominal and ordinal variables. Report both N and % for each category | "Of the 200 respondents, 128 (64%) were from Tier-1 cities, 52 (26%) from Tier-2, and 20 (10%) from Tier-3." |
1.3 Data Screening — The Most Important Step Students Skip
Before running a single inferential test, you must screen your data. Data screening catches errors that, if undetected, produce invalid results. The screening process is not glamorous, but it is what separates competent quantitative researchers from students who get numbers from software and assume they are correct.
- Check for impossible values: Age = 250. Likert response = 7 on a 1–5 scale. Negative reaction time. These are data entry errors. Scan minimum and maximum values for every variable.
- Check for missing data: How much missing data is there? Is it random (MCAR), related to observed variables (MAR), or related to unobserved variables (MNAR)? For capstone purposes: report the percentage of missing data for each variable. If >5% missing, justify your handling approach (listwise deletion, pairwise deletion, mean imputation, or multiple imputation). Never silently delete rows with missing data.
- Check for outliers: Univariate outliers: values more than 3 SD from the mean, or outside 1.5 × IQR on a box plot. Multivariate outliers: unusual combinations of values across multiple variables. For each outlier, decide: is it an error (fix or remove), a genuine extreme value (retain but note), or an influential case (run analysis with and without it to check)?
- Check distributions: Are continuous variables approximately normal? Check histograms, Q-Q plots, skewness/kurtosis values, and Shapiro-Wilk test. This determines whether you can use parametric tests (Section 2) or need non-parametric alternatives.
- Check for duplicates: Are there duplicate rows? (e.g., the same participant submitted the survey twice). Check for duplicate IDs, identical response patterns, or suspiciously fast completion times.
2. Inferential Statistics — The Logic of Drawing Conclusions
Inferential statistics enable you to draw conclusions about a population based on data from a sample. The logic is counterfactual and probabilistic: we ask "if nothing were really going on (the null hypothesis), how likely is it that we would observe data like ours purely by chance?" If that probability is very low, we infer that something probably IS going on. This is the logic of null hypothesis significance testing (NHST).
2.1 The NHST Framework
Null Hypothesis (H0): There is no effect, no difference, no relationship in the population. Any observed pattern in the sample is due to sampling error. Alternative Hypothesis (H1): There IS an effect, difference, or relationship in the population. Example: H0: μtreatment = μcontrol (the means are equal). H1: μtreatment ≠ μcontrol (the means differ).
Alpha is your threshold for statistical significance — the probability of a Type I error you are willing to accept. Convention: α = 0.05. This means: if the null is true, there is a 5% chance of incorrectly rejecting it. Important: α = 0.05 is a convention, not a law. It means "we accept a 1-in-20 false positive rate." In some contexts (medical trials), α = 0.01 is used. In exploratory research, α = 0.10 may be acceptable. Justify your choice.
The test statistic (t, F, r, χ²) quantifies the strength of evidence against the null. It is the ratio: (observed effect) / (expected random variation). A large test statistic means the observed effect is large relative to what we would expect by chance alone. The formula depends on the test, but the logic is the same: signal divided by noise.
The p-value is: the probability of observing data at least as extreme as yours, IF the null hypothesis is true. It is NOT the probability that the null is true. It is NOT the probability that your results are due to chance. It is a conditional probability: P(data | H0). A small p-value says: "If the null were true, my data would be very surprising." This leads us to doubt the null.
If p ≤ α: Reject H0. The result is "statistically significant." Conclude that there IS evidence of an effect/difference/relationship. If p > α: Fail to reject H0. The result is "not statistically significant." Conclude that there is INSUFFICIENT evidence of an effect. You do NOT conclude "there is no effect" — you conclude "the data do not provide sufficient evidence to conclude there is an effect."
Statistical significance tells you WHETHER an effect exists (given your α threshold). Effect size tells you HOW LARGE the effect is — its practical significance. A statistically significant result with a tiny effect size may be meaningless in practice. Confidence intervals tell you the precision of your estimate. Always report effect size and CI alongside p-values.
2.2 Type I and Type II Error — The Two Ways to Be Wrong
| H0 is TRUE (no effect) | H0 is FALSE (real effect) | |
|---|---|---|
| Reject H0 (significant) | Type I Error (α) False positive — concluding there is an effect when there isn't one. Probability = α (typically .05) | Correct Decision (Power = 1−β) True positive — correctly detecting a real effect. Probability depends on effect size, sample size, and α |
| Fail to Reject H0 (non-significant) | Correct Decision (1−α) True negative — correctly not claiming an effect when none exists. Probability = .95 when α = .05 | Type II Error (β) False negative — failing to detect a real effect. Most commonly caused by insufficient sample size (low power) |
The .05 threshold is the most widely misunderstood concept in quantitative research. Common errors to avoid: (1) "p = .051 is non-significant, so there is no effect. p = .049 is significant, so there IS an effect." — the difference between .049 and .051 is meaningless; both are continuous evidence, not binary categories. (2) "p < .001 means the effect is very large." — p-values depend on sample size; with a large enough sample, even trivially small effects become "highly significant." (3) "The result was non-significant, so the null hypothesis is true." — absence of evidence is not evidence of absence. A non-significant result may mean no effect OR insufficient power to detect an effect. (4) "The p-value is the probability that my results are due to chance." — The p-value assumes the null is true; it cannot tell you the probability that the null is true. Report p-values as continuous values (p = .032), not as inequalities (p < .05). Report effect sizes and confidence intervals ALONGSIDE p-values. A finding is the combination of its significance, its magnitude, and its precision — not its p-value alone.
3. t-Tests — Comparing Means
The t-test is the most fundamental inferential test: it compares means to determine whether an observed difference is larger than would be expected by sampling error alone. Despite its simplicity, the t-test is often used incorrectly — applied to the wrong data structure, with violated assumptions, or without the appropriate variant for the research design.
3.1 The Three t-Tests — When to Use Each
| Test | What It Compares | Data Structure | Example RQ | H0 |
|---|---|---|---|---|
| Independent Samples t-test | The means of a continuous DV between TWO independent groups | One categorical IV (2 groups) + one continuous DV. Each participant is in ONE group only. | "Do male and female employees differ in job satisfaction?" (IV: gender, 2 groups; DV: satisfaction score) | H0: μmale = μfemale |
| Paired Samples t-test | The means of a continuous DV at TWO time points (or under two conditions) within the SAME participants | One continuous DV measured twice on the same participants. Each participant provides two data points. | "Does employee satisfaction change from before (pre-test) to after (post-test) a training intervention?" | H0: μdifference = 0 (the mean of the pre-post differences is zero) |
| One-Sample t-test | The mean of a continuous variable against a KNOWN or HYPOTHESISED population value | One continuous variable; a known or hypothesised population mean to compare against | "Is the mean customer satisfaction score in this sample significantly different from the industry benchmark of 3.5?" | H0: μsample = 3.5 (the population mean equals the benchmark) |
3.2 Assumptions of the t-Test
| Assumption | What It Means | How to Check | What to Do If Violated |
|---|---|---|---|
| Independence | Observations are independent of each other — one participant's score does not influence another's. THE most important assumption. | Check the study design. Are participants nested in groups (teams, classes, organisations)? If so, independence may be violated (use multilevel modelling or clustered standard errors). | Use paired test for dependent observations; use multilevel modelling for nested data. If independence is severely violated, standard errors will be wrong and results invalid. |
| Normality | The DV is approximately normally distributed in each group (for independent t-test) or the differences are approximately normal (for paired t-test) | Visual: histogram, Q-Q plot. Statistical: Shapiro-Wilk test. Practical: skewness and kurtosis values. With n ≥ 30 per group, the CLT makes the t-test robust to moderate non-normality. | If severe non-normality (skewness > |2|) and n < 30: use Mann-Whitney U test (independent) or Wilcoxon signed-rank test (paired) — non-parametric alternatives that don't assume normality. |
| Homogeneity of Variance | The variance of the DV is approximately equal across groups (for independent t-test only) | Levene's test. If p > .05, variances are not significantly different — assumption met. If p ≤ .05, variances differ — assumption violated. | Use Welch's t-test (does not assume equal variances). SPSS reports both; the "equal variances not assumed" row is Welch's. This is the safer default when variances differ. |
3.3 Reporting a t-Test in APA Format
Template: "An independent-samples t-test was conducted to compare [DV] between [Group 1] and [Group 2]. There was a [significant / non-significant] difference in scores between [Group 1] (M = [mean], SD = [SD]) and [Group 2] (M = [mean], SD = [SD]); t([df]) = [t-value], p = [p-value], d = [Cohen's d], 95% CI [lower, upper]."
Worked Example: "An independent-samples t-test was conducted to compare job satisfaction between employees with flexible work arrangements and those without. There was a significant difference in satisfaction scores between employees with flexible arrangements (M = 4.12, SD = 0.68, n = 94) and those without (M = 3.47, SD = 0.81, n = 93); t(176.45) = 5.92, p < .001, d = 0.87, 95% CI [0.43, 0.87]. Levene's test was significant (p = .04), so Welch's t-test with adjusted degrees of freedom is reported. The effect size indicates a large practical difference between groups."
4. One-Way ANOVA — Comparing Three or More Means
When you need to compare means across three or more groups, running multiple t-tests inflates the Type I error rate. Three groups require three pairwise comparisons; at α = .05 per test, the familywise error rate is approximately 1 − (0.95)³ = .14 — nearly three times the acceptable rate. ANOVA solves this by testing all group means simultaneously: "are there ANY differences among these groups?"
4.1 The Logic of ANOVA
ANOVA partitions the total variance in the DV into two components: between-groups variance (differences among group means — the effect you are testing) and within-groups variance (differences among individuals within the same group — error). The F-ratio is: F = (between-groups variance) / (within-groups variance). If the group means differ substantially (large between-groups variance) relative to the natural variation within groups (small within-groups variance), F will be large, and the result will be significant.
A significant omnibus F-test tells you that at least one group mean differs from the others — but it does NOT tell you WHICH groups differ. To determine which specific pairs of groups differ, you must conduct post-hoc tests (e.g., Tukey's HSD, Bonferroni). Post-hoc tests control the familywise error rate across all pairwise comparisons — unlike running multiple t-tests with no correction. A common student error: reporting a significant F-test and then describing which groups "look different" based on the means, without conducting post-hoc tests. This is not acceptable — the visual difference may not be statistically significant.
4.2 One-Way ANOVA — Between-Groups
| Element | Description |
|---|---|
| When to Use | One categorical IV with 3+ independent groups; one continuous DV. Example: comparing employee satisfaction across four departments (IT, Marketing, Finance, HR). |
| Assumptions | Same as independent t-test: independence, normality (within each group), homogeneity of variance (Levene's test). |
| Key Output | F(dfbetween, dfwithin) = F-value, p-value, η² (eta-squared: proportion of variance in DV explained by the IV). |
| Post-Hoc Tests | Tukey's HSD: Most common; controls familywise error; compares all pairwise means. Use when group sizes are equal or approximately equal. Bonferroni: More conservative (lower power); divides α by number of comparisons. Use when you have specific planned comparisons. Games-Howell: Use when the homogeneity of variance assumption is violated (does not assume equal variances). |
| APA Report | "A one-way between-groups ANOVA was conducted to compare the effect of [IV] on [DV]. There was a significant effect of [IV] on [DV] at the p < .05 level: F([dfbetween], [dfwithin]) = [F], p = [p], η² = [value]. Post-hoc comparisons using Tukey's HSD test indicated that the mean score for [Group A] (M = [mean], SD = [SD]) was significantly different from [Group B] (M = [mean], SD = [SD]), p = [p]. No other comparisons were significant." |
4.3 Non-Parametric Alternatives
| Parametric Test | Non-Parametric Alternative | When to Use the Alternative |
|---|---|---|
| Independent t-test | Mann-Whitney U test (Wilcoxon rank-sum) | Severe non-normality with small samples (n < 30 per group); ordinal DV |
| Paired t-test | Wilcoxon Signed-Rank test | Severely non-normal differences with small samples |
| One-way between-groups ANOVA | Kruskal-Wallis H test | Severe non-normality with small n per group; ordinal DV; heterogeneity of variance that Games-Howell cannot address |
5. Correlation — Measuring the Strength of Relationships
Correlation quantifies the strength and direction of the linear relationship between two continuous variables. It is the foundation of regression (Week 14), the basis for reliability analysis (Cronbach's alpha is a form of correlation), and one of the most commonly reported statistics in quantitative capstone research. It is also one of the most commonly misinterpreted: correlation does not imply causation, a point that cannot be stated too frequently.
5.1 Pearson and Spearman Correlation
| Dimension | Pearson Correlation (r) | Spearman Correlation (rs or ρ) |
|---|---|---|
| What It Measures | The strength and direction of the LINEAR relationship between two continuous variables | The strength and direction of the MONOTONIC relationship between two variables (can be used with ordinal data or non-normal continuous data) |
| Range | −1 to +1. −1 = perfect negative linear relationship; 0 = no linear relationship; +1 = perfect positive linear relationship | −1 to +1. Interpreted similarly to Pearson, but based on ranks, not raw values |
| Assumptions | Both variables are continuous, approximately normally distributed, linearly related, with no extreme outliers | Variables are at least ordinal; relationship is monotonic (as one increases, the other consistently increases or decreases, but not necessarily in a straight line) |
| r² — Coefficient of Determination | The proportion of variance in one variable that is shared with (explained by) the other. r = .50 → r² = .25 → 25% shared variance. An apparently "moderate" correlation of .50 actually shares only 25% of variance. | Not directly interpretable as variance explained; Spearman's r² approximates shared variance but is less intuitive than Pearson's |
5.2 Interpreting Correlation Coefficients — Cohen's Guidelines
| |r| | Interpretation | r² | What This Means in Plain Language |
|---|---|---|---|
| .10 | Small / Weak | 1% | The variables share 1% of their variance — knowing one tells you almost nothing about the other. With a large sample, even r = .10 can be statistically significant. It is still a small effect. |
| .30 | Medium / Moderate | 9% | The variables share 9% of their variance. This is a meaningful effect in many social science contexts. Many published correlations in management and psychology are in the .20–.40 range. |
| .50 | Large / Strong | 25% | The variables share 25% of their variance. This is a substantial effect. Three-quarters of the variance is still unexplained — correlation, even "large" ones, leave much unknown. |
5.3 Correlation Matrix — How to Report Multiple Correlations
| Variable | M | SD | 1 | 2 | 3 | 4 |
|---|---|---|---|---|---|---|
| 1. Job Satisfaction | 3.72 | 0.84 | — | |||
| 2. Autonomy | 3.91 | 0.76 | .48** | — | ||
| 3. Work-Life Balance | 3.15 | 0.92 | .52** | .34** | — | |
| 4. Turnover Intention | 2.63 | 1.05 | −.61** | −.29* | −.45** | — |
Note. N = 187. *p < .05. **p < .01. M and SD are on a 1–5 Likert scale.
Key reporting conventions: (1) Report means and SDs in the first columns. (2) The diagonal is dashes (a variable correlates perfectly with itself). (3) Report only the lower or upper triangle — the matrix is symmetric. (4) Use asterisks for significance levels and define them in a note. (5) Always include the sample size (N). (6) If you have 6+ variables, a correlation matrix in a table is more appropriate than listing all pairs in the text.
(1) Correlation = Causation: r = .52 between social media use and anxiety does NOT mean social media causes anxiety. It could mean anxious people use more social media. Or a third variable (sleep quality, loneliness) drives both. Or the relationship is bidirectional. (2) Ignoring r²: r = .30 sounds moderate, but r² = .09 means 91% of variance is unexplained. (3) Ignoring non-linearity: Pearson's r = .00 does not mean "no relationship" — it means "no LINEAR relationship." A perfect U-shaped relationship has r = .00. Always plot your data before computing correlations. (4) Computing correlations on ordinal data: Computing Pearson's r on individual Likert items (1–5 scale) is technically questionable (ordinal data). In practice, it is widely done for scale totals (sum/average of multiple items) which are treated as continuous. For individual ordinal items, use Spearman.
Think Deeper — Cross Questions
Discuss in pairs before sharing with the class.
A researcher conducts a study with n = 1,000 and finds a significant correlation between coffee consumption and job performance: r = .09, p = .004. They conclude: "Coffee consumption significantly improves job performance." Critique every element of this statement. Is r = .09 meaningful regardless of its p-value? What does r² tell you? Can the causal direction be determined? What alternative explanations exist? What should the researcher have concluded instead?
You run an independent t-test comparing the mean productivity scores of employees in open-plan offices (M = 68.2, SD = 14.5, n = 45) and those in private offices (M = 72.8, SD = 13.1, n = 42). The result is: t(85) = −1.52, p = .13. Your supervisor says: "See? Office type doesn't affect productivity." Critique this interpretation. What can you legitimately conclude from p = .13? What additional information would you need before concluding "no effect"? How should you report this result?
A student runs a one-way ANOVA comparing customer satisfaction across three store types: premium (M = 4.41), mid-range (M = 4.12), and discount (M = 3.88). The omnibus F-test is significant: F(2, 147) = 4.37, p = .014. The student reports: "Customer satisfaction was highest in premium stores, followed by mid-range stores, and lowest in discount stores. Therefore, premium stores provide the best customer experience." What is missing from this analysis? What additional statistical step must the student take before making pairwise claims? What if Tukey's HSD reveals that the only significant difference is between premium and discount stores, while the mid-range comparison is non-significant — how does this change the narrative?
A BCA student evaluates their model on two benchmark datasets and wants to compare the F1 scores. Dataset A: M = 0.82, SD = 0.04 (10-fold CV). Dataset B: M = 0.85, SD = 0.03 (10-fold CV). They run an independent t-test: t(18) = −1.90, p = .074. They conclude the models are "not significantly different." Is a t-test appropriate for this comparison? What specific concerns arise when comparing model performance across datasets of potentially different difficulty? What would be a more appropriate analytical approach — and what additional information would you need?
Quick Check — Test Selection
For each research scenario, select the most appropriate statistical test.
1. You want to compare the mean job satisfaction scores of employees across three organisation types: startups, SMEs, and large corporations. Each employee works in only one organisation type.
2. You measure employee engagement before and after a team-building intervention on the same 60 employees. You want to know if engagement changed.
3. You have two continuous variables — hours of training per year and annual performance rating — and you want to know whether there is a linear relationship between them.
4. Your Shapiro-Wilk test is significant (p = .002) for your DV in both groups, and your sample size is n = 18 per group. You need to compare means between two independent groups.
Knowledge Check — Interactive Quiz
Test your understanding of quantitative statistics.
Q1. A p-value of .03 means:
Q2. You run a one-way ANOVA and obtain a significant F-test. What must you do before claiming which specific groups differ?
Q3. When the homogeneity of variance assumption is violated for an independent t-test, what should you do?
Q4. A Pearson correlation of r = −.65 between job stress and job satisfaction means:
Q5. Which of the following is the most robust approach when your continuous DV is severely skewed in a small sample (n < 25 per group) and you need to compare two independent groups?
Lab Activity — Hands-On Statistical Analysis
Part A: Descriptive Statistics and Data Screening (45 min)
- Import your dataset (or use the provided practice dataset) into SPSS, R, or Python.
- Run descriptive statistics for all variables: N, mean, median, SD, min, max, skewness, kurtosis. For categorical variables: frequencies and percentages.
- Screen for problems: Check min/max for impossible values. Identify missing data patterns. Run box plots to identify outliers. Check distributions with histograms and Shapiro-Wilk tests.
- Document every screening decision: For each outlier found, note: (a) is it an error or a genuine value? (b) what did you do with it? For missing data: how much is missing, for which variables, and how will you handle it?
Part B: t-Tests and ANOVA on Practice Data (60 min)
| Analysis | RQ | Assumptions to Check | Key Output | APA Report |
|---|---|---|---|---|
| Independent t-test | Compare DV between two groups | Normality (per group), Levene's test | t, df, p, M per group, SD per group, Cohen's d | |
| Paired t-test | Compare DV at two time points | Normality of difference scores | t, df, p, M pre, M post, SDs, Cohen's d | |
| One-way ANOVA | Compare DV across 3+ groups | Normality (per group), Levene's test | F, df, p, η², post-hoc results | |
| Pearson correlation | Relationship between two continuous variables | Normality, linearity, no extreme outliers | r, p, r² |
Part C: Apply to Your Own Data (45 min)
If you have pilot data, secondary data, or a practice dataset that mirrors your expected capstone data: run the analyses specified in your methodology chapter. If you do not yet have data, use the provided practice datasets. Complete the Analysis Report Table:
| RQ | Test Used | Assumptions Met? | Result (APA format) | Interpretation (1–2 sentences connecting to RQ) |
|---|---|---|---|---|
| Example: RQ1 | Independent t-test | Yes (Levene's p = .34; normality OK) | t(178) = 3.42, p < .001, d = 0.51 | Employees with flexible arrangements reported significantly higher satisfaction than those without. The effect was medium-sized, supporting the hypothesised relationship. |
Exit Ticket
Submit with your analysis output.
- Submit the results of at least one inferential test (t-test, ANOVA, or correlation) with full APA-format reporting and interpretation.
- Did your data meet the assumptions of the test you used? If not, what alternative did you use or what corrective action did you take?
- Looking at your methodology chapter's analysis plan: Which test specified in your plan are you least confident about running correctly, and why?
- If you have your own data: What did data screening reveal — any outliers, missing patterns, or distribution issues? If you used practice data: What would you do differently when screening your actual capstone data?
- One question about statistics that you still find confusing:
Key Takeaways — Week 13
Data screening is not optional. Impossible values, missing data, outliers, and non-normal distributions will invalidate your results if undetected. Every analysis should begin with descriptive statistics and assumption checking. Report what you found — including the problems — transparently.
A p-value quantifies evidence against the null — nothing more. Always report effect sizes and confidence intervals alongside p-values. A significant p-value with a tiny effect is meaningless. A non-significant p-value does not prove the null. Treat p-values as continuous evidence, not binary decisions.
The statistical test is determined by your RQ, your variable types, and your data structure — not by what you know how to run. Independent groups require independent tests; repeated measures require paired tests; 3+ groups require ANOVA with post-hoc tests. Choosing the wrong test produces invalid results regardless of how correctly you run it.
Every parametric test has assumptions. Check them. Report them. If violated, either use a non-parametric alternative or justify why the test is robust to the violation in your specific case (with citations). "I assumed the assumptions were met" is not a defensible statement in a methodology or results chapter.
Facilitator Notes
Preparation Checklist
- Prepare 2–3 practice datasets with known properties: one with clear group differences (for t-test/ANOVA), one with clear correlations, and one with deliberate problems (outliers, missing data, non-normal distributions) to teach data screening.
- Prepare step-by-step software guides for SPSS, R, and Python covering: importing data, descriptive statistics, assumption checking, t-tests, ANOVA, correlations, and APA-format reporting. Students will refer to these throughout their capstone.
- Prepare the live demo carefully — test that the dataset works correctly with the software version students have installed. A demo that crashes due to software version mismatches undermines confidence. Have screenshots as backup.
- For the test selection activity, prepare 10 scenario cards with RQs, variable types, and sample sizes. Include: 3 clear independent t-test, 2 paired t-test, 2 one-way ANOVA, 2 correlation, and 1 ambiguous case that could be approached multiple ways.
Common Student Difficulties
- Statistical anxiety: Many BBA and some BCA students have maths anxiety. Normalise this. Emphasise that statistics is a skill learned through practice, not a talent. The software does the computation — the researcher's job is to know which test to use, check assumptions, and interpret output correctly.
- Confusing statistical significance with practical importance: Students see p < .05 and declare victory without looking at effect size. Drill the habit: "What is the effect size? What does it mean in practical terms? Would anyone in the real world care about a difference this small?"
- Running tests without checking assumptions: Students go straight to the p-value. Require the sequence: screen data → check assumptions → run test → report effect size → interpret. Build this as a checklist that must be completed for every analysis.
- Choosing the wrong test for the data structure: Using independent t-tests for repeated measures (ignoring the pairing). Using t-tests for 3+ groups (inflating Type I error). Using Pearson correlation for clearly non-linear relationships. The test selection activity directly targets this.
Pacing Tips
- This week works best when students are on their own machines running analyses as you demonstrate. Allocate extra time for technical troubleshooting — software installation issues, version differences, and operating system quirks will consume time. Have teaching assistants circulating during the lab.
- Not all students will use quantitative methods. Students doing purely qualitative capstones should still understand the logic of NHST (Section 2) — it is part of research literacy. They can spend lab time on qualitative analysis preparation (transcription, coding software setup) rather than t-tests.
- Week 14 (Regression) builds directly on this week's correlation foundation. Ensure students are comfortable with correlation before they leave — regression is correlation extended to multiple predictors with a directional model.