Module 24

Statistical Reporting

Communicating results clearly, completely, and honestly

Principles of Good Reporting

  • 01

    Complete Reporting

    Report all analyses, not just significant ones

  • 02

    Effect Sizes

    Always include magnitude, not just p-values

  • 03

    Uncertainty

    Report confidence intervals and precision

  • 04

    Transparency

    Pre-registration, open data, reproducibility

01

APA Statistical Notation

Standard Notation Conventions

StatisticSymbolFormat
MeanMM = 12.45
Standard DeviationSDSD = 3.21
Sample Sizen, Nn = 45 (group), N = 90 (total)
p-valuepp = .023 or p < .001
Correlationrr(48) = .45, p = .001
Cohen's ddd = 0.65

APA style uses italics for statistical symbols, leading zeros only for values that can exceed 1 (so 'p = .05' not 'p = 0.05'), and specific decimal places (usually 2-3). These conventions ensure clarity and consistency.

Reporting t-tests

Complete t-test Report
The treatment group (M = 75.3, SD = 12.4) scored significantly higher than the control group (M = 68.2, SD = 11.8), t(58) = 2.34, p = .023, d = 0.61, 95% CI [0.08, 1.13].
Includes: Descriptives (M, SD) for both groups, test statistic with df, exact p-value, effect size (d), CI for effect size

A complete t-test report includes descriptive statistics for both groups, the t-statistic with degrees of freedom, exact p-value (or < .001), effect size (Cohen's d), and a confidence interval around the effect.

Reporting ANOVA

Complete ANOVA Report
There was a significant main effect of treatment, F(2, 87) = 5.43, p = .006, η2p = .11. Post-hoc comparisons using Tukey's HSD indicated that the high-dose group (M = 23.4, SD = 4.2) differed significantly from placebo (M = 18.6, SD = 4.8), p = .004, but the low-dose group (M = 20.1, SD = 4.5) did not differ from either, ps > .10.
Includes: F-ratio, df (between, within), p, effect size (η²), post-hoc results

ANOVA reports need the F-ratio with both degrees of freedom (between-groups, within-groups), p-value, effect size (eta-squared or partial eta-squared), and post-hoc comparisons when the omnibus test is significant.

Reporting Regression

Complete Regression Report
A multiple regression was conducted to predict salary from years of experience and education level. The model was significant, F(2, 147) = 34.56, p < .001, R2 = .32, adjusted R2 = .31. Years of experience significantly predicted salary, β = .45, t(147) = 5.67, p < .001, as did education, β = .28, t(147) = 3.52, p < .001.
PredictorBSEβtp
Experience2,450432.455.67< .001
Education8,3202,364.283.52< .001

Regression reports should include overall model fit (F, R², adjusted R²), and for each predictor: unstandardized (B) and standardized (β) coefficients, standard errors, t-values, and p-values. Tables are preferred for multiple predictors.

02

Reporting Effect Sizes

Why Effect Sizes Matter

Same p-value, Different Stories
Study 1: n = 30
t(28) = 2.15, p = .040
d = 0.79
Large effect, small sample
Study 2: n = 500
t(498) = 2.15, p = .032
d = 0.19
Tiny effect, large sample
Similar p-values but completely different practical implications! Effect sizes reveal the true story.

P-values depend on both effect size AND sample size. Two studies with similar p-values can have vastly different effect sizes. Always report effect sizes to show the magnitude of your findings, not just their statistical reliability.

Choosing Effect Size Measures

AnalysisEffect SizeSmall/Med/Large
t-testCohen's d0.2 / 0.5 / 0.8
Correlationr (itself is ES).1 / .3 / .5
ANOVAη² or η²ₚ.01 / .06 / .14
RegressionR², f², β.02 / .13 / .26 (R²)
Chi-squareCramér's V, φ.1 / .3 / .5
Non-parametricRank-biserial r.1 / .3 / .5

Different analyses require different effect size measures. Cohen's d for comparing means, r for correlations, eta-squared for ANOVA, R² for regression. Use the appropriate measure and report conventional benchmarks for interpretation.

Confidence Intervals for Effect Sizes

Effect Size with 95% CI
0 (no effect) d = 0.65 [0.21, 1.09]
The CI excludes zero → effect is significant. Width shows precision. Readers can see the range of plausible effect sizes.

Confidence intervals around effect sizes show both significance (if CI excludes zero) and precision. A wide CI means uncertainty about the true effect magnitude. CIs are more informative than p-values alone.

03

Transparency Practices

Pre-registration

What to Pre-register
Hypotheses
Specific, directional predictions
Sample Size
Power analysis, stopping rules
Variables
How measured, which are primary
Analysis Plan
Exact tests, exclusion criteria
Platforms: OSF, AsPredicted, ClinicalTrials.gov

Pre-registration means publicly documenting your hypotheses, methods, and analysis plan BEFORE collecting data. This prevents p-hacking, HARKing (Hypothesizing After Results are Known), and publication bias. It's becoming standard in many fields.

Open Science Practices

📊
Open Data
Share raw, anonymized data on OSF, Zenodo, etc.
💻
Open Code
Share analysis scripts (R, Python) on GitHub
📄
Open Materials
Share stimuli, questionnaires, protocols
🔓
Open Access
Make paper freely available (preprint, gold OA)

Open science makes research more transparent and reproducible. Sharing data allows replication and secondary analysis. Sharing code ensures analyses can be verified. These practices build trust and accelerate science.

Complete Reporting

Report ALL Analyses
🚫 Don't Do This
• Run 20 tests, report only 3 significant ones
• Try multiple DVs, report the best
• Remove outliers until p < .05
✓ Do This
• Report all planned analyses
• Label exploratory analyses as such
• Pre-specify exclusion criteria
Rule: The number of tests run should equal the number reported (for confirmatory analyses)

Selective reporting (only publishing significant results) inflates the false positive rate in the literature. Report all pre-planned analyses, clearly distinguish confirmatory from exploratory, and don't hide null results.

04

Data Visualization

Effective Statistical Graphics

Good Practice
• Show raw data (points, distributions)
• Include error bars (SE or CI)
• Start y-axis at zero (usually)
• Label axes clearly with units
• Use colorblind-friendly palettes
Bad Practice
• Truncated axes to exaggerate effects
• Bar charts hiding distribution shape
• 3D effects that distort perception
• Unlabeled or ambiguous legends
• Pie charts for comparisons

Good visualizations accurately represent data without distortion. Show individual data points when possible, include uncertainty (error bars, CIs), and avoid visual tricks that exaggerate effects. Honesty in graphics matches honesty in statistics.

Show the Data, Not Just Summaries

Bar Chart Only
Hides distribution shape
With Individual Points
Shows raw data + summary

Bar charts with error bars hide crucial information about distributions. Better alternatives include violin plots, box plots with points, or raincloud plots. When sample size permits, show individual data points alongside summaries.

Error Bar Types

TypeShowsUse When
SDData spread (variability in sample)Describing the sample itself
SEPrecision of mean estimateHow precisely we estimated mean
95% CIPlausible range for true meanInference about population
Rule of thumb: 95% CI ≈ 2 × SE. Non-overlapping 95% CIs usually mean p < .05 (but not always!)

Different error bars mean different things! SD shows data spread, SE shows precision of the mean, 95% CI shows where the true population value likely lies. Always specify which you're using - never just say 'error bars.'

05

Common Reporting Issues

The p < .05 Problem

Result A
p = .049
"Significant!"
Result B
p = .051
"Not significant"
These results are practically identical! The difference between p = .049 and p = .051 is trivial, but we treat them completely differently. Focus on effect sizes and CIs instead.

The sharp cutoff at p = .05 is arbitrary and misleading. Results just above or below .05 provide similar evidence. Report exact p-values, focus on effect sizes and confidence intervals, and interpret results on a continuum rather than dichotomously.

Language Matters

🚫 Problematic Language
"The treatment proved to be effective"
"We failed to find an effect"
"The results approached significance"
✓ Better Language
"The treatment group improved more, d = 0.45, 95% CI [0.12, 0.78]"
"The effect was small and imprecisely estimated, d = 0.15, 95% CI [-0.18, 0.48]"

Avoid language that overstates conclusions. 'Proved' is too strong - we have evidence, not proof. 'Failed to find' implies we should have - a null result might be true. 'Approached significance' is meaningless. Be precise about what the data show.

Reporting Checklist

Before Submitting, Check:
✓
Sample sizes for all analyses
✓
Descriptive statistics (M, SD) for all variables
✓
Test statistics with degrees of freedom
✓
Exact p-values (or p < .001)
✓
Effect sizes with confidence intervals
✓
ALL planned analyses reported
✓
Exploratory analyses labeled as such

Use a reporting checklist to ensure completeness. Guidelines like JARS (APA), CONSORT (trials), and STROBE (observational studies) provide detailed checklists for specific study types.

★

Real-World Examples

Apply your knowledge to practical scenarios

01

Improving a Thesis Results Section

A student writes: 'The t-test was significant (p < .05). This proves our hypothesis that the drug works.' The advisor asks them to revise according to APA guidelines and best practices.

Sample Data
{
  "original": "t-test was significant (p < .05)",
  "sample_sizes": "n = 25 per group",
  "means": "Treatment M = 72.3, Control M = 65.8",
  "sds": "Treatment SD = 14.2, Control SD = 13.8",
  "actual_p": "p = .032"
}
Q What's wrong with the original statement? +
A Missing: sample sizes, descriptive statistics, test statistic with df, exact p-value, effect size, CI. Also: 'proves' is too strong, and doesn't report what the actual finding means.
Q How should it be revised? +
A Revised: 'Participants in the treatment group (n = 25, M = 72.3, SD = 14.2) scored higher than controls (n = 25, M = 65.8, SD = 13.8), t(48) = 2.21, p = .032, d = 0.46, 95% CI [0.04, 0.88], a small-to-medium effect.'
Key Insights
  • Always include n, M, SD for each group
  • Report exact p-values and effect sizes with CIs
  • Interpret effect size magnitude in practical terms
02

Clinical Trial Reporting (CONSORT)

A pharmaceutical company reports trial results. They need to follow CONSORT guidelines: flow diagram showing participant flow, intention-to-treat analysis, all randomized participants accounted for, adverse events reported.

Sample Data
{
  "enrolled": 500,
  "randomized_treatment": 252,
  "randomized_control": 248,
  "completed_treatment": 218,
  "completed_control": 231,
  "analyzed_treatment": 252,
  "analyzed_control": 248,
  "analysis": "Intention-to-treat with multiple imputation"
}
Q Why analyze all 500 randomized participants when only 449 completed? +
A Intention-to-treat (ITT) analysis includes ALL randomized participants regardless of completion. This preserves the benefits of randomization and avoids bias from differential dropout. Missing data should be handled properly (e.g., multiple imputation).
Q What must be in the CONSORT flow diagram? +
A The flow diagram shows: assessed for eligibility → excluded (with reasons) → randomized → allocated to each arm → received treatment → lost to follow-up (with reasons) → analyzed. It ensures full transparency about the sample.
Key Insights
  • CONSORT ensures complete, transparent trial reporting
  • Flow diagrams show what happened to every participant
  • ITT analysis preserves randomization benefits
03

Pre-Registered Replication

Researchers conduct a pre-registered replication of a famous psychology finding. Their pre-registration specifies: exact procedures, sample size (n = 200, based on power analysis), primary DV, analysis plan. Results: d = 0.12, 95% CI [-0.08, 0.32], compared to original d = 0.65.

Sample Data
{
  "original_d": 0.65,
  "replication_d": 0.12,
  "replication_ci": "[-0.08, 0.32]",
  "replication_p": ".24",
  "replication_n": 200,
  "original_n": 40
}
Q How should the replication failure be interpreted? +
A The replication CI excludes the original effect size (0.65) but includes zero. This suggests either: the original was a false positive or overestimate, or there are important moderators. The replication had MORE power, so small effects should have been detected.
Q Why might the original effect have been overestimated? +
A Small-sample studies that reach significance tend to overestimate effects (winner's curse). With n = 40, the original could only detect large effects, so any significant finding was necessarily large. Publication bias means non-significant replications weren't published.
Key Insights
  • Pre-registration prevents p-hacking in replications
  • Small original samples often overestimate effects
  • Report effect sizes and CIs to compare original vs replication
?

Statistical Reporting Quiz

Test your understanding • Passing score: 70%

0 of 10 answered
Q1 multiple-choice

According to APA style, which is the correct way to report a p-value of 0.023?

Explanation: APA style omits the leading zero for statistics that cannot exceed 1 (like p-values, correlations). Use lowercase italic p. Report exact values unless p < .001.
Q2 multiple-choice

A complete t-test report should include all of the following EXCEPT:

Explanation: While power analysis should be conducted before the study, it's typically reported in the Method section, not with each statistical result. The Results section needs descriptives, test stats, p-values, and effect sizes.
Q3 multiple-choice

What is the main purpose of pre-registration?

Explanation: Pre-registration commits researchers to their analysis plan before seeing results. This prevents p-hacking (trying many tests until finding significance) and HARKing (Hypothesizing After Results are Known).
Q4 multiple-choice

When reporting error bars, you should always:

Explanation: Different error bars (SD, SE, CI) show different things and cannot be directly compared. Always explicitly state which type you're using so readers can interpret correctly.
Q5 multiple-choice

Why is the phrase 'approached significance' problematic?

Explanation: 'Approached significance' (for p = .06 or .07) implies something special about results near .05. In reality, p = .06 is very similar evidence to p = .04. This phrase perpetuates the false dichotomy around p = .05.
Q6 multiple-choice

For ANOVA, which effect size measure is most commonly reported?

Explanation: Partial eta-squared (η²ₚ) is the standard effect size for ANOVA, representing variance explained by a factor relative to that factor plus error. Cohen's d is for comparing two means.
Q7 multiple-choice

What should you do if exploratory analyses (not pre-registered) yield significant findings?

Explanation: Exploratory findings are valuable but must be clearly labeled as such. This helps readers understand the evidence is weaker (more prone to false positives) and that replication is needed.
Q8 multiple-choice

A 95% confidence interval for Cohen's d of [0.15, 0.85] indicates:

Explanation: Since the CI excludes zero (both bounds are positive), the effect is statistically significant. The effect could be anywhere from small (0.15) to large (0.85), indicating some imprecision.
Q9 multiple-choice

Which visualization practice should be AVOIDED?

Explanation: Truncating the y-axis (not starting at zero) visually exaggerates differences. A change that looks dramatic on a truncated axis might be trivially small on a full scale. This is a common way to mislead readers.
Q10 multiple-choice

CONSORT guidelines are specifically designed for reporting:

Explanation: CONSORT (Consolidated Standards of Reporting Trials) provides a checklist and flow diagram specifically for randomized controlled trials. Other guidelines include STROBE (observational studies) and PRISMA (systematic reviews).

Quiz Results

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