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Free Sample Size and Power Analysis Calculator for Researchers

Determine the exact number of participants needed for statistically valid studies. Our free sample size and power analysis calculator uses validated formulas from G*Power and methods recommended by PubMed and Cochrane.

15
Statistical Tests
100%
Free Forever
5K+
Researchers

Supported Tests

μ T-Tests
F ANOVA
χ² Chi-Square
S Survival
≡ Non-Inferiority
= Equivalence
r Correlation
β Regression
◐ ROC/AUC
Se Sensitivity
Calculate to the standards expected by journals including: PubMed Cochrane NEJM Lancet BMJ
100% Free
Typical Values & Examples
10%

Quick Guide

  • Select your study design from the dropdown
  • Enter the expected effect size or group parameters
  • Adjust dropout rate if participants may leave the study
  • Click Calculate to see required sample size

Tip: Hover over the (?) icons for detailed explanations of each parameter.

How to Use: Choose Your Statistical Test

Select the appropriate test based on your study design and data type

Tests for Comparing Means

Two-Sample T-Test

When to use: Comparing means between two independent groups

Typical values:

  • Blood pressure: Mean diff = 5-10 mmHg, SD = 12-15
  • HbA1c: Mean diff = 0.5-1.0%, SD = 1.2-1.5

Paired T-Test

When to use: Before/after measurements on same subjects

Typical values:

  • Pain score: Mean diff = 2, SD of diff = 3
  • BP after treatment: Mean diff = 10 mmHg, SD = 12

One-Sample T-Test

When to use: Compare sample mean to known reference

Typical values:

  • Reference = 100, Expected = 105, SD = 15

ANOVA (3+ Groups)

When to use: Comparing means across 3+ groups

Effect size (Cohen’s f):

  • Small: 0.10 | Medium: 0.25 | Large: 0.40

Tests for Comparing Proportions

Two Proportions (Chi-Square)

When to use: Comparing rates between two groups

Typical values:

  • Response: Control = 30%, Treatment = 50%
  • Adverse events: Drug A = 15%, Drug B = 8%

Single Proportion

When to use: Compare observed rate to known value

Typical values:

  • Historical = 20%, Expected = 12%

Clinical Trial Designs

Superiority Trial

When to use: Prove new treatment is better than control

  • Mean diff = 10, SD = 20

Non-Inferiority Trial

When to use: Prove new treatment is not worse

  • Margin = -10% (clinically acceptable)

Equivalence Trial

When to use: Prove treatments are equal (bioequivalence)

  • Margin = ±20% or ±15%

Survival Analysis

Log-Rank Test

When to use: Time-to-event analysis

  • Overall survival: HR = 0.75, Event rate = 30%
  • Progression-free: HR = 0.65, Event rate = 50%

Correlation & Regression

Correlation

Correlation strength (r):

  • Small: 0.10 | Medium: 0.30 | Large: 0.50

Linear Regression

Effect size (R²):

  • Small: 0.10 | Medium: 0.25 | Large: 0.40

Logistic Regression

Rule: 10-20 events per predictor

Diagnostic Studies

Sensitivity/Specificity

  • Screening: Sensitivity = 90%, Precision = ±5%
  • Confirmatory: Specificity = 95%, Precision = ±3%

ROC Curve (AUC)

  • AUC 0.50 = Random | 0.70-0.80 = Acceptable | >0.80 = Excellent

How We Compare: Editverse vs Other Calculators

See why researchers choose Editverse for power analysis

FeatureEditverseG*PowerPS PowerOpenEpiSealed Envelope
Price✓ FreeFreeFreeFreeFreemium
Platform✓ Web (No Download)Desktop onlyDesktop onlyWebWeb
Mobile Friendly✓ Yes✗ No✗ NoLimitedLimited
Clinical Trial Designs✓ All 3 TypesLimitedYes✗ NoYes
Survival Analysis✓ Log-RankYesYes✗ NoLimited
Interactive Charts✓ YesYes✗ No✗ No✗ No
Publication Reports✓ Yes✗ No✗ No✗ No✗ No
Dropout Adjustment✓ Built-inManualManual✗ NoYes
ROC/AUC✓ Yes✗ No✗ No✗ No✗ No
Registration✓ Not RequiredNoNoNoSome features
Why choose Editverse? Our calculator combines statistical rigor of desktop apps with web convenience. Designed for medical researchers with publication-ready methodology text that other calculators don’t offer.

How to Cite This Calculator

Use these formats for your methodology section, ethics applications, and publications

📝 In-Text (Methods Section)

Sample size was calculated using the Editverse Sample Size Calculator (Editverse, 2025), a validated online power analysis tool for medical research.

📚 APA 7th Edition

Editverse. (2025). Editverse Sample Size Calculator [Online tool]. https://editverse.com/free-sample-size-calculator-power-analysis-tool-for-researchers/

📖 Vancouver/ICMJE

Editverse. Editverse Sample Size Calculator [Internet]. 2025 [cited 2025 Jan 6]. Available from: https://editverse.com/free-sample-size-calculator-power-analysis-tool-for-researchers/

🔬 Full Methodology Example

Sample Size Calculation: The required sample size was determined using the Editverse Sample Size Calculator (https://editverse.com). Based on a two-sample t-test with α = 0.05, 80% power, mean difference of 10 units, and SD of 25 units, we calculated 78 participants per group (156 total). Accounting for 20% dropout, we planned to enroll 196 total.

💡 Tips for Ethics Committees & Grant Applications

  • Justify effect size: Reference pilot data or published literature
  • Explain alpha and power: Standard is α=0.05, power=80%
  • Account for dropouts: Use our built-in dropout slider
  • Include parameters: Reviewers want to verify your numbers
  • Use Report feature: Generate publication-ready text with one click

Power Analysis Calculator for Research Studies

Power analysis is used to estimate the minimum sample size required to detect a statistically meaningful effect while controlling the probability of Type I and Type II errors. A Type I error (false positive) occurs when a study incorrectly concludes an effect exists; a Type II error (false negative) occurs when a true effect is missed. Most biomedical and clinical studies target 80% power (1-β = 0.80) at a significance level of α = 0.05.

Using this power analysis calculator, researchers specify the expected effect size, significance level, desired power, and study design. The calculator then returns the required sample size. Running a power analysis before data collection ensures that a study is neither underpowered — risking a false negative — nor unnecessarily large, which wastes resources and raises ethical concerns about unnecessary participant recruitment.

Effect sizes can be derived from pilot data, published literature, or the minimum clinically important difference. Cohen’s conventions (small: d = 0.2, medium: d = 0.5, large: d = 0.8 for t-tests; f = 0.10/0.25/0.40 for ANOVA) provide a starting point when no prior data exists.

Run Power Analysis ↑

Sample Size Calculator for Clinical Trials

Clinical trials require rigorous sample size calculation before recruitment begins. Underpowered trials may fail to detect real treatment differences, while oversized trials expose more participants to experimental conditions than necessary. Ethics committees and grant bodies require a clearly justified sample size calculation as part of protocol approval.

This calculator supports three core clinical trial designs. Superiority trials test whether a new treatment is better than a control; the required inputs are expected mean difference, standard deviation, significance level, and desired power. Non-inferiority trials test whether a new treatment is not unacceptably worse than an established standard; the key additional parameter is the non-inferiority margin. Equivalence trials test whether two treatments produce the same effect within a defined boundary.

For survival-based clinical trials, the calculator uses the log-rank test formula, requiring the expected hazard ratio, event rate, and follow-up duration.

Key inputs for clinical trial calculations

  • Expected treatment difference or hazard ratio
  • Standard deviation (for continuous outcomes)
  • Significance level: typically α = 0.05
  • Statistical power: typically 80% or 90%
  • Allocation ratio (e.g., 1:1 or 2:1)
  • Non-inferiority or equivalence margin (where applicable)
  • Expected dropout rate (use the built-in dropout slider)
Calculate Clinical Trial Sample Size ↑

Prevalence Sample Size Calculator

Prevalence-based sample size calculation is used in cross-sectional and epidemiological studies where the primary objective is to estimate the proportion of a population with a specific condition, exposure, or characteristic. Unlike comparative studies, these designs do not test a hypothesis between groups — instead, they estimate a population parameter with a specified level of precision.

The required sample size for a prevalence study depends on the expected prevalence (p), the acceptable margin of error (d), and the confidence level (typically 95%, corresponding to Z = 1.96). When the study population is finite and relatively small, a finite population correction factor reduces the required sample size.

Using the Single Proportion option in the calculator, researchers can model prevalence studies directly. A common example: estimating the prevalence of hypertension in an urban clinic with an expected prevalence of 30%, a margin of error of 5%, and 95% confidence requires approximately 323 participants before accounting for non-response.

Typical inputs for prevalence calculations

  • Expected prevalence: e.g., 30% (or use 50% for maximum conservatism)
  • Margin of error: typically 5% for general studies, 3% for precision studies
  • Confidence level: 95% (Z = 1.96) or 99% (Z = 2.576)
  • Population size: enter if finite population correction applies
Calculate Prevalence Sample Size ↑

Sample Size Calculator for T-Tests

T-test sample size calculation applies when comparing means between one group and a reference value, two independent groups, or paired measurements on the same subjects. The three t-test designs — one-sample, two-sample (independent), and paired — differ in their input parameters and the interpretation of sample size output.

For a two-sample t-test, the required sample size per group depends on the expected mean difference between groups, the pooled standard deviation, significance level, power, and test direction. For a paired t-test, the key parameter is the mean difference between paired measurements and its standard deviation — typically smaller than the between-subjects standard deviation, which is why paired designs are statistically efficient.

Typical parameter values for t-test calculations

  • Blood pressure study: Mean diff = 5–10 mmHg, SD = 12–15
  • HbA1c study: Mean diff = 0.5–1.0%, SD = 1.2–1.5
  • Weight loss trial: Placebo = 0 kg, Drug = −5 kg, SD = 8
  • Cohen’s d conventions: Small = 0.2, Medium = 0.5, Large = 0.8
Calculate T-Test Sample Size ↑

Sample Size Calculator for ANOVA

ANOVA sample size calculation is used when a study compares means across three or more groups simultaneously. Rather than running multiple t-tests — which inflates the Type I error rate — ANOVA tests the overall null hypothesis that all group means are equal in a single analysis.

The key parameter is Cohen’s f, the effect size measure for ANOVA. Small: f = 0.10; medium: f = 0.25; large: f = 0.40. The calculator returns the total sample size required and the per-group breakdown.

ANOVA parameter reference

  • Number of groups: e.g., 3 (control + 2 interventions)
  • Effect size (Cohen’s f): Small 0.10 | Medium 0.25 | Large 0.40
  • Significance level: α = 0.05
  • Power: 80% or 90%
Calculate ANOVA Sample Size ↑

Sample Size Calculator for Chi-Square Tests

Chi-square sample size calculation is used in studies involving categorical outcomes — for example, comparing response rates, complication rates, or disease prevalence between two groups. For a two-proportion chi-square test, the required inputs are the expected proportions in each group, the significance level, and the desired power.

Cohen’s w conventions: small = 0.10, medium = 0.30, large = 0.50. A practical example: comparing adverse event rates of 15% vs 8% at 80% power and α = 0.05 requires approximately 300 participants per group before dropout adjustment.

Typical inputs for chi-square calculations

  • Control proportion: e.g., 30% response rate
  • Treatment proportion: e.g., 50% response rate
  • Effect size (Cohen’s w): Small 0.10 | Medium 0.30 | Large 0.50
  • Significance level: α = 0.05
  • Power: 80%
Calculate Chi-Square Sample Size ↑

Frequently Asked Questions

What is sample size calculation?

Sample size calculation determines the minimum participants needed to detect a statistically significant effect. It ensures adequate power while avoiding unnecessary recruitment.

How do I calculate sample size for a clinical trial?

Select your trial design, enter expected treatment difference, standard deviation, significance level (α=0.05), and power (80%). Our calculator computes required participants per arm.

What is statistical power?

Statistical power (1-β) is the probability of detecting a true effect. 80% power means 80% chance of finding significance if the effect is real. Higher power needs larger samples.

What effect size should I use?

Base effect size on: (1) pilot data, (2) published literature, or (3) minimum clinically important difference. Cohen’s d: 0.2=small, 0.5=medium, 0.8=large.

Is this calculator free?

Yes! 100% free for academic and commercial use. No registration, no download, no limitations. Use directly in your browser.

How accurate vs G*Power?

We use the same validated statistical formulas. Results are equivalent for same inputs. Advantage: web-based access without installation.

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