Power Analysis Calculator

Enter your significance level (α), statistical power (1-β), effect size (d), and allocation ratio to find the minimum sample size needed for your study. The Power Analysis Calculator returns the required sample size per group, total subjects, and a visual breakdown — so you can design studies with confidence before data collection begins.

Probability of a Type I error (false positive). Commonly set to 0.05.

Probability of correctly detecting a true effect. 0.80 (80%) is the standard minimum.

d

Small ≈ 0.2, Medium ≈ 0.5, Large ≈ 0.8. Use pilot data or published literature.

Ratio of subjects in Group 2 vs Group 1. Use 1 for equal group sizes.

Two-tailed tests detect effects in either direction. One-tailed tests are used when the effect direction is predetermined.

%

Inflate sample size to account for participant attrition. Set to 0 if not applicable.

Results

Sample Size per Group (n₁)

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Group 2 Sample Size (n₂)

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Total Sample Size

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n₁ Adjusted for Dropout

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Total Adjusted for Dropout

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Achieved Power

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Sample Size Breakdown

Frequently Asked Questions

What is statistical power and why does it matter?

Statistical power (1-β) is the probability that a study will correctly detect a true effect when one exists. Low power means your study may miss a real difference — a false negative (Type II error). A power of 0.80 (80%) is the widely accepted minimum in most research fields, meaning there is an 80% chance of detecting a true effect of the specified size.

What is effect size and how do I choose a value?

Effect size (Cohen's d) quantifies the magnitude of the difference between groups relative to variability. By convention, d = 0.2 is small, d = 0.5 is medium, and d = 0.8 is large. The best approach is to base effect size on pilot study data or published literature from similar studies. When no prior data exist, a medium effect size (0.5) is a common default.

What significance level (α) should I use?

The significance level α is the probability of a Type I error — concluding an effect exists when it does not. The conventional threshold is α = 0.05 (5%), meaning you accept a 5% risk of a false positive. For high-stakes clinical research or multiple testing scenarios, α = 0.01 is sometimes used. Lowering α requires a larger sample size to maintain power.

What is the allocation ratio and when should it differ from 1?

The allocation ratio (n₂/n₁) defines how many participants are in Group 2 relative to Group 1. A ratio of 1 means equal group sizes, which is most statistically efficient. Unequal ratios (e.g., 2:1) are used when one group is harder or more expensive to recruit, or when ethical constraints limit exposure to an experimental treatment.

Should I use a one-tailed or two-tailed test?

A two-tailed test is appropriate when you want to detect a difference in either direction — whether Group 1 is higher or lower than Group 2. A one-tailed test is used only when theory or prior evidence firmly establishes the direction of the expected effect before data collection. Two-tailed tests are the standard default and are more conservative.

Why should I account for dropout rate?

Participant attrition is common in longitudinal and clinical studies. If you enroll exactly the calculated minimum and some participants drop out, your effective sample falls below the required size — reducing power and potentially invalidating your conclusions. Inflating the enrollment target by your expected dropout rate (e.g., 10–20%) protects the integrity of your study.

What is the relationship between sample size and statistical power?

Sample size and power are directly related: larger samples yield greater power for the same effect size and significance level. Conversely, a small sample may be underpowered, producing unreliable results. This calculator uses the standard normal approximation formula to find the exact minimum n that achieves your desired power.

Can this calculator be used for clinical trials and medical research?

Yes, this calculator applies the widely accepted two-sample independent means formula based on the normal distribution, which is standard in medical, clinical, and behavioral research. For specialized designs — such as crossover trials, survival analysis, or cluster-randomized trials — consult a biostatistician, as additional adjustments beyond this tool may be required.

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