Sample size matters: a practical guide for development practitioners

"How many households should we survey?" This is perhaps the most common, and most consequential, question in impact evaluation design. Get it wrong, and you risk either wasting resources on an oversized study or, worse, collecting data that can't detect your programme's effects even if they exist.

This guide explains the core concepts of sample size calculation without the jargon, and provides practical guidance for development practitioners designing evaluations. Getting this right is a cornerstone of data-driven decision making in the development sector.

The core problem

At its heart, sample size is about detecting real effects (signal) amid natural variation (noise). Your sample size determines your ability to distinguish signal from noise.

If your sample is too small, even real programme effects can get lost in the noise. You'll conclude "no significant effect" when the programme actually worked, which is a costly mistake for learning and accountability.

Signal vs noise in sample size
[Illustration 1: Signal vs Noise]
Sample size determines your ability to detect real effects

Four key concepts

Statistical Power
The probability that your study will detect an effect if an effect actually exists. Standard target: 80%.
Significance Level (α)
Probability of concluding there's an effect when there isn't (false positive). Standard: 5% (α = 0.05).
Effect Size
How big a change your programme is expected to create. Larger effects are easier to detect; smaller effects need bigger samples.
Variance
How spread out the outcome is in your population. Higher variance makes effects harder to detect.

The intuition:

  • Bigger effect → need fewer observations (signal is louder)
  • More variance → need more observations (noise is louder)
  • Higher power wanted → need more observations (want more certainty)
  • Lower significance level → need more observations (stricter threshold)

The defaults above, 80% power and a 5% significance level, are conventions, not laws of nature. They trace back to Jacob Cohen's argument that, absent a specific reason to choose otherwise, treating a Type I error (false positive) as four times more serious than a Type II error (false negative) implies roughly these values (Cohen, 1988). J-PAL's power guidance likewise notes that most studies aim for power of 80% or higher. If the cost of missing a real effect is unusually high, it can be worth powering above 80%.

The basic formula

For a simplified two-group comparison, sample size can be calculated as:

Sample Size Formula
n = 2 × [(Zα + Zβ)² × σ²] / δ²

n = sample size per group

Zα = Z-score for significance level (1.96 for α = 0.05)

Zβ = Z-score for power (0.84 for 80% power)

σ² = variance of outcome

δ = minimum detectable effect (MDE)

Key insight: The effect size (δ) is in the denominator and squared. This means that halving your expected effect size quadruples your required sample size.

Effect size: the hardest part

Choosing an appropriate effect size is typically the most challenging part of sample size calculation. There are three approaches:

  1. Prior evidence: What have similar interventions achieved? Reviewing evidence from well-chosen indicators in comparable programmes helps. (Caution: publication bias often inflates reported effects.) J-PAL's quick guide to power calculations calls choosing the minimum detectable effect "the hardest part" and says there is no universal rule of thumb for a good one: it depends on what is meaningful to the parties involved, weighed against the opportunity cost of doing the research.
  2. Minimum meaningful effect: What's the smallest change that would matter given your programme's cost? In a widely-shared World Bank Development Impact post, Berk Özler argues that an MDE stated only in standard deviations (e.g. "0.3 SD") is typically insufficient: translate it into the units of the outcome and ask whether a change that size is worth detecting. His example is a 0.3 SD effect on monthly consumption, which comes to only 5% of the mean where the standard deviation is one-sixth of the mean.
  3. Standardised conventions: As a last resort, Cohen's benchmarks treat a standardised effect (Cohen's d) of 0.2 SD as "small," 0.5 SD as "medium," and 0.8 SD as "large" (Cohen, Statistical Power Analysis for the Behavioral Sciences, 2nd ed., 1988). Cohen himself stressed these cut-offs were arbitrary and a fallback when domain-specific guidance is absent; in practice, as Özler notes in the post above, many interventions do not produce impacts above 0.1 to 0.2 SD.
️ Warning
Don't work backward from your budget ("we can afford 200 surveys, what effect can we detect?"). This often yields implausibly large MDEs that set up the evaluation to fail. The World Bank's DIME Wiki frames the MDE as the smallest true effect a design can reliably distinguish from zero. If that threshold sits above any effect your programme could plausibly produce, the study is set up to find "nothing" before it begins.

Cluster randomisation complications

In many development programmes, you can't randomly assign individuals: you must randomise at the village, school, or clinic level. This creates intra-cluster correlation (ICC), which dramatically increases required sample size (see the table below). J-PAL's power guidance notes that designs randomising at more granular levels generally have greater statistical power, and that calculations should explicitly incorporate within- and between-cluster variance.

The Design Effect captures this inflation. In its standard form, DE = 1 + (m − 1) × ICC, where m is the cluster size. The ICC that the formula depends on is explained in Kerry & Bland's 1998 BMJ note on the intracluster correlation coefficient (BMJ 1998;316:1455):

Design Effect
DE = 1 + (cluster size - 1) × ICC
ICC Cluster=10 Cluster=20 Cluster=50
0.01 1.09 1.19 1.49
0.05 1.45 1.95 3.45
0.10 1.90 2.90 5.90
0.20 2.80 4.80 10.80

The message: Cluster randomisation is expensive. Adding respondents within a cluster yields diminishing returns to power (once the ICC is positive, extra observations in the same cluster carry overlapping information), so adding clusters usually buys more power than enlarging the ones you have. Hemming and colleagues' guide to designing efficient cluster randomised trials works through exactly this trade-off, and recommends choosing the number of clusters and the cluster size together rather than one at a time (Hemming et al., BMJ, 2017).

Sample size calculation workflow
[Illustration 2: Sample size workflow]
The complete sample size calculation process

A worked example

Agricultural extension programme

Baseline: 2,000 kg/hectare yield, SD 600 kg | Expected effect: 10% increase (200 kg) | Power: 80%, Significance: 5% | ICC: 0.05, Households per village: 15, Expected attrition: 10%

1 Basic sample size: Using the formula = 142 per group
2 Adjust for clustering: DE = 1 + (15-1) × 0.05 = 1.70 → 142 × 1.70 = 241 per group
3 Adjust for attrition: 241 ÷ (1 - 0.10) = 268 per group
4 Convert to clusters: 268 ÷ 15 = 18 villages per group
Required Sample
36 villages, 540 households

vs. 284 from naïve formula ignoring clustering and attrition

Rules of thumb

Sample size sanity checks

Small effects (0.2 SD): roughly 400 per group at the conventional 80% power and 5% significance, which falls straight out of the formula
Medium effects (0.5 SD): plan for roughly 65 per group at the same conventions
Cluster RCTs: the more clusters the better; treatments of cluster design (e.g. Hemming et al., 2017) warn that very few clusters per arm leaves estimates fragile, and trials with a handful of clusters can usually only detect large effects. Taljaard and colleagues (Clinical Trials, 2016) describe the substantial risks associated with designs that have few clusters
Always inflate for attrition (typically 10-20%), using a rate taken from comparable surveys in your context or from a pilot
If calculated sample is surprisingly small, double-check assumptions
If budget only allows small samples, consider qualitative methods instead

What if you can't afford adequate power?

Sometimes the honest answer is that rigorous impact evaluation isn't feasible given resources. Options include:

  • Pool resources across organisations or sites
  • Change the question: a well-powered process evaluation may be better than an underpowered impact evaluation
  • Focus on larger effects: can you intensify the intervention in fewer sites?
  • Accept uncertainty: an underpowered study with transparent limitations is better than no evidence, if expectations are managed. Being upfront about these trade-offs is part of ethical research practice
An underpowered study wastes money, and it wastes everyone's time, including your participants'. You've collected their data, disrupted their days, and learned nothing useful.

Tools and resources

Several tools can help with sample size calculations:

  • G*Power: Free software for various study designs
  • Optimal Design: For multilevel and cluster randomised designs
  • PowerUp!: Excel-based, from Dong and Maynard (2013), for experimental and quasi-experimental designs
  • ImpactMojo Sampling Design Studio: A guided sampling studio for MEL practitioners in South Asia, with a built-in ICC reference library and a cluster-size optimiser that takes costs in rupees

For a book-length treatment that walks through statistical power for development evaluations, the standard practitioner reference is Rachel Glennerster and Kudzai Takavarasha's Running Randomized Evaluations: A Practical Guide (Princeton University Press, 2013), whose power chapter draws directly on J-PAL's field experience. J-PAL's own power calculations guide and the World Bank's DIME Wiki page on power calculations are concise, freely available companions.

Getting sample size right is one of the most important decisions in evaluation design. Pair it with good survey design and attention to data quality in the field, and you'll have a solid foundation for credible evidence. Our free Impact Evaluation 101 deck covers power and sampling in context, and the full Causal Inference for Development course goes deeper.