Section 3.5

Writing About Non-Significant Results

Sooner or later a test comes back p = .08, and you will be tempted to call it "a trend toward significance" and move on. Don't. A non-significant result is not a failure, and it is not proof that the effect is zero. It is a specific finding that you can report, and reporting it accurately is a sign of a careful researcher. This lesson explains what these results mean and how to write about them without over- or under-claiming.

"Not significant" is not "no effect"

The most serious mistake is treating p > .05 as evidence that nothing is there. Absence of evidence is not evidence of absence. A high p-value can mean that the effect is near zero, or that your study was too small to detect a real effect (see The Logic of Hypothesis Testing). The p-value alone can't tell those two situations apart. So "we found no effect" is almost always the wrong sentence. What you found is that you couldn't rule the null out, which is a much weaker claim.

There is no "trend toward significance"

"Marginally significant," "approaching significance," "a trend toward…": these phrases present a non-significant result as if it had crossed a line it did not cross. A p of .06 is not "nearly significant": significance is a yes/no threshold you chose in advance, and .06 is on the "no" side. The phrases are also used in only one direction. Researchers do not write that p = .04 "only marginally" reached significance. Report the exact p-value instead: "p = .06" is accurate and informative, while "a trend toward significance" is spin.

What to write instead

A good sentence about a non-significant result includes three things the bare p-value leaves out:

  • The effect size and its confidence interval. "d = 0.15, 95% CI [−0.29, 0.59]" tells the reader both your best estimate and how uncertain it is. The CI matters most here, because it shows the whole range of effects your data are compatible with.
  • Power or precision context. Was the study big enough to catch the effect you cared about? A wide CI that spans from "meaningfully negative" to "meaningfully positive" is your signal to say the study was underpowered, not that the effect is absent.
  • Neutral framing. Write "The difference was not significant," then describe the interval. Don't apologize, add spin, or hide the result.

When you can say "no meaningful effect"

Sometimes a null result is informative: when the confidence interval is narrow and close to zero. If d = 0.05 with a 95% CI of [−0.15, 0.25], you've effectively ruled out anything beyond a small effect, and you're entitled to say the difference is negligible. This is the intuition behind equivalence testing: instead of asking "is the effect exactly zero?", you ask "can I rule out effects big enough to matter?" A precise null result answers yes. A wide one answers "I don't know yet". So the same p > .05 can come from very different situations, and only the CI shows which one you have.

A non-significant result is also not unpublishable, and the study is not wasted. Well-designed null studies correct the record, contribute to meta-analyses, and stop others from chasing effects that aren't there.

Testing for equivalence: TOST

"Rule out effects big enough to matter" is a test you can run. It is called two one-sided tests, or TOST. You supply a bound, and the procedure tells you whether the effect is inside it.

You choose the bound, and you must choose it before you look: the smallest effect size of interest, the point below which you would not care even if the effect were real. It is a substantive decision, not a statistical one, so no formula can give it to you. Suppose you set it at d = 0.3 for the tight null above. TOST then runs two one-sided tests at once, one against "the effect is −0.3 or lower" and one against "the effect is +0.3 or higher", and reports the larger of the two p-values. Reject both and you have evidence that the effect, whatever its sign, is too small to matter.

Run it on the two studies this lesson has been comparing, both of them non-significant:

  • The tight one (d = 0.05, 200 per group, 95% CI [−0.15, 0.25]). Against ±0.3 the TOST p is .006. Equivalence declared: the data are incompatible with anything you would call an effect.
  • The wide one (d = 0.15, 40 per group, 95% CI [−0.29, 0.59]). Same bound, TOST p = .25. Equivalence cannot be declared. The study cannot rule out a difference that matters, and at this sample size it never could.

A shortcut explains a number that surprises people: at α = .05, TOST succeeds exactly when the 90% confidence interval falls entirely inside your bounds, not the 95% one. Each of the two one-sided tests puts 5% in a single tail, and a 90% interval leaves exactly 5% in each tail. For the tight study that interval is [−0.11, 0.21], well inside ±0.3. For the wide study it runs [−0.22, 0.52] and goes past the upper bound.

You can't run TOST after the fact with a bound chosen to make the numbers work. Set the bound when you set the hypothesis, and say in the Methods that you did. Preregistration & Open Science covers how to record it in advance.

Pick the honest sentence

Here are five studies, all non-significant, that don't all mean the same thing. Read each result card (the p-value, the effect size, and especially the confidence interval), then choose the one sentence that reports it accurately. The others overclaim, dismiss the result, or reach for "a trend."

⚖️ Which sentence is honest?

Five results, all "not significant," that mean different things. Use the interval to decide.

The interval tells you which sentence to write. A wide interval that includes zero means "underpowered, can't tell," not "no effect." A narrow interval close to zero means "we can rule out anything that matters." Two results with the same p > .05 can need opposite sentences, and only the interval tells you which.

Why it matters: graders and reviewers pay close attention to how you write about a null result. If you call p = .08 "a trend," you tell the reader that you will bend language to get the result you wanted. If you report the effect size and the interval in neutral wording, a reader has reason to believe your significant results too.

Problem 100 of the practice problems puts this lesson inside an APA formatting exercise. Three of the four things wrong with its sentence are formatting, and the fourth is the phrase “were more accurate” attached to p = .062.

Common questions

How do I report a non-significant result in APA style?

Report it exactly like a significant one, and never hide or soften it. Give the test statistic, degrees of freedom, and the exact p-value, then the effect size and its confidence interval: "The groups did not differ significantly, t(58) = 1.30, p = .20, d = 0.34, 95% CI [−0.18, 0.84]." The confidence interval is the important part, since it shows which effects your data are compatible with. Call the result "not significant" and, if the interval is wide, say that the study was underpowered, not that there is no effect.

Can I say a result was 'marginally significant' or 'a trend toward significance'?

No. Significance is a yes/no threshold you set in advance, so a p of .06 is on the 'no' side. It is not 'nearly significant', and there is no such thing as 'marginally significant'. The phrase is only ever used to push a non-significant result upward. Researchers don't write that p = .04 'only marginally' reached significance. Report the exact p-value, the effect size, and the confidence interval, and interpret them without spin. If the point estimate looks promising but the interval includes zero, say the result is inconclusive and needs a larger, ideally preregistered, study.

I want to claim there is no effect. Equivalence test or Bayes factor?

Either can do what a p-value cannot: give you evidence for a null, not just a failure to reject it. They ask different questions, so pick the one that asks yours. An equivalence test (TOST) asks whether the effect is smaller than a bound you name in advance, and it answers with an ordinary p-value. The hard part is the bound, because you have to decide what counts as too small to care about before you look. A Bayes factor asks how much more probable your data are under one hypothesis than the other. Its hard part is the prior, because "the effect exists" has to be specified as a distribution before the ratio means anything. Both are in JASP: the Equivalence T-Tests module offers a frequentist TOST and a Bayesian version side by side. Reviewers accept either, provided you say which bound or which prior you chose, and when you chose it.