Estimating the Reproducibility of Psychological Science

Open Science Collaboration (2015), Science 349:aac4716

3R course, Padova 2026

May 18, 2026

Outline

  1. Background — the replicability debate in psychology
  2. Background — the Open Science Collaboration
  3. Question and design
  4. Methods — study selection, protocol, success criteria
  5. Results — significance, effect sizes, scatterplots, moderators
  6. Discussion — interpretation, critiques, implications
  7. Questions for the room

Background

The replicability debate in psychology

  • Ioannidis (2005) — “Why most published research findings are false”: low power × selection × flexibility ⇒ many published claims are false.
  • Bem (2011, JPSP) — nine experiments reporting evidence for precognition, published with conventional standards. A wake-up call for the field.
  • Simmons, Nelson & Simonsohn (2011)False-positive psychology: undisclosed researcher degrees of freedom inflate Type I error far above 5%.
  • Stapel (2011) and other fraud cases sharpen attention on data integrity.
  • Failed direct replications of high-profile findings (e.g. social priming: Doyen et al. 2012 on Bargh) accumulate.
  • Many Labs 1 (Klein et al. 2014) — first coordinated multi-site replication: some effects very robust, others not.

By 2014–15, “reproducibility crisis” is a live, contested label. What is the base rate of replication?

The Open Science Collaboration

  • Coordinated through the Center for Open Science (Brian Nosek, founded 2013, Charlottesville VA).
  • ~270 contributing authors, three years of work (2011–2015).
  • Goal: one large, pre-registered, transparent estimate of replicability in psychology, with open data, materials, and code on OSF (osf.io).
  • First project of its kind at this scale; template for later efforts:
    • Many Labs 2/3/5, Social Sciences Replication Project (SSRP, 2018),
    • Reproducibility Project: Cancer Biology (started 2013, results 2021).
  • Output: the present paper + a public registry of 100 replication reports.

Question and design

What did they ask?

What proportion of published psychology findings can be reproduced by independent teams using high-powered direct replications and the original materials?

  • Direct replication: same methods, new sample. Not conceptual replication.
  • Five operational indicators of “did it replicate” (next slide).
  • Single point estimates are dangerous — they report multiple complementary indicators because no single number captures replication.

Study selection

  • Source: 2008 issues of three journals
    • Psychological Science (PSCI) — general
    • Journal of Personality and Social Psychology (JPSP) — social
    • Journal of Experimental Psychology: Learning, Memory & Cognition (JEP:LMC) — cognitive
  • Within-journal sampling: articles ordered chronologically from the first 2008 issue forward; 488 articles in the frame, 158 (≈32%) became eligible. Replication teams self-matched to articles by expertise from the available pool; coordinators also recruited teams for specific articles. Final pool sizes: PSCI 68, JPSP 59, JEP:LMC 40.
  • Within-article sampling: target the last reported effect — an objective rule, since first studies tend to be preliminary demonstrations.
  • Final set: 100 replications completed.
  • Each replication: pre-registered protocol, reviewed by original authors when possible, high statistical power (median ~92%).

Five success criteria

# Indicator Question it answers
1 Replication p < .05, same direction Did the replication itself reject the null?
2 Original effect inside replication 95% CI Is the original estimate compatible with the replication?
3 Replication effect size vs original How much smaller (or larger) is the new estimate?
4 Meta-analytic combination of the two What is the pooled evidence?
5 Subjective “did it replicate?” rating Holistic judgement by the replicating team

No single number is privileged. This is a deliberate methodological stance.

Results

Significance rates

  • 97% of original studies reported p < .05.
  • 36% of replications reached p < .05 in the same direction.
  • 47% of replication effects fell inside the original 95% CI.
  • 39% were subjectively judged to have replicated.
  • Pooled (original + replication) meta-analysis: 68% of combined intervals exclude zero — but this conflates original and new evidence.

Whichever indicator you pick, the rate is substantially below what the published literature would suggest.

Fig. 1 — distributions of p values and effect sizes

Density plots of original and replication p-values and effect sizes

Fig. 2 — original vs replication p values

Scatterplot of original vs replication p-values, by journal

Fig. 3 — original vs replication effect sizes

Scatterplot of original vs replication effect sizes, with marginal densities

Moderators of replication success

Replication was more likely when:

  • Original p value smaller — far more predictive than reaching .05.
  • Original effect size larger.
  • Original study rated less “surprising” by the replicating team.
  • Cognitive > social psychology (≈50% vs ≈25% by the p < .05 criterion).
  • Field, journal, and study characteristics matter; individual replication teams’ effort did not predict outcomes much.

Implication: p just under .05 is weaker evidence than the field treats it as.

Discussion

How should we read this?

  • Non-replication ≠ falsification. A single failed replication is just another single study.
  • Original effects are likely inflated by publication selection and flexibility in analysis (winner’s curse).
  • Replicability is necessary but not sufficient for truth — a finding can be replicable and still wrong (e.g. confounded).
  • The honest summary is uncertainty, not a verdict on any one finding.

Critiques and the back-and-forth

  • Gilbert, King, Pettigrew & Wilson (2016, Science) challenged the headline number, arguing
    • protocol infidelities (different populations, materials) lowered replication rates,
    • the 36% figure understates the “true” replicability,
    • sampling within journal issues was non-random.
  • OSC reply (Anderson et al. 2016): defended the design, noted that the critique itself relied on selective use of indicators and assumed perfect original-study fidelity.
  • Broader point: any single summary statistic is contestable; the value of the project is the open dataset, not the headline.

Implications for practice

  • Single studies are weak evidence, even when p < .05.
  • Pre-registration, larger samples, open data and materials should be defaults.
  • Direct replications deserve publication and credit.
  • Cumulative evidence (meta-analysis, registered replication reports) over hero studies.
  • This paper helped catalyse: TOP guidelines, Registered Reports, mandatory data-sharing policies, and the broader Open Science movement.

Questions for the room

Discussion

  1. How much of the gap is publication bias vs questionable research practices vs genuine heterogeneity across samples and contexts?
  2. Are the same dynamics at work in your field? (statistics, biostatistics, oncology, …)
  3. How would a Bayesian account of these data differ — prior plausibility, posterior probability of an effect?
  4. Where does direct replication stop being informative and theoretical reformulation start?

References

  • Open Science Collaboration (2015). Estimating the reproducibility of psychological science. Science 349: aac4716. doi:10.1126/science.aac4716
  • Ioannidis JPA (2005). Why most published research findings are false. PLoS Med 2: e124.
  • Simmons JP, Nelson LD, Simonsohn U (2011). False-positive psychology. Psychol Sci 22: 1359–66.
  • Klein RA et al. (2014). Investigating variation in replicability: a “Many Labs” replication project. Soc Psychol 45: 142–52.
  • Gilbert DT, King G, Pettigrew S, Wilson TD (2016). Comment on “Estimating the reproducibility of psychological science.” Science 351: 1037.
  • Anderson CJ et al. (2016). Response to Comment on … Science 351: 1037.
  • Gambarota, Fitelson, Parmigiani (2025). The Three Rs of Trustworthy Science. https://filippogambarota.github.io/replicability-book/

Backup slides

Ioannidis (2005)

“Why most published research findings are false”PLoS Medicine.

  • Treats research findings as a screening test. Positive predictive value depends on:
    • Prior odds R of a true relationship in the field
    • Power 1 − β of the study
    • Bias u (flexibility, selective reporting)
  • PPV = (1 − β)R / (R + α − βR + u(1 − β + βR))
  • With low prior odds (exploratory hypotheses) and low power (small N), most “significant” findings are false.
  • Bias can be modelled and dominates as it grows; small studies with extreme flexibility have PPV near zero.
  • Foundational reference for the field-level pessimism that the OSC project tests empirically.

Bem (2011) — precognition in JPSP

“Feeling the future” — nine experiments, 1,000+ participants, claimed evidence that future events influence past responses.

  • Used standard JPSP-acceptable methods: that is the point.
  • Wagenmakers, Wetzels, Borsboom & van der Maas (2011) Bayesian re-analysis: same data, Bayes factors strongly favour the null.
  • Galak, LeBoeuf, Nelson & Simmons (2012) ran direct replications across seven studies, N > 3,000: no effect.
  • Ritchie, Wiseman & French (2012): three further failed replications, initially rejected by JPSP.
  • Crystallised the question: if standard methods can deliver “evidence” for precognition, what else are they delivering?

Simmons, Nelson & Simonsohn (2011)

“False-positive psychology”Psychological Science.

  • Quantified researcher degrees of freedom: optional stopping, selective reporting of conditions/measures, covariate inclusion, transformations.
  • A simulation and a real experiment showed Type-I error can reach ~60% with four such choices undisclosed.
  • Coined the “garden of forking paths” intuition (later formalised by Gelman & Loken 2013).
  • Six author requirements + four reviewer guidelines — including: justify N a priori, list all conditions, report all variables, all exclusions.
  • Direct intellectual ancestor of pre-registration and Registered Reports.

Stapel (2011) — fraud

Diederik Stapel, social psychologist at Tilburg, suspended after PhD students raised the alarm.

  • ~58 retractions by 2015, including high-profile Science papers (e.g. on disorder priming racial stereotyping).
  • Levelt, Noort & Drenth Commission (2012) report: years of outright data fabrication, undetected by co-authors, reviewers, editors.
  • The point is not that fraud is the cause of the crisis — it is rare. Stapel made fabrication indistinguishable from normal practice until students checked. That diagnosis was the wake-up.
  • Catalysed Dutch and broader policy on data archiving and verification.

Doyen et al. (2012) — elderly priming

Direct replication of Bargh, Chen & Burrows (1996): priming “elderly” stereotypes claimed to slow participants’ walking speed leaving the lab.

  • Doyen et al. ran two experiments (Brussels) with infrared timing instead of stopwatch.
  • No effect of prime on walking speed when experimenters were blind to condition.
  • Effect appeared when experimenters knew the condition — consistent with experimenter expectancy, not unconscious priming.
  • John Bargh’s combative blog response amplified the controversy and drew the wider community in.
  • Part of a broader wave of failures for social priming effects (money priming, professor priming, etc.).

Many Labs 1 — Klein et al. (2014)

First large coordinated replication: 36 sites, 6,344 participants, 13 classic effects.

  • Each site ran the same standardised protocol on its local sample.
  • 10 of 13 effects replicated in the expected direction; some very robustly (anchoring), others not at all (currency priming, flag priming).
  • Heterogeneity across sites was small for most replicated effects: the variation people feared (culture, language) was less of a story than expected.
  • Demonstrated feasibility of coordinated, pre-registered, multi-site replication — directly inspired OSC and later Many Labs 2/3/5.