The claim under review
Brief expansive poses reliably increase testosterone, decrease cortisol and increase risk tolerance relative to contractive poses.
Claim summary, not a verbatim quotation.
Our assessment
Not robustly supported
The original experiment
Carney, Cuddy and Yap randomly assigned 42 participants to expansive or contractive postures. Participants held two poses for one minute each, provided saliva samples, made a gambling choice and reported feelings of power. The paper concluded that pose condition changed testosterone, cortisol and risk tolerance, alongside subjective power. Random assignment was a useful design feature, but a small study can still produce unstable effect estimates. Our assessment concerns this specific endocrine-and-risk package, not whether posture can ever affect experience or communication. [1]
What the larger replication found
Ranehill and colleagues studied 200 participants with experimenters blind to pose condition. They did not find significant hormone or risk-taking effects, while reproducing an effect on self-reported power. This was a conceptual replication: pose duration and instructions differed. They also disclosed increasing the sample after the first 100 observations. These qualifications deserve attention, but they do not turn the absent endocrine results into confirmation. A subjective response is a different endpoint from a salivary hormone change or gambling behavior. [2]
Analytical fragility
Credé and Phillips reanalyzed the original results using plausible alternative choices about outliers, outcome specification and control variables. Their 2017 paper found hormone-effect conclusions highly sensitive to those choices. This is evidence about robustness, not proof of intent or a demonstration that a particular analyst knowingly selected a preferred answer. A persuasive result should not depend heavily on one defensible analysis when other reasonable analyses produce a different conclusion. That issue independently lowers the methods assessment, rather than merely counting a failed replication twice. [3]
The follow-up record is not uniformly null
Barel and colleagues' 2024 experiment enrolled 92 young adults. It did not reproduce the testosterone or felt-power findings, while reporting partial support involving cortisol and risk-taking. The distinction is important: its discussion describes an association between cortisol changes and risk-taking, while its main hormonal analysis did not find a significant time-by-pose effect for cortisol. An association within the follow-up analysis does not establish that the pose manipulation reliably caused the original hormone-and-behavior package. The authors themselves frame their findings cautiously. This review includes that mixed result rather than claiming every later experiment found nothing. [4]
Editorial judgment
Taken together, the selected evidence does not justify presenting a brief power pose as a dependable way to alter testosterone, suppress cortisol and raise risk tolerance. The low grade is attached to that conjunctive claim. It is not a judgment about any author's character, a diagnosis of misconduct, or a verdict on all research involving body posture. The appropriate uncertainty is narrower than either popular enthusiasm or a blanket dismissal: subjective effects and specific contextual effects need their own endpoints and evidence. This site did not collect new participants, recompute the datasets or conduct a systematic meta-analysis. The score records a reasoned assessment of the cited studies, with room for revision if stronger directly relevant evidence appears.
Documented problems & their consequences
The larger conceptual replication did not recover the original endocrine or risk-taking effects.
The 2010 result should not be presented as a robustly replicated hormone-and-behavior intervention; protocol differences remain a qualification.
Read the supporting source ↗A reanalysis found hormone conclusions sensitive to reasonable analytical specifications.
The original estimates provide weaker support than an analysis-insensitive result would. This finding does not establish intent.
Read the supporting source ↗How we reached the grade
Claim support 1/5 · 40% weight
The original package is not sustained by the larger replication; a 2024 study reports only limited, mixed support. [2, 4]
Methods & controls 2/5 · 20% weight
A small original experiment and sensitivity to analytical choices weaken confidence in the endocrine inference. [1, 3]
Independent checks 1/5 · 20% weight
The main hormone/risk result did not replicate in Ranehill; later mixed findings do not restore the whole claim. [2, 4]
Transparency 3/5 · 10% weight
Published methods and a later reanalysis permit scrutiny; the replication also released data and materials. This is not a complete audit of original materials. [2, 3]
Claim calibration 2/5 · 10% weight
The original practical causal interpretation was stronger than the selected follow-up evidence supports. [1–4]
What this review does not establish
Selected primary studies, not a complete systematic review. The grade is confined to the endocrine/risk claim and does not decide all subjective posture effects. Replication protocols differ; a nonsignificant result does not prove a mathematical zero effect.
The evidence over time
Original power-posing article published online.
Ranehill replication first published online, according to the publisher record.
Credé and Phillips publish the analytical-robustness reanalysis.
Barel and colleagues publish a follow-up with mixed endocrine results.
Primary sources & further evidence
- Original power-posing experiment · Carney, Cuddy and Yap, 2010 ↗
Primary experiment. Full text also verified through the publisher's accessible article view.
- Larger conceptual replication · Ranehill et al., 2015 ↗
Primary replication, N = 200. Full paper verified at faculty.haas.berkeley.edu/dana_carney/ranehill.pdf; data/materials linked by publisher.
- Original-data reanalysis · Credé and Phillips, 2017 ↗
Primary multiverse analysis of analytical choices; not an accusation of misconduct.
- Mixed endocrine follow-up · Barel et al., 2024 ↗
Primary N = 92 study; mixed results distinguish cortisol–risk associations from a replicated causal package.
Evidence can change a grade.
Point us to a factual error, a new replication, or a missing source. Authors can submit a response through the same process.
Submit a correction or response ↗