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What effect sizes can we expect in functional neuroimaging?
Poster Session A - Saturday, March 7, 3:00 – 5:00 pm, Fairview/Kitsilano Ballrooms
Hallee Shearer1, Matt Rosenblatt2, Jean Ye2, Rongtao Jiang2, Link Tejavibulya2, Maya Foster2, Qinghao Liang2, Javid Dadashkarimi3, Margaret Westwater2, Iris Cheng2, Max Rolison7, Hannah Peterson2, Brendan Adkinson2, Saloni Mehta2, Chris Camp2, Alexandra Fischbach1, Fabricio Cravo1, Amanda Meija4, Thomas Nichols5, Joshua Curtiss1,6, Dustin Scheinost2,7, Stephanie Noble1,2; 1Northeastern University, 2Yale University, 3University of Pennsylvania, 4Indiana University, 5University of Oxford, 6Massachusetts General Hospital, 7Yale School of Medicine
Emerging reports suggest that sample sizes commonly used in functional neuroimaging studies may be too small to detect many brain-behavior relationships, posing a major barrier to progress in brain and mental health research. Determining adequate sample sizes requires knowledge of what effect sizes to expect a priori, yet this is notoriously difficult to estimate in practice, leading researchers to rely on ad hoc assumptions and study planning procedures. To address this problem, we performed 63 effect size analyses in seven large, publicly available datasets (n = 100–40,000; 52,979 total participants) to obtain effect size estimates for ‘typical’ fMRI study designs. These included brain-behavior correlations, one-sample t-tests, two-sample t-tests, and multivariate versions of each test for functional connectivity and task-based activation maps. We then developed a principled approach to estimate the “true” population effect size distributions across the brain for these common fMRI study designs. We found that between-subject effects were exceedingly small at the majority of brain areas, requiring sample sizes beyond typical consortia (n > 5,000; 80% power) to detect even the largest voxel- or edge-level effects. However, multivariate analyses and within-subject task designs yielded substantially larger effect sizes that can be detected at sample sizes within reach of most labs (n < 25–50). By establishing data-driven effect size benchmarks, these findings lay the groundwork for more informed study planning in neuroscience and further contextualize shared challenges facing high-dimensional biomedical research.
Topic Area: METHODS: Neuroimaging
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March 7 – 10, 2026