ArticleThe international journal of biostatistics2021
Power formulas for mixed effects models with random slope and intercept comparing rate of change across groups.
Article in The international journal of biostatistics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Validation of a novel cognitive-functional outcome measure optimized for early Alzheimer's Disease: Evidence from the VIVA-MIND trial.The journal of prevention of Alzheimer's disease · 2026Trial
- Considerations for Using eGFR Slope as an End Point in Clinical Trials.Journal of the American Society of Nephrology : JASN · 2026Article
- Sample size determination for a study with variable follow-up time.Journal of biopharmaceutical statistics · 2025Article
- Power and Sample Size for Longitudinal Models in R - The longpower Package and Shiny App.The R journal · 2022Article
- Association of Neurofibrillary Tangle Distribution With Age at Onset-Related Clinical Heterogeneity in Alzheimer Disease: An Autopsy Study.Neurology · 2022Article
- A three-range approach enhances the prognostic utility of CSF biomarkers in Alzheimer's disease.Alzheimer's & dementia (New York, N. Y.) · 2022Article
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Abstract
We have previously derived power calculation formulas for cohort studies and clinical trials using the longitudinal mixed effects model with random slopes and intercepts to compare rate of change across groups [Ard & Edland, Power calculations for clinical trials in Alzheimer's disease. J Alzheim Dis 2011;21:369-77]. We here generalize these power formulas to accommodate 1) missing data due to study subject attrition common to longitudinal studies, 2) unequal sample size across groups, and 3) unequal variance parameters across groups. We demonstrate how these formulas can be used to power a future study even when the design of available pilot study data (i.e., number and interval between longitudinal observations) does not match the design of the planned future study. We demonstrate how differences in variance parameters across groups, typically overlooked in power calculations, can have a dramatic effect on statistical power. This is especially relevant to clinical trials, where changes over time in the treatment arm reflect background variability in progression observed in the placebo control arm plus variability in response to treatment, meaning that power calculations based only on the placebo arm covariance structure may be anticonservative. These more general power formulas are a useful resource for understanding the relative influence of these multiple factors on the efficiency of cohort studies and clinical trials, and for designing future trials under the random slopes and intercepts model.
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