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Creatine supplementation effects on cognition, sleep, and menopause symptoms in response to six weeks of high-intensity resistance training in perimenopausal females.

Created on 25 Oct 2026

Authors

Paul A Baker, Gabrielle M DelBiondo, Caroline G Kelly, William M Johnson, Gregory J Grosicki, Abbie E Smith-Ryan

Published in

European journal of applied physiology. Oct 24, 2026. Epub Oct 24, 2026.

Abstract

Perimenopause (PERI) women experience cognitive dysfunction, sleep disturbances, and menopause-related symptoms, yet few accessible and time-efficient interventions have been evaluated. The purpose of the current study was to determine the impact of creatine monohydrate (CM) during six weeks of high-intensity resistance training (HIRT) on cognition, sleep, and menopause symptoms in PERI females.
PERI females (n = 51; Age: 46 ± 5 yrs) were randomized to CM (n = 18), placebo (PLA) (n = 20), or a non-training control (CON) group (n = 13). CM and PLA groups completed a 5-day loading phase (20 g·day⁻¹) followed by six weeks of maintenance (~ 4.5 g·day⁻¹) combined with twice-weekly progressive HIRT. Cognitive performance (Stroop, Rey 15-item memory test) and prefrontal oxygenation via functional near-infrared spectroscopy were assessed at baseline (BASE), pre- (PRE), and post-training (POST). Sleep and self-reported menopause symptoms (temperature sensitivity, fatigue, soreness, brain fog, and bloating) were monitored daily using a WHOOP wearable wristband.
Stroop reaction time improved over time (congruent: p < 0.001; incongruent: p = 0.004) with no group differences. Prefrontal oxygenation during the Stroop test increased with CM at POST (+ 0.32 ± 2.01%) compared to a decrease with PLA (- 1.62 ± 2.01%; p = 0.003). Sleep consistency showed a time × treatment interaction (p < 0.001), with higher consistency in CM than PLA at week 6 (baseline-adjusted mean difference: +7.4% points, p = 0.015).
In this exploratory analysis, CM combined with HIRT was associated with greater prefrontal oxygenation, higher sleep consistency, and fewer self-reported temperature sensitivity days relative to PLA in PERI females.

PMID:
42926218
Bibliographic data and abstract were imported from PubMed on 25 Oct 2026.

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