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Eight‐Week Minimal Dose Training Reduces Premenstrual Syndrome Symptoms but Does Not Influence Coping Strategies

A Nonrandomized Study

Bibliographic Data

ID21391867
AuthorsEliane Aragão da Silva Soares (0000-0002-9498-9707, Human Movement Sciences Graduation Program Universidade Federal do Pará (UFPA) Castanhal Pará Brazil, corresponding author), Alex Harley Crisp (0000-0003-4683-9576, Human Movement Sciences Graduation Program Universidade Federal do Pará (UFPA) Castanhal Pará Brazil), Paula Teixeira Fernandes (0000-0002-0492-1670, Physical Education Graduation Program Universidade Estadual de Campinas (UNICAMP) Campinas São Paulo Brazil), Eduardo Macedo Penna (0000-0003-0058-7967, Human Movement Sciences Graduation Program Universidade Federal do Pará (UFPA) Castanhal Pará Brazil), Daniel Alves Pires (0000-0003-2163-5606, Human Movement Sciences Graduation Program Universidade Federal do Pará (UFPA) Castanhal Pará Brazil, corresponding author)
Year2026
Publication date2026-06-23
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueScandinavian Journal of Psychology (JOURNAL)
Journal identifiersISSN: 0036-5564 • E-ISSN: 1467-9450
PublisherWiley (PUBLISHER • GB)
DOI10.1111/sjop.70125
PMID42334229
OpenAlexW7165637821
LanguageEN
References cited41

Premenstrual syndrome (PMS) is a set of symptoms related to hormonal changes occurring during the premenstrual period. Effective coping strategies for managing PMS have not been clearly established, and it remains unclear whether these strategies are modified by physical activity. Exercise may reduce PMS symptoms; however, the minimum effective exercise dose remains unknown. This study aimed to analyze the effects of an 8‐week minimum‐dose exercise protocol on psychological PMS symptoms and coping strategies. Thirty‐three university students with PMS were assigned to two groups: the Resistance Training Group (RTG), which followed an 8‐week minimum‐dose training protocol, and the Control Group (CG), which underwent only physical testing. The Premenstrual Symptom Screening Tool (PSST) and the Brief COPE were used for assessments. A mixed linear model with Restricted Maximum Likelihood (REML), ANOVA III table application, and Tukey's post hoc test was used for PMS analysis. For coping strategies, a mixed linear model was applied to each domain, with descriptive and exploratory analyses. These analyses were performed in R Studio. For the physical tests, the mean and standard deviation of the variables in each group at the three protocol time points were calculated, and differences between groups were analyzed using Student's t ‐test conducted in Jamovi. A reduction in both physical and psychological PMS symptoms ( χ 2 = 7.64, df = 2, p = 0.02) and functional impacts ( χ 2 = 6.37, df = 2, p = 0.04) was observed in the RTG compared to the CG during the second evaluation. Coping strategy patterns remained stable, showing no influence from the minimum‐dose protocol. The minimum‐dose exercise approach effectively reduced PMS symptom severity and functional impairments but did not affect coping strategies. Trial Registration: Brazilian Clinical Trials Registry (ReBEC) number: RBR‐4pp65c6

Analysis of variance · Coping (psychology) · Descriptive statistics · Exploratory research · Post-hoc analysis · Randomized controlled trial · Repeated measures design · Biofield Effects and Biophysics · Exercise and Physiological Responses · Menstrual Health and Disorders

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