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Study identifier: NCT07382206 Synced from ClinicalTrials.gov · July 29, 2026
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Effect of Acute Exercise on Sleep Patterns in Patients With PLMS, Using a Wearable Device, Compared With a Control Group ( SONEX )

Condition: Periodic Leg Movements, Excessive, Sleep-Related  ·  Sponsor: Associação Fundo de Incentivo à Pesquisa

PhaseNA
Planned participants150
Who can joinAll sexes, 22 Years to no upper limit
Healthy volunteersYes

About this study

The effects of chronic exercise on health promotion, improvement of quality of life, and reduction of the risk of developing chronic diseases such as obesity, diabetes mellitus, cardiovascular diseases, depression, and cancer are well established. In addition, the positive influence of exercise on sleep patterns and sleep quality is widely recognized. However, few studies have addressed the effects of a single session of physical exercise on the circadian cycle and sleep disorders. Regarding Periodic Limb Movement Disorder (PLMD), which is characterized by periodic episodes of repetitive and highly stereotyped limb movements, the scientific literature indicates that the effects of a single session of intense exercise remain insufficiently explored. Therefore, the present study aims to investigate, through a controlled interventional study, the effects of acute exercise on the Periodic Limb Movements of Sleep (PLMS) index. To this end, the study will recruit healthy participants as well as individuals with PLMS to perform acute exercise sessions, followed by a polysomnographic examination and a longitudinal observation period. Throughout the study, participants will use wearable and mobile devices to monitor their physiological patterns. In addition, questionnaires related to sleep, physical exercise, cognitive decline, and depression will be administered to better characterize the study population. Thus, this study aims to generate evidence regarding the influence of acute…

This description comes directly from the study's public registry record.

Talk to the study team

Magda Bignotto, PhD  ·  5511971547331  ·  magda.bignotto@cdecbrasil.com.br

Suelen Oliveira da Rosa, BPharm  ·  551155790373  ·  suelen.rosa@cdecbrasil.com.br

Always discuss trial participation with your own doctor first.

Locations (1)

CDEC BrasilSão Paulo, São Paulo, BrazilRecruiting

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Source record: clinicaltrials.gov/study/NCT07382206