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Study identifier: NCT05123963 Synced from ClinicalTrials.gov · July 28, 2026
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Restoring 24-hour Substrate Rhythmicity to Improve Glycemic Control by Timing of Lifestyle Factors

Condition: Prediabetic State  ·  Sponsor: Université de Sherbrooke

PhaseNA
Planned participants48
Who can joinAll sexes, 45 Years to 75 Years
Healthy volunteersNo

About this study

Exercise is well-known to improve skeletal muscle energy metabolism and is an established intervention to improve muscle insulin sensitivity and to counter the development of type 2 diabetes (T2D). However, given the 24h rhythmicity in substrate metabolism previously observed in healthy, lean men and the lack of such rhythmicity in men with insulin-resistance, the investigator hypothesize that appropriate timing of exercise training can maximize the metabolic health effects of exercise. Indeed, a preliminary study in humans revealed that afternoon high-intensity interval training (HIIT) exercise was more effective than morning exercise in improving 24h blood glucose levels in men with T2D. Another recent study in mice showed that the time of day is a critical factor in augmenting the beneficial effects of exercise on the skeletal muscle metabolome as well as on whole-body energy homeostasis. However, human studies that specifically target the impact of timing of exercise training on glucose homeostasis and metabolic health are scarce and the potential underlying mechanisms largely unknown. The overarching goals of this project is to improve 24-hour rhythmicity of metabolism in men and women with prediabtes by appropriate timing of exercise and to assess its effect on metabolic health and immune response. Acute and prolonged exercise interventions timed in the morning vs late afternoon will be carried out in individuals with prediabetes to determine whether acute exercise in …

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

Talk to the study team

Frédérique Frisch  ·  819-346-1110  ·  frederique.frisch@usherbrooke.ca

Always discuss trial participation with your own doctor first.

Locations (1)

Centre de recherche du CHUSSherbrooke, Quebec, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT05123963