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Recruiting NCT06967714

NCT06967714 Disentangling the Variability of Exercise-induced Hypoalgesia: the Role of Circulatory Compounds

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Clinical Trial Summary
NCT ID NCT06967714
Status Recruiting
Phase
Sponsor Université Catholique de Louvain
Condition Healthy
Study Type INTERVENTIONAL
Enrollment 90 participants
Start Date 2025-04-14
Primary Completion 2026-04-01

Trial Parameters

Condition Healthy
Sponsor Université Catholique de Louvain
Study Type INTERVENTIONAL
Phase N/A
Enrollment 90
Sex ALL
Min Age 18 Years
Max Age 30 Years
Start Date 2025-04-14
Completion 2026-04-01
Interventions
Exercise

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Brief Summary

Physical exercise is increasingly recognized as an effective treatment for chronic pain. Studies in humans and animals have shown that a single session of exercise induces a reduction of sensitivity to experimental painful stimuli lasting up to 45 minutes. In a recent study conducted in our laboratory, we found (1) that this exercise- induced hypoalgesia (EIH) is mainly driven by local changes in muscle nociceptor sensitivity within exercising muscles and (2) that EIH is consistent at a group level but fluctuates across sessions within participants. The first aim of this project is to uncover the mechanism(s) that drive EIH by investigating whether processes that could contribute to an exercise-induced change in muscle nociceptor sensitivity match the fluctuating pattern of EIH. Specifically, we will assess the possible involvement in EIH of the endocannabinoid system (eCB), Kynurenic acid (KynA, a circulating myokine that transiently increases after exercise), and β -endorphins (βE). Using a sample of 90 healthy males and females aged 18 to 30 years, we will measure sensitivity to blunt pressure stimuli before, immediately after, and 45 min after a 25-min cycling exercise to assess muscle nociceptor sensitivity at exercising (rectus femoris muscle) and non-exercising (ventral forearm) muscles. Blood samples will be collected at these time-points to measure plasma levels of eCBs, βE, and KynA. In addition, the effect of sex on EIH is controversial: some studies report no differences between males and females, while others report a greater effect in males or in females. Therefore, a secondary aim of this study is to explore potential sex differences in the manifestation and underlying mechanism(s) of EIH.

Eligibility Criteria

Inclusion Criteria: * Males, or females using hormonal contraception since ≥ 3 months. * Aged between 18 and 30 years. * Ability to provide written informed consent. * Fluency in French or English. * BMI between 17 and 30 kg/cm2. Exclusion Criteria: * Regular tobacco use (\> 1/month) * Not willing or able to abstain from alcohol, recreational drugs, coffee, or tea from 24 hours prior to each experimental session. * Not willing or able to restrain from physical activity \> 24h prior to each experimental session, and to be in a fasted state on the day of each experimental session. * Any evidence for neurological, cardiovascular, respiratory, inflammatory, endocrine, psychiatric, oncological, rheumatological conditions on direct questioning. * Presence of any medical devices (e.g., cardiac pacemaker) implants or prothesis unless it is beyond discussion that these will not put the subject's safety during the study at risk and will not interfere with the results of the study. * Any chronic

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