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Study identifier: NCT06746220 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effect of Physical Activity and/or Probiotics on Body Composition and Physiological Parameters in Women

Condition: Healthy Women  ·  Sponsor: Centre Hospitalier Régional d'Orléans

PhaseNA
Planned participants120
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersYes

About this study

This is a prospective, comparative, double-blind, randomized, monocentric study. The objective of this project is to evaluate the effects on health of probiotic supplementation (PS) with or without physical activity (PA). Participants who meet the study criteria will be randomized into 4 groups: probiotic and physical activity group (A+), probiotic and non-physical activity group (A-), placebo and physical activity group (T+), placebo and non-physical activity group (T-). The probiotics used are Lactibiane® Reference provided by Pileje Laboratory. The study population are healthy women (university students) who do not practice sports. A total of 120 participants will participate. At inclusion, each participant will undergo a medical examination, collect microbiota and salivary samples and perform different tests (questionnaires, assessments of strength and endurance). Then, a follow up phase will last 6 weeks. Each participant will receive a pillbox containing capsules (probiotic or placebo in a double-blind manner). Participants which randomized in the PA groups (A+ and A-) will perform 2 physical activity sessions per week for 6 weeks. At the end of this follow up phase, tests conducting during inclusion will be performed again.

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

Talk to the study team

Virgile AMIOT, Doctor  ·  0238514785  ·  virgile.amiot@chu-orleans.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Center Hospitalier Universitaire d'OrléansOrléans, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06746220