Metabolic, Functional and Nutritional Responses to Weight Cycling in Athletes: The WAVE Study (WAVE)

  • STATUS
    Recruiting
  • End date
    May 14, 2024
  • participants needed
    48
  • sponsor
    University Hospital, Clermont-Ferrand
Updated on 14 June 2022
Accepts healthy volunteers

Summary

Many elite athletes are submitted to frequent rapid weight loss periods to meet their competition weight category and then experience weight cycling (lowing and gaining weight regularly). This weight cycling induce severe temporary energetic and metabolic changes and when repeated over time can lead to permanent metabolic adaptations that might favor metabolic disorders, body weight gain and body composition changes (favoring fat mass). The exact effects of this weight cycling are not clear yet, especially in terms of metabolic, energetics, nutritional functional and psychological impacts. Better understand these adaptations and their variations during weight loss and weight gain in regular weight cycler is of main importance to prevent these athletes for future health issues.

The aim of the present project if to assess these metabolic, functional, energetic and nutritional adaptations during weight loss, weight stable and weight gain periods in athletes experiencing regular weight cycling.

Description

After an inclusion visit to ensure the eligibility of athletes to complete the entire study, each subject will perform 3 experimental sessions of 2 visits each : i) two visits during a period of maintenance of body weight (CON); ii) two visits during weight loss (WL); iii) two visits during a weight regain (WG). The order of the periods (maintenance, loss or weight gain) will depend on the dynamics of the weight variations of each athlete (endurance sport and weight class) during the season and will therefore be individualized.

All experiments will be conducted in the same way for the CON, WL or WG session.

Upon arrival, each subject will perform a resting metabolism with continuous measurement of heart rate variability (≈ 30 min). Then, from 8:30, blood and saliva samples will be taken (≈ 10 min). Then (≈ 8:45), they will perform anthropometric and body composition measurements (waist circumference, hip circumference, bioimpedance, DXA) (≈ 30 min). Following these measurements (≈ 9:15), the subjects will eat a standardized breakfast and the report to food will be evaluated thanks to the Leeds Foods Preference Questionnaire before and after the meal. They will then be asked (≈ 10h) to complete the Profile of Mood State Questionnaire to measure the athlete's psychological state. Participants will then perform a measurement of muscle function (≈ 10:30).

During the second visit, carried out between 1 and 5 days after the first visit, the maximum aerobic capacity of the athletes will be evaluated by mid-morning stress test.

Details
Condition Athletes
Treatment athletes, athletes
Clinical Study IdentifierNCT04107545
SponsorUniversity Hospital, Clermont-Ferrand
Last Modified on14 June 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Subjects aged 18 to 35 (inclusive)
exercising at least 4 sessions of endurance or weight-based sporting activities per week for a performance objective
having variations of at least 5% of their weight body during the last 3 sporting seasons (a sporting season corresponds to a year during which alternates the periods of training, recovery and participation in official competitions)
Subject capable of providing informed consent to participate
Subject with a social security insurance

Exclusion Criteria

Medical or surgical history deemed by the investigator to be incompatible with the study
Presence of chronic pathology
Disorders of eating behavior
Subjects born very prematurely defined as a pregnancy inferior to 28 weeks
Subjects having used a treatment for a small stature (eg growth hormone)
For women: irregular menstruation (changes in menstrual cycles ≥ 6 days)
Sports subjects with a stable weight during the last three sporting seasons (weight variation <5%)
Take medication that can change body temperature
Pregnant or lactating women
Subjects with gastrointestinal complications and / or contraindications to ingestion of the capsule (eg diverticulosis, inflammatory bowel disease, gastrointestinal surgery ...)
Subjects needing MRI during ingestion of the capsule or having a pacemaker or other implanted electro-medical device
Person under guardianship or not subject to a social security scheme
Refusal to sign the information and consent leaflet
Refusal of participation
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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