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Clinical Trials/NCT05028959
NCT05028959
Not yet recruiting
Not Applicable

Menstrual Cycle, Amenorrhea and Contraception in Elite Female Athletes: Impact on Performance, Health and the Athlete's Biological Passport

Université Paris-Saclay-Assistance publique des hôpitaux de Paris0 sites80 target enrollmentSeptember 15, 2021
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
Université Paris-Saclay-Assistance publique des hôpitaux de Paris
Enrollment
80
Primary Endpoint
Change from baseline metabolic parameters
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

The repercussions of the hormonal status of high-level sportswomen on their performance and health as well as on the Athlete's Biological Passport (ABP) have been little studied and remain poorly known. The investigators therefore propose to contribute to the improvement of current knowledge by determining, thanks to the implementation of a multidisciplinary monitoring, with the use of various tests and matrices, in female elite athletes and recreational athletes (control group):

    1. the impact of cycle phase, absence of cycle or contraceptive use on physical and psychological performance, health as well as on ABP;
    1. the potential confounding effects of the athlete's environment
    1. correlations between the different matrices analyzed

Detailed Description

Volunteers to be studied: 80 healthy female subjects (16 to 30 years old), divided into 2 groups: Group 1: 60 athletes, from different sports disciplines, in amenorrhea, with menstrual cycle or taking contraceptives Group 2: 20 leisure sports subjects with menstrual cycle or taking contraceptives Following the oral and written information of the project, the subjects have a minimum of 15 days of reflection before signing the written consent form. They will have the possibility, at any time, to voluntarily interrupt the study without having to justify themselves. Investigations to be performed: 1. Annual complete clinical examination : 2. "Out-of-competition" follow-up, time frame 6 months * medical, nutritional and respiratory monitoring * biological monitoring * psychological monitoring * performance monitoring 3. Non-invasive "in-competition" monitoring, only for Group 1, once in a year on the day before/after a major competition: * biological monitoring * psychological monitoring * performance monitoring (interview)

Registry
clinicaltrials.gov
Start Date
September 15, 2021
End Date
May 31, 2025
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Université Paris-Saclay-Assistance publique des hôpitaux de Paris
Responsible Party
Principal Investigator
Principal Investigator

Emmanuelle Duron

Head of Geriatry, Principal investigator

Université Paris-Saclay-Assistance publique des hôpitaux de Paris

Eligibility Criteria

Inclusion Criteria

  • Group 1: high-level athletes (qualified for national/international championships and/or training at least 15 hours/week)
  • Group 2: recreational athletes who practice a regular physical activity

Exclusion Criteria

  • Participation in another trial
  • History of cardiac pathology
  • High blood pressure
  • History of ulcers and other gastrointestinal disorders
  • Myasthenia
  • Renal insufficiency
  • Person not affiliated or not benefiting from a social security system

Outcomes

Primary Outcomes

Change from baseline metabolic parameters

Time Frame: 6 months

concentration of blood glucose, blood lactate, lipid profile, insulin, GH, IGF1, T3, IgA, PRL and leptin in mol/L

Change from baseline weight

Time Frame: 6 months

in kg, by impedancemeter

Change from baseline fat and lean mass

Time Frame: 6 months

in kg, by impedancemeter

Change from baseline height

Time Frame: 6 months

in cm, by height gauge

Change from baseline sex and stress hormones

Time Frame: 6 months

concentration of oestradiol, progesterone, testosterone, DHEA, cortisol, LH and FSH in mol/L

Change from baseline food intake

Time Frame: 6 months

food intake questionnaire to complete over 3 days, expressed in kcal/day

Change from baseline inflammatory parameters

Time Frame: 6 months

concentration of cytokines (TNF-alpha, IL-6) in mol/L

Change from baseline executive function

Time Frame: 6 months

assessed by instability via static and dynamic postures (eyes open/closed) on platform

Change from baseline visual-spatial processing

Time Frame: 6 months

3 D mental rotation test, assessed by scores: range from 0 - 24, with 24 representing a perfect total score

Change from baseline attention and working memory

Time Frame: 6 months

Stroop Color Word Task, assessed by scores : range of interference from -15 - +15, with higher scores representing decreased selective attention

Change from baseline performance monitoring

Time Frame: 6 months

field performance test, performance expressed in time

Change from baseline Athlete Biological Passport (Group 2)

Time Frame: 6 months

assessed by analysis of the standardized parameters of the Athlete Biological Passport (WADA)

Change from baseline respiratory parameters

Time Frame: 6 months

measure of FEV1 (forced expiratory volume in 1 second), expressed in % of vital capacity

Change from baseline affects (Group 2)

Time Frame: 6 months

Positive Affect and Negative Affect Schedule (PANAS), assessed by scores. Positive Affect Score: range from 10 - 50, with higher scores representing higher levels of positive affect. Negative Affect Score: range from 10 - 50, with lower scores representing lower levels of negative affect.

Change from baseline anxiety (Group 2)

Time Frame: 6 months

Spielberger State-Trait Anxiety Inventory, assessed by scores: range from 20 - 80, with higher scores representing higher anxiety

Change from baseline Athlete Biological Passport (Group 1)

Time Frame: 8 months

assessed by analysis of the standardized parameters of the Athlete Biological Passport (WADA)

Change from baseline affects (Group 1)

Time Frame: 8 months

Positive Affect and Negative Affect Schedule (PANAS), assessed by scores. Positive Affect Score: range from 10 - 50, with higher scores representing higher levels of positive affect. Negative Affect Score: range from 10 - 50, with lower scores representing lower levels of negative affect.

Change from baseline anxiety (Group 1)

Time Frame: 8 months

Spielberger State-Trait Anxiety Inventory, assessed by scores: range from 20 - 80, with higher scores representing higher anxiety

Interview (Group 1)

Time Frame: 8 months

Self-confrontation interview for questioning the action

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