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Influence of Menstrual Cycle Stages on Female Athletes

U

Universitat Jaume I

Status

Completed

Conditions

Sports
Menstrual Cycle

Treatments

Other: Checking for correct use of contraceptive methods
Device: Sensory and pain threshold determination
Device: Daily activity
Procedure: Jump height determination
Procedure: Biochemical parameters determination
Procedure: Blood count determination
Procedure: Grip strength determination
Procedure: Vital signs
Other: Physical and mental symptoms associated with the menstrual cycle
Procedure: Determination of hormone level concentrations
Procedure: Flexibility determination
Procedure: Body composition parameters determination
Procedure: Indirect maximum oxygen consumption determination
Procedure: Urinary LH determination

Study type

Observational

Funder types

Other

Identifiers

NCT05576740
CD/77/2020

Details and patient eligibility

About

The influence of the menstrual cycle on women's sports performance is still uncertain. Research on this topic shows methodological biases. The aim of the study will be to determine whether the menstrual cycle affects women's physical fitness, measuring this in 3 differentiated stages of the cycle: the early follicular phase, late follicular phase, and luteal phase. For this purpose, a blood test will be carried out in each phase, with hormone determination (oestradiol and progesterone) and a haemogram to determine the existence of possible anemia. After the extraction and other complementary tests (measurement of vital signs, bioimpedance...) the woman will undergo 3 physical tests to compare the results in the 3 phases. A group of women taking hormonal contraception will also be included, performing the same interventions. To determine whether the woman is ovulating or not, urinary luteinizing hormone (LH) strips will be given to the women and they will have to take them from day 8 of the cycle. In addition, women will wear an accelerometer to monitor their daily activity and to be able to observe if there is an influence on this stage of the menstrual cycle.

Enrollment

41 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Inclusion criteria natural cycles group:

  • Female sex
  • Women between 18 and 40 years of age
  • Women who are members of a federation and who compete in a sport doing at least 240 minutes of exercise per week.
  • Women with regular menstrual cycles (between 23 and 38 days long).
  • Women who have not taken hormonal contraceptives (HA) for 6 months or more.

Inclusion criteria artificial cycles group:

  • Female sex
  • Women between 18-40 years of age
  • Women federated and competed in a sport doing at least 240 minutes of exercise per week.
  • Long-term users of HA (minimum 6 months).

Exclusion criteria

Exclusion criteria group natural cycles:

  • Refusal to participate in the study
  • Sedentary women
  • Women on HA currently or in the 6 months before the study
  • Women with irregular menstrual cycles, less than 23 or more than 38 days in length
  • Any existing metabolic disease or disorder
  • Regular use of medications or dietary supplements that could affect the results
  • Pregnancy or breastfeeding

Exclusion criteria artificial cycles group:

  • Refusal to participate in the study
  • Sedentary women
  • Any existing metabolic disease or disorder
  • Regular use of medications or dietary supplements that could affect the results
  • Inability to manage contraception in a disciplined manner

Trial design

41 participants in 3 patient groups

natural cycle
Description:
In this group, women have a natural menstrual cycle, not intervened by exogenous hormones. The interventions performed in this group are the same as in the other groups.
Treatment:
Device: Daily activity
Procedure: Flexibility determination
Procedure: Jump height determination
Procedure: Body composition parameters determination
Procedure: Vital signs
Procedure: Grip strength determination
Other: Physical and mental symptoms associated with the menstrual cycle
Procedure: Biochemical parameters determination
Device: Sensory and pain threshold determination
Procedure: Indirect maximum oxygen consumption determination
Procedure: Urinary LH determination
Procedure: Determination of hormone level concentrations
Procedure: Blood count determination
artificial cycle
Description:
In this group, women with an artificial menstrual cycle, i.e. women using hormonal contraception, oral or vaginal, are selected. The interventions carried out in this group are the same as in the other groups.
Treatment:
Device: Daily activity
Procedure: Flexibility determination
Procedure: Jump height determination
Procedure: Body composition parameters determination
Procedure: Vital signs
Procedure: Grip strength determination
Other: Physical and mental symptoms associated with the menstrual cycle
Procedure: Biochemical parameters determination
Other: Checking for correct use of contraceptive methods
Device: Sensory and pain threshold determination
Procedure: Indirect maximum oxygen consumption determination
Procedure: Determination of hormone level concentrations
Procedure: Blood count determination
natural cycle with deficient luteal phase
Description:
In this group, women have a natural menstrual cycle, with a low progesterone level during the luteal phase, and are not intervened by exogenous hormones. The interventions performed in this group are the same as in the other groups.
Treatment:
Device: Daily activity
Procedure: Flexibility determination
Procedure: Jump height determination
Procedure: Body composition parameters determination
Procedure: Vital signs
Procedure: Grip strength determination
Other: Physical and mental symptoms associated with the menstrual cycle
Procedure: Biochemical parameters determination
Device: Sensory and pain threshold determination
Procedure: Indirect maximum oxygen consumption determination
Procedure: Urinary LH determination
Procedure: Determination of hormone level concentrations
Procedure: Blood count determination

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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