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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05802277
Other study ID # 004B2022
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 5, 2022
Est. completion date April 1, 2024

Study information

Verified date February 2024
Source EZUS-LYON 1
Contact Melanie PRUDENT, MD
Phone 33472071862
Email melanie.prudent@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to precise the impact of menstrual cycle and physical activity on the hamstrings muscle function in healthy active women. The main question it aims to answer is : is there a moment of the menstrual cycle when the muscle is better able to recover from a strenuous exercise ? Three appointments will be conducted to evaluate the hamstring muscles at difference moments of the menstrual cycle. Echographic and maximal force production measures will be done. Researchers will compare these results with a group taking oral contraceptives.


Recruitment information / eligibility

Status Recruiting
Enrollment 130
Est. completion date April 1, 2024
Est. primary completion date April 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Subject aged between 18 and 35 years. - Subjects who practice at least 2 hours of sport per week with a competitive aim. - Subject who has not presented any musculo-tendinous pathology to the hamstrings in the last 6 months. - Subject with no musculoarticular pathology having a prolonged (more than 2 weeks) interruption of sports activities in the last 2 years. - Subject with no muscular pain or pathology currently. - Subject with no known cardiac disorders or family history that could present a risk known family history that could present a risk in case of intense physical effort. physical exertion. - Subjects not taking any medication, which in the opinion of the that, in the opinion of the coordinating investigator, may interfere with the evaluation of the study criteria. - Subject able and willing to comply with the protocol and agreeing to give written informed consent. - Subject affiliated or benefiting from a Social Security plan. Menstrual cycle group: - Subject whose last 3 menstrual cycles are of a regular duration (± 4 days maximum difference between 2 consecutive menstrual cycles). - Subject whose last 3 menstrual cycles are of a duration between 24 and 32 days (including milestones). - Absence of any contraceptive method likely to modulate the hormonal variations linked to the menstrual cycle. hormonal variations related to the menstrual cycle, during the duration of the duration of the protocol and during the last 6 months after the participant's inclusion. the participant. Mechanical contraception such as the diaphragm is permitted. Oral contraceptive group: - Taking oral contraception, 2nd generation monophasic pill estrogen-progestin pill (Optilova®, Optidril®, Leeloo®, Minidril®, Ludeal®, Zikiale®, Lovavulo®, Lovapharm®) for at least 6 months. Exclusion Criteria: - Subjects with a medical contraindication to intense physical activity. - Subject with a positive pregnancy test result. - Subject with a medical or surgical history deemed by the coordinating investigator as being incompatible with the study. - Subjects under guardianship. - Subjects in a period of exclusion from another study. - Decision of the volunteer, whatever the reason. - Adverse event or effect affecting the safety of the volunteer in the opinion of the coordinating investigator. - Major deviation from the protocol. - Illness or injury interfering with the normal course of the protocol.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Hamstring muscles function assessment
Ultrasound echographic evaluation of the hamstring muscles during stretching and voluntary contractions, before and after a strenuous physical activity.

Locations

Country Name City State
France Laboratoire Interuniversitaire de Biologie de la Motricité Villeurbanne Rhône

Sponsors (2)

Lead Sponsor Collaborator
EZUS-LYON 1 Laboratoire Interuniversitaire de Biologie de la Motricité

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hamstring muscles shear wave speed Differences according to menstrual cycle phase in hamstring muscles shear wave speed, as measured by ultrasound elastography Length of a menstrual cycle (around on 28 day average)
Secondary Maximal voluntary force production Differences according to menstrual cycle phase in maximal voluntary isometric hamstrings force production, as measured by an isokinetic dynamometer Length of a menstrual cycle (around on 28 day average)
Secondary Hamstring muscles thickness Differences according to menstrual cycle phase in hamstring muscles thickness, as measured by ultrasound echography. Length of a menstrual cycle (around on 28 day average)
Secondary Hamstring muscles length of fascicles Differences according to menstrual cycle phase in hamstring muscles fascicles' length, as measured by ultrasound echography. Length of a menstrual cycle (around on 28 day average)
Secondary Hamstring muscles pennation angle Differences according to menstrual cycle phase in hamstring muscles pennation angle, as measured by ultrasound echography. Length of a menstrual cycle (around on 28 day average)
Secondary Hamstring muscles cross sectional area Differences according to menstrual cycle phase in hamstring muscles cross sectional area, as measured by ultrasound echography. Length of a menstrual cycle (around on 28 day average)
Secondary Hamstring tendons length Differences according to menstrual cycle phase in hamstring tendons length, as measured by ultrasound echography. Length of a menstrual cycle (around on 28 day average)
Secondary Maximal knee joint range of motion Measure of the volunteer maximal knee range of motion, the maximum being defined by the volunteer as the greatest hip/leg angle reachable without feeling pain. The process is slowly conducted on an isokinetic ergometer by extending the knee joint (2°/s) until the volunteer reaches her maximal range of motion, at which point the movement is stopped and a security is placed. Length of a menstrual cycle (around on 28 day average)
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