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AzTrials

DeliveryIDEANCT06803979

Impact of Delivery Method Elite Athletes.

An observational study of Delivery and Performance, run by Faculty Hospital Kralovske Vinohrady at 1 site in Czechia.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Labor itself can occur spontaneously vaginally, with the help of extraction methods, or via cesarean section. It can also be planned or awaited for the spontaneous onset of uterine contractions. Read more about this study

Who is it for?
Any age, women onlyHealthy volunteers can take part
Conditions the study is for
Delivery, Performance, Caesarean Section
How many people
500 participants
Where
1 siteCzechia
Study dates
16 Mar 2025to 1 Jan 2040
How long will I take part?
100 Years
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • Women only
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: General young population for compering with the group of elite athletes which are meeting representation limits and included in national teams organized under the Czech Olympic Committee and individual sports federations.

Who may be able to join

  • Elite female athletes meeting representation limits and included in national teams organized under the Czech Olympic Committee and individual sports federations.

Who cannot join

  • Any male

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Jan Zapletal, MUDr. contact

+420607882602

honza.zaple@seznam.cz

Czechia1 site, 1 recruiting
  • Faculty Hospital Kralovske Vinohrady

    Prague, 11000

    Jan Zapletal, MD, +420607882602, honza.zaple@seznam.cz

    Recruiting

Other trials in Czechia

About this study

Official title: The Impact of Delivery Method on the Performance of Elite Athletes.

Labor itself can occur spontaneously vaginally, with the help of extraction methods, or via cesarean section. It can also be planned or awaited for the spontaneous onset of uterine contractions. Each method has its advantages and disadvantages regarding potential damage to the pelvic floor and its stability in vaginal delivery or extraction methods, or concerning the stability of the abdominal wall with subsequent wound healing after a cesarean section.

The aim of the study is to retrospectively and prospectively determine the impact of the method of delivery on the performance of female athletes through a questionnaire study. Investigators would like to answer the question of whether cesarean delivery means a later return to training for athletes, whether pregnancy is problematic for female athletes in relation to their BMI, and whether pregnancy often signifies the end of a sports career for female athletes. The questionnaire also includes questions regarding overall women's health-menstrual cycle, incontinence, and mental health of female athletes. Prospectively, the questionnaire will be sent to all female athletes who meet representation limits once a year and for two years after retiring from the national team.

Read the detailed description

Childbirth and pregnancy are among the most significant moments in a woman's life. The method of delivery is currently a highly debated topic with potential impacts on a woman's future physical and mental health. For elite female athletes, this issue is amplified, as pregnancy and childbirth significantly affect their performance and careers, and it is often necessary to plan pregnancies in consideration of current sporting events and ongoing physical training.

Labor itself can occur spontaneously vaginally, with the help of extraction methods, or via cesarean section. It can also be planned or awaited for the spontaneous onset of uterine contractions. Each method has its advantages and disadvantages regarding potential damage to the pelvic floor and its stability in vaginal delivery or extraction methods, or concerning the stability of the abdominal wall with subsequent wound healing after a cesarean section.

The aim of the study is to retrospectively and prospectively determine the impact of the method of delivery on the performance of female athletes through a questionnaire study. The investigators would like to answer the question of whether cesarean delivery means a later return to training for athletes, whether pregnancy is problematic for female athletes in relation to their BMI, and whether pregnancy often signifies the end of a sports career for female athletes. The questionnaire also includes questions regarding overall women's health-menstrual cycle, incontinence, and mental health of female athletes. Prospectively, the questionnaire will be sent to all female athletes who meet representation limits once a year and for two years after retiring from the national team.

Keywords
delivery, performance, caesarean section, pregnancy, athletes, women health

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06803979
Study groupRoleWhat they receive
Retires elite athletesElite athletes with finished sport career
Elite athletes currently performing sportCurrent elite athletes who are still doing sports and who will be asked about their career changes prospectively every year
General populationGeneral population for comparing with previous groups

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Performance

    Best score will be used to compare performance of the athletes prior to delivery and after delivery

    Measured: 2 years retrospectively and through study completion, an average of 5 years

  2. Performance

    Best time will be used to compare performance of the athletes prior to delivery and after delivery

    Measured: 2 years retrospectively and through study completion, an average of 5 years

  3. Performance

    Most points scored will be used to compare performance of the athletes prior to delivery and after delivery

    Measured: 2 years retrospectively and through study completion, an average of 5 years

  4. Placement of athletes during competitions

    Best achievements according to athletes (for example 3rd place on Olympic Games) prior to delivery and after delivery

    Measured: Prior to delivery and 2 years after the delivery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 Jan 2025
  2. Study start16 Mar 2025 (estimated)
  3. Primary completion1 Jan 2040 (estimated)
  4. Study completion1 Jan 2040 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Other
Enrolment
500 participants (estimated)
Target duration
100 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT06803979
Sponsor's protocol ID
EK-VP/53/2024
Acronym
IDEA
Status last verified
Mar 2025
First submitted
20 Jan 2025
Last updated
18 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Study protocol, Ethical approval, Informed consent

Questions about this trial

What is this clinical trial studying?

An observational study of Delivery and Performance, run by Faculty Hospital Kralovske Vinohrady at 1 site in Czechia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 18 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Czechia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Jan Zapletal, MUDr. (+420607882602, honza.zaple@seznam.cz), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Performance (time frame: 2 years retrospectively and through study completion, an average of 5 years). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Mar 2025.

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