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OpenTrials
Completed

NCT Number: NCT03131830

Individual Choice of Delivery Mode

The primary aim of the study is to investigate personal attitudes regarding mode of delivery among both medical health care professionals and non-professionals. The investigators are also investigating whether providing detailed information that might influence one's decision regarding mode of delivery (such as education on pelvic floor disorders or advantages or disadvantages of epidural anaesthesia) will change participants´ opinion how to determine their preferred mode of delivery.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Women's Hospital

Tübingen, 72076, Germany

About this study

The choice of delivery mode is an individual decision that is affected by personal opinions and feelings about what might be best for one's own body and child. Increasing awareness about the risks of vaginal delivery has led to an increasing rate of cesearean delivery on maternal request.

The primary aim of the study is to investigate personal attitudes regarding mode of delivery among both medical health care professionals and non-professionals. The investigators are also investigating whether providing detailed information that might influence one's decision regarding mode of delivery (such as education on pelvic floor disorders or advantages or disadvantages of epidural anaesthesia) will change participants´ opinion how to determine their preferred mode of delivery.

A secondary aim of the survey is to gather information about personal attitudes regarding:

  • epidural anaesthesia for pain relief during delivery
  • systems of risk stratification
  • postnatal recovery exercises The data will be acquired with an online questionnaire designed for this study. There will be two groups in this study. The first group ("medical professionals") consists of gynecologists with either subspecialization (urogynecology , fetal and maternal medicine, obstetrics, other) and other non-OB/GYN health care providers and medical staff, regardless whether they are nurses, medical assistants, physicians, physiotherapists, midwifes, administration staff. The group of "non-professionals" consists of women who are currently pregnant, and are not healthcare professionals.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • able to fill out a questionnaire

Exclusion criteria

  • minor people

Treatment and study plan

Online-based questionnaire

Other

Participants receive a web-link to a questionnaire, which is active for 3 months

Primary outcomes

  1. Delivery mode

    Time frame: 3 months

    Choice of delivery mode

Sponsors and collaborators

Lead sponsor

University Hospital Tuebingen

Other

Registry information

Official study title

Individual Choice of Delivery Mode - A Prospective Study Using Online Surveys

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Apr 27, 2017
Registry last updated
Feb 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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