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Clinical Trials/NCT03131830
NCT03131830CompletedNot Applicable

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

University Hospital Tuebingen1 site in 1 country2,605 target enrollmentStarted: April 1, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
2,605
Locations
1
Primary Endpoint
Delivery mode

Study Overview

Brief Summary

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.

Detailed Description

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.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • able to fill out a questionnaire

Exclusion Criteria

  • minor people

Arms & Interventions

Pregnant women from Tübingen and Heidelberg

Online-based questionnaire

Intervention: Online-based questionnaire (Other)

Staff of the University Clinic of Tuebingen

Online-based questionnaire

Intervention: Online-based questionnaire (Other)

Participants of the 9th German Urogynecological Congress

Online-based questionnaire

Intervention: Online-based questionnaire (Other)

All members of the German Society of Obsetrics and Gynecology

Online-based questionnaire

Intervention: Online-based questionnaire (Other)

Outcomes

Primary Outcomes

Delivery mode

Time Frame: 3 months

Choice of delivery mode

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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