Individual Choice of Delivery Mode
1 other identifier
observational
2,605
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2017
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2017
CompletedFirst Submitted
Initial submission to the registry
April 24, 2017
CompletedFirst Posted
Study publicly available on registry
April 27, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2018
CompletedFebruary 12, 2026
April 1, 2017
9 months
April 24, 2017
February 9, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Delivery mode
Choice of delivery mode
3 months
Study Arms (4)
Staff of the University Clinic of Tuebingen
Online-based questionnaire
Participants of the 9th German Urogynecological Congress
Online-based questionnaire
All members of the German Society of Obsetrics and Gynecology
Online-based questionnaire
Pregnant women from Tübingen and Heidelberg
Online-based questionnaire
Interventions
Participants receive a web-link to a questionnaire, which is active for 3 months
Eligibility Criteria
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. Inclusion Criteria: Participants in the "medical professionals" group can be from either gender, over age 18, currently working in the medical profession and have sufficient understanding of the German language in order to be able to fill out the questionnaire. The "non-professionals" are pregnant females over age 18 with sufficient understanding of the German language in order to be able to fill out the questionnaire.
You may qualify if:
- able to fill out a questionnaire
You may not qualify if:
- minor people
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Women's Hospital
Tübingen, 72076, Germany
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 24, 2017
First Posted
April 27, 2017
Study Start
April 1, 2017
Primary Completion
January 1, 2018
Study Completion
May 1, 2018
Last Updated
February 12, 2026
Record last verified: 2017-04
Data Sharing
- IPD Sharing
- Will not share