Delivery Mode Clinical Trial
Official title:
Individual Choice of Delivery Mode - A Prospective Study Using Online Surveys
NCT number | NCT03131830 |
Other study ID # | DECISION |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | April 1, 2017 |
Est. completion date | May 1, 2018 |
Verified date | April 2017 |
Source | University Women's Hospital Tübingen |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
Status | Completed |
Enrollment | 2605 |
Est. completion date | May 1, 2018 |
Est. primary completion date | January 1, 2018 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - able to fill out a questionnaire Exclusion Criteria: - minor people |
Country | Name | City | State |
---|---|---|---|
Germany | University Women's Hospital | Tübingen |
Lead Sponsor | Collaborator |
---|---|
University Women's Hospital Tübingen | Deutsches Beckenbodenzentrum, Berlin, Germany, Universitätsfrauenklinik, Heidelberg, Germany, University of Michigan |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Delivery mode | Choice of delivery mode | 3 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
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