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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04420169
Other study ID # B670201627388
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2016
Est. completion date December 2021

Study information

Verified date February 2023
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Dutch-speaking women who are about to start an IVF treatment will be approached. If they are willing to participate in the study, they will receive an email with a link to an online questionnaire. This questionnaire will evaluate the communication by the midwive in preparation for an IVF treatment. When 50 women have completed the questionnaire a standardized communication protocol will be enrolled. Once all midwives are trained, 50 other IVF patients will be asked to complete the slightly adapted post questionnaire.The data from both questionnaires will be compared.


Recruitment information / eligibility

Status Completed
Enrollment 105
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - women who are about to start an IVF treatment at our department Exclusion Criteria: - non-Dutch speaking - women who are counseled by one of the midwives involved in the design of this study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Questionnaire
A digital questionnaire to evaluate the communication by midwives will be send out to IVF patients

Locations

Country Name City State
Belgium Ghent University Hospital Gent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary How do patients evaluate the communication by the midwife in anticipation of the IVF treatment cycle? Self created questionnaire (no scale) About 20 weeks counting from the launch of each questionnaire or earlier if the target of 50 patients is reached sooner
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