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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03651843
Other study ID # 2017_88
Secondary ID 2018-A00962-53
Status Completed
Phase
First received
Last updated
Start date September 4, 2018
Est. completion date November 30, 2018

Study information

Verified date October 2019
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In ten years, the labor force has grown by 1.4 million people according to French national institute for statistical and economic studies. This increase is partly due to the increased presence of women in the labor market. Thus, the majority of some 800,000 annual births come from working women. However, some women in professional activity may be exposed to occupational risks, which may have effects on the develop-ment of the fetus during pregnancy. France benefits from protective legislative measures against pregnant women. Recommendations already exist.

But with medical desertification, pregnant women may have more difficulty contacting their occupational doctor or treating physician and to access information about the risks to her work-related pregnancy.

It seems to us important to be able to better quantify the information needs of women in this problem.


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date November 30, 2018
Est. primary completion date November 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- working during their pregnancy (at least 2 months, including the beginning of pregnancy

- having given birth during the period of inclusion

- in a hospital or clinic of Lille metropolis volunteer to participate in the study

Exclusion Criteria:

- minor women

- unemployed

- student

- guardianship

- work abroad

- change of employer during pregnancy

- inability to answer the questionnaire

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Questionnaire
Women who have recently given birth in the Lille metropolitan area fill in a self-administered questionnaire asking them about their perception of occupational risk during pregnancy and their knowledge of their right to work during pregnancy.

Locations

Country Name City State
France Hôpital Claude Huriez, CHU Lille

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary percentage of women who thought they had occupational exposures at risk for their baby during pregnancy the different occupational exposures are listed. If the woman has been exposed and thinks it's dangerous for her baby, she reports it. At childbirth
Secondary adaptation or not of the workstation in case of exposure to a professional risk if the woman is exposed to a defined risk and her job has been set up to avoid this risk during pregnancy, she reports it at childbirth
Secondary percentage of women with a score of at least 5 out of 10 knowledge of French legislation concerning the protection of pregnant women at work of current legislation referenced in a questionnaire that includes 10 binary questions. A score will be calculated by summing the answers (score out of 10) at childbirth
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