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Clinical Trials/NCT03283189
NCT03283189UnknownNot Applicable

Perception of the Risk Associated With the Use of Cosmetics Products During Pregnancy - a Qualitative Study

University Hospital, Clermont-Ferrand1 site in 1 country60 target enrollmentStarted: February 28, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Pregnant women's views on the risk related to the use of cosmetics

Study Overview

Brief Summary

The use of cosmetics is an important source of exposure to many chemicals including endocrine disruptors. Recently, national and international scientific recommendations have been issued to limit exposure to chemicals during pregnancy. However, the perception and the use of cosmetics by pregnant women is still little studied. The objectives of the PERICOS study are to identify the risk perception and the attitudes regarding cosmetic's use by the pregnant women.

Understanding the risk perception, the knowledge, attitudes and expectations of women about the use of cosmetics during pregnancy will help to set up effective strategies to improve prevention of chemical exposure.

Detailed Description

A qualitative study of 60 pregnant women using six focus groups (9-11 pregnant women per group) was implemented study in Auvergne Region, France. Six focus groups will be conducted until data saturation.

The women will be recruited from the Clermont-Ferrand University Hospital (maternity type III - 2 groups), the private clinic in Beaumont (maternity type II - 2 groups), the Saint-Flour hospital center (maternity type I - 1 group), and from liberal health professionals (1 group).

If a women is found to be eligible, she will be invited to participate in the study. The focus group discussions will be conducted in a private room in the maternity of the women. They will last approximately 2 hours and will be led by an interviewer using an interview grid.

All interviews will be audio-recorded, transcribed, coded and computerized for analysis with the NVIVO v11 software.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Cross Sectional

Eligibility Criteria

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

Inclusion Criteria

  • - Pregnant women between 22 (≥ 22 weeks) et ≤ 39 weeks of gestation;
  • Obstetric management in the Réseau de Santé en Périnatalité d'Auvergne (RSPA);
  • At least 18 years;
  • Understanding and speaking French;
  • And giving their signed agreement of participation.

Exclusion Criteria

  • Refusal to participate or to be registered during the collective interview;
  • Women with fetal death in utero or whose fetus or fetuses have a malformation;
  • Women with psychiatric disorders, mental confusion or language disorders making impossible the interview;
  • Women with chronic dermatological pathology requiring dermatological care (eczema, psoriasis, etc.).

Outcomes

Primary Outcomes

Pregnant women's views on the risk related to the use of cosmetics

Time Frame: at day 1 (during the interview)

the perception of the risks linked to the use of cosmetics in general, and creams for striae gravidarum in particular, were investigated during the focus groups interviews.

Secondary Outcomes

  • Cosmetic's use during pregnancy(at day 1 (during the interview))
  • Expectations of pregnant women in terms of information about the use of cosmetics(at day 1 (during the interview))

Investigators

Sponsor
University Hospital, Clermont-Ferrand
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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