This trial is active, not recruiting.

Conditions pregnancy, rural parturient women, precarious situation, epices scale, general practice
Treatment epices scale
Sponsor University Hospital, Clermont-Ferrand
Collaborator Hospital Center of Issoire : Maternity unit
Start date September 2014
End date October 2015
Trial size 190 participants
Trial identifier NCT02275442, CHU-0212


The link between precarious situations and health conditions are more described in previous study. Precarious situations are more frequent and complex especially in rural areas. There are recognized like a risk factor of complications during pregnancy and delivery. It's necessary to describe antenatal cares for rural women in precarious situations to prevent those situations, to understand their difficulties in order to reduce inequalities and health spending.

The aim of the PRUGNANCY study is to understand the difficulties of rural parturient women and the strategies developed to overcome them. Recognized earlier precarious situations and valorized General Practitioners and restore them to the follow-up or parturient women.

United States No locations recruiting
Other countries No locations recruiting

Primary Outcomes

rate for prenatal cares
time frame: at 9 months

Secondary Outcomes

antenatal and postnatal cares
time frame: at day 1
strategies to overcome difficulties to realize antenatal and postanatal cares
time frame: at 2 months

Eligibility Criteria

Female participants of any age.

Inclusion Criteria: - Women old enough to procreate. Precariousness: EPICES scale > 30, 17. Live in rural areas (INSEE definition). Exclusion Criteria: - To be unable to answer the questionnaire: intellectual disability or no French speaker or illiterates. EPICES scale not completed. Women who gave birth to a stillborn child. Medical interruption of pregnancy.

Additional Information

Principal investigator Philippe VORILHON
Description It's a multicenter prospective observational study with a quali-quantitative method. This study involved three maternities in Auvergne region (Issoire, Thiers, Saint-Flour). Precarious women living in rural areas are included. They will be followed during a period of two months after childbirth. The main assessment criterion is the adequation rate between antenatal care for those women and the HAS recommendation's. The amount necessary to highlight a significant difference is 190 patients (IC 95% [0.429 - 0.571] ; risk = 5 % ; Adequation rate = 50 % ; lost to follow-up rate = 10 % ; deprivation rate = 27 %). The secondary criteria of judgment are the reasons for not realized antenatal and postnatal cares, the difficulties of realized antenatal and postnatal cares, the strategies developed to overcome them, the term and health status of the child birth (Apgar score, birth weight), the health status of the child birth and his mother during the two post-partum months (HAS recommendation's).
Trial information was received from ClinicalTrials.gov and was last updated in October 2014.
Information provided to ClinicalTrials.gov by University Hospital, Clermont-Ferrand.