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Access to Maternity and Risk Factors in a Non-consultant Population (PROXIMA)

Access to Maternity and Risk Factors in a Non-consultant Population - Longitudinal and Prospective Exploratory Study (PROXIMA)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04506489
Enrollment
500
Registered
2020-08-10
Start date
2019-07-01
Completion date
2021-01-01
Last updated
2020-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Partum Depression

Brief summary

Characterize the psychic and medical disorders related to pregnancy and motherhood in a group of primiparous and primigratic women.

Interventions

OTHERPsychological investigation

Psychological tests, psychological interviews.

Sponsors

Centre Hospitalier Universitaire de Besancon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* primiparous and primigest women, * Singleton pregnancy * Consultant at the University Hospital of Besançon in gynecology / obstetrics department - initial consultation * 25 to 45 years old, * European culture and speaking French, * Living in a relationship with the spouse * Spontaneous pregnancy, without medical help * Having agreed to the use of this medical data as part of this research and the completion of the self-questionnaires. * Patients who benefit from a social security scheme

Exclusion criteria

* Termination of pregnancy or non-progressive pregnancy * Prematurity of the child (Childbirth before 37 weeks) * Maternal pathologies acquired during pregnancy * Fetal diseases acquired during pregnancy * Pregnancy of twins or triplets * Any type of medical difficulties occurring during pregnancy (gestational diabetes, high blood pressure, threat of preterm delivery, preeclampsia, ...) * Any type of difficulty occurring during childbirth for example, hemorrhage of maternal deliverance * Birth by cesarean section Birth necessitating the use of instruments that led to the transfer of the baby to the neonatology unit or to the kangaroo unit * At birth, baby's Apgar less than 7. * Fetal death * Childbirth that did not occur at the CHU maternity ward

Design outcomes

Primary

MeasureTime frameDescription
Self questionnaire : health, Anxiety, Postnatal, Body Satisfaction, , Bartholomew, RelationShip, Social , Perinatal, Family Relationship , parental stress, dyadic alliance, Parental Bonding , Prenatal attachment , birth experience3 to 4 months of pregnancyunits (scale)

Countries

France

Contacts

Primary ContactBelot Rose Angélique, MCF
rose-angelique.belot@univ-fcomte.fr0680188113
Backup ContactPointurier Mathilde
mathilde.pointurier@edu.univ-fcomte.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026