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PS IVG : Psychosocial Determinants of Late-term Abortions (14-16 Weeks' Gestation) at Avignon Hospital

PS IVG : Psychosocial Determinants of Late-term Abortions (14-16 Weeks' Gestation) at Avignon Hospital

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07650071
Acronym
PS IVG
Enrollment
30
Registered
2026-06-16
Start date
2026-06-15
Completion date
2027-09-15
Last updated
2026-06-16

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

Conditions

Abortion, Psychosocial Health

Brief summary

Abortion is a fundamental right for women in France, where the legal time limit was extended from 14 to 16 weeks' gestation. This extension allows women, whose psychosocial determinants are poorly known, and who face various obstacles (personal, administrative, medical, or other), to access abortion. However, it may also expose them to psychological troubles and difficulties in accessing healthcare. This study aims to identify the psychosocial determinants and disruptions in the primary care pathway associated with late abortions (≥14 weeks' gestation \[WG\]) in order to propose preventive actions, particularly regarding contraception, screening, and referral, directly applicable in general practice.

Interventions

BEHAVIORALHealth survey

It consists of a single anonymous questionnaire, to be completed once only, on a secure online platform, accessed using a QR code provided directly by the healthcare professional. The questionnaire consists of 39 main questions, predominantly with closed-ended response options. The average completion time is estimated between 10 and 20 minutes.

Sponsors

Centre Hospitalier Henri Duffaut - Avignon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient aged ≥ 18 years * Pregnancy ≥ 14 weeks' gestation * Patient attending Avignon Hospital for a surgical abortion * Willing to participate in the study

Exclusion criteria

* Medical abortion (non-surgical means of abortion) * Ectopic pregnancy * Inability to complete the questionnaire * Patients under legal protection measures (guardianship, curatorship, or court-ordered protection)

Design outcomes

Primary

MeasureTime frame
Describe the sociodemographic profile of patients undergoing late-term abortion at Avignon Hospital.Inclusion

Secondary

MeasureTime frame
Proportion of patients who attended the hospital for a late-term abortion following a general practitioner's recommendation.Inclusion
Proportion of patients who involved their general practitioner in the care pathway for late-term abortions.Inclusion
Descriptive analysis of patients' medical follow-up, medical history and contraceptive practices.Inclusion
Frequency of reasons leading to pregnancy and circumstances of pregnancy discovery.Inclusion
Descriptive analysis of patients' relationships with their entourage regarding this pregnancy (partner, family, healthcare professionals, etc.).Inclusion
Frequency of reasons for choosing abortion.Inclusion
Frequency of late-term abortions performed with the support of a general practitioner.Inclusion
Frequency of late abortions performed under coercion.Inclusion
Frequency of late abortions related to issues in the care pathway.Inclusion
Descriptive analysis of patients' difficulties in accessing this type of healthcare.Inclusion

Countries

France

Contacts

CONTACTMarilyne Grinand, PhD
grinand.marilyne@ch-avignon.fr(+33)432759392
PRINCIPAL_INVESTIGATORPerrine Mazet, MD

Centre Hospitalier d'Avignon, Service de Gynécologie

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 17, 2026