Requests for Medical Termination of Pregnancy for Psychological or Social Maternal Reasons

August 11, 2022 updated by: Centre Hospitalier de Saint-Denis

Requests for Medical Termination of Pregnancy for Psychological or Social Maternal Reasons at the "Maison Des Femmes" in Saint-Denis : Retrospective Study Between 2016 and 2022

When the request for termination of pregnancy is made at a term of less than sixteen weeks of amenorrhea, the patients have complete decision-making autonomy. This is called voluntary termination of pregnancy. On the other hand, when they are made after this term, their requests must be subject to a multidisciplinary assessment. This is called medical termination of pregnancy for maternal indication. Schematically, there are two categories of indications: "organic" (progressive cancer, severe heart disease, etc.) and "psycho-social". In the latter case, and although the recommendations of the CNGOF recommend a formalization of these requests in the centers where the patients are received, strong disparities are observed in practice. In addition, there are few epidemiological and clinical data concerning these medical terminations of pregnancy with a psychological or social maternal indication in the literature.

The objective of this work is to describe the demographic characteristics of patients who have made a request for termination of pregnancy after the legal deadline for psychological or social maternal reasons, and to specify the care pathways of these patients.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Retrospective cohort (from 01/01/2016 to 02/28/2022) single-centre involving data from patients followed at the Maison des Femmes, and eligible for the study.

The demographic and care pathway variables will be the subject of a descriptive statistical analysis.

Expected results: improvement of knowledge relating to patients who consulted for termination of pregnancy after sixteen weeks of amenorrhea and their care pathway.

Outlook:

  • Improving the knowledge of health professionals and therefore of care pathways, with a view to a more homogeneous use of legal systems.
  • Improvement and simplification of care pathways.

Study Type

Observational

Enrollment (Anticipated)

120

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Patients followed at the Maison des Femmes, having consulted between 01/01/2016 and 02/28/2022, having undergone a medical termination of pregnancy for psychological or social maternal reasons

Description

Inclusion Criteria:

  • Minor or adult patients who have been seen at the Maison des Femmes in the context of a request for termination of pregnancy for psychological and/or social maternal reasons, including patients subject to a legal protection measure (guardianship , curators) during the consultation
  • Consultation between 01/01/2016 and 02/28/2022

Exclusion Criteria:

  • Refusal of inclusion in a study explained in the medical file (patient or guardian)
  • Objection to the use of data or refusal to participate (patient or guardian)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
age
Time Frame: Day 1
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1
place of life
Time Frame: Day 1
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1
social security
Time Frame: Day 1
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1
level of studies
Time Frame: Day 1
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1
occupation / resources
Time Frame: Day 1
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1
marital status
Time Frame: Day 1
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1
number of children
Time Frame: Day 1
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1
native country
Time Frame: Day 1
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1
recent life events
Time Frame: Day 1
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
migratory route
Time Frame: Day 1
care pathway for patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1
medical and surgical history
Time Frame: Day 1
care pathway for patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1
gynecological follow-up, and follow-up of the current pregnancy
Time Frame: Day 1
care pathway for patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
Day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ANTICIPATED)

August 17, 2022

Primary Completion (ANTICIPATED)

August 17, 2022

Study Completion (ANTICIPATED)

November 30, 2022

Study Registration Dates

First Submitted

August 11, 2022

First Submitted That Met QC Criteria

August 11, 2022

First Posted (ACTUAL)

August 12, 2022

Study Record Updates

Last Update Posted (ACTUAL)

August 12, 2022

Last Update Submitted That Met QC Criteria

August 11, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • CHSD_0028_MATER

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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