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First Trimester of Pregnancy: Impact of a History of Miscarriage on Women's Stress

NCT ID: NCT04841486

Last Updated: 2021-12-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

93 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-06-11

Study Completion Date

2021-11-05

Brief Summary

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Miscarriage is the spontaneous termination of pregnancy before 22 weeks of amenorrhea. The most frequent complication of pregnancy, it represents 10 to 25% of pregnancies and affects one in four women.

Miscarriage is considered by medical personnel to be common and trivial. however, for women, it is very often a traumatic event, a source of worry for futures pregnancies.

Detailed Description

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The aim of the study is to evaluate association between history of spontaneous termination of pregnancy and women's stress during the first trimester of pregnancy.

Conditions

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Pregnancy

Keywords

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pregnancy women's stress history of spontaneous termination of pregnancy

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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"with history of spontaneous termination of pregnancy" group

pregnant women in the first trimester of pregnancy with history of spontaneous termination of pregnancy

Data collection

Intervention Type OTHER

evaluation of women's stress

"without history of spontaneous termination of pregnancy" group

pregnant women in the first trimester of pregnancy without history of spontaneous termination of pregnancy

Data collection

Intervention Type OTHER

evaluation of women's stress

Interventions

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Data collection

evaluation of women's stress

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* female
* pregnant (positive plasma HCG)
* in the first trimester of pregnancy
* aged 18 years old and more
* agreeing to participate in the study

Exclusion Criteria

\- less than 18 years old
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Université de Reims Champagne-Ardenne

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sandra CARRAU-TRUILLET, MD

Role: PRINCIPAL_INVESTIGATOR

Université de Reims Champagne-Ardenne - CHU de Reims

Locations

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Université de Reims Champagne-Ardenne

Reims, , France

Site Status

Countries

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France

Other Identifiers

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2021-001-Stress-FC

Identifier Type: -

Identifier Source: org_study_id