Study Results
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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COMPLETED
9 participants
OBSERVATIONAL
2019-01-14
2019-04-11
Brief Summary
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The aim of the study is to describe parents' experience for a better understanding and a better care.
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Interventions
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Semi-structured interviews
The purpose of this study is to describe the experience of pregnancy by parents who have chosen to carry to term despite a lethal fetal diagnosis. Therefore, semi-structured interviews will be conducted to explore the links between context, feeling, involvement, decision and actions during pregnancy, whether within the couple or in its environment.
Eligibility Criteria
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Inclusion Criteria
* Participants must have received the information and not have objected to participating in the study,
* the lethal / adverse short-term prognosis of the fetal pathology must have been confirmed by a committee of experts (CPDPN),
* The choice to continue the pregnancy should have been clearly expressed,
* The birth of the child should not be older than 24 months.
* The child's death must be more than 6 months old (or not have occurred)
Exclusion Criteria
* Measure of legal protection of one of the members of the couple (guardianship, trusteeship, ...),
* Severe psychiatric or neurological disorders inducing significant cognitive impairment.
18 Years
ALL
Yes
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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Équipe de psychopathologie périnatale - Service de psychopathologie du développement - Centre Hospitalier Femme-Mère-Enfant - Hospices Civils de Lyon
Bron, , France
Service de gynécologie obstétrique - Hôpital de la Croix Rousse
Lyon, , France
Service de gynécologie-obstétrique - Centre hospitalier Lyon sud
Pierre-Bénite, , France
Countries
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Other Identifiers
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69HCL18_0371
Identifier Type: -
Identifier Source: org_study_id
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