Actively Recruiting
Experiences Reported by Siblings of Children Hospitalized in the PICU
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-12-01
20
Participants Needed
2
Research Sites
152 weeks
Total Duration
On this page
Sponsors
A
Assistance Publique - Hôpitaux de Paris
Lead Sponsor
U
URC-CIC Paris Descartes Necker Cochin
Collaborating Sponsor
AI-Summary
What this Trial Is About
The care for a child in pediatric intensive care is recognized as a traumatic experience for the patient and their entourage. The needs and feelings of parents are relatively well supported in the literature. However, there is still too little data concerning siblings, who can nevertheless be impacted by this difficult life experience. The study consists of conducting two semi-structured interviews with siblings of children hospitalized in pediatric intensive care at Necker-Enfants Malades Hospital and Robert Debré Hospital. The first interview will take place during the stay in intensive care, the second one 1 month after discharge from pediatric intensive care.
CONDITIONS
Official Title
Experiences Reported by Siblings of Children Hospitalized in the PICU
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children and adolescents aged 9 to 18 years
- Siblings of a child hospitalized in pediatric intensive care at Necker-Enfants Malades Hospital or Robert Debré Hospital
- Parental authority holders and children/adolescents informed and consenting to participate in the study
You will not qualify if you...
- Death of the patient
- Language barrier if French is not mastered
- Inability to participate in a semi-structured interview due to intellectual disability
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Hôpital Necker-Enfants Malades
Paris, France, 75015
Actively Recruiting
2
Hôpital Robert Debré
Paris, France, 75019
Actively Recruiting
Research Team
L
Léo Dr Berger, Doctor
CONTACT
H
Hélène Morel
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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