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Recruiting NCT06664333

NCT06664333 Experiences Reported by Siblings of Children Hospitalized in the PICU

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Clinical Trial Summary
NCT ID NCT06664333
Status Recruiting
Phase
Sponsor Assistance Publique - Hôpitaux de Paris
Condition Intensive Care Pediatric
Study Type OBSERVATIONAL
Enrollment 20 participants
Start Date 2025-01-21
Primary Completion 2027-12-21

Eligibility & Interventions

Sex All sexes
Min Age 9 Years
Max Age 18 Years
Study Type OBSERVATIONAL
Interventions
Semi-structured interviews

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 20 participants in total. It began in 2025-01-21 with a primary completion date of 2027-12-21.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * Children and adolescents aged 9 to 18 years * Whose sister or brother is hospitalized in pediatric intensive care at Necker-Enfants Malades hospital or Robert Debré hospital * Holders of parental authority and children or adolescents informed and consenting to participate in the study Exclusion Criteria: * Death of patients * Language barrier (French not mastered) * Inability to participate in a semi-structured interview (intellectual disability)

Contact & Investigator

Central Contact

Léo Dr Berger, Doctor

✉ leo.berger@aphp.fr

📞 33671287526

Principal Investigator

Léo MD Berger, Doctor

PRINCIPAL INVESTIGATOR

Assistance Publique - Hôpitaux de Paris

Frequently Asked Questions

Who can join the NCT06664333 clinical trial?

This trial is open to participants of all sexes, aged 9 Years or older, up to 18 Years, studying Intensive Care Pediatric. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06664333 currently recruiting?

Yes, NCT06664333 is actively recruiting participants. Contact the research team at leo.berger@aphp.fr for enrollment information.

Where is the NCT06664333 trial being conducted?

This trial is being conducted at Paris, France, Paris, France.

Who is sponsoring the NCT06664333 clinical trial?

NCT06664333 is sponsored by Assistance Publique - Hôpitaux de Paris. The principal investigator is Léo MD Berger, Doctor at Assistance Publique - Hôpitaux de Paris. The trial plans to enroll 20 participants.

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