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Information and Accompaniment of Siblings Following the Announcement of a Cancer in Pediatric Hematology.

U

University Hospital, Lille

Status

Terminated

Conditions

Malignant Haemopathy

Treatments

Other: semi-directive interview

Study type

Interventional

Funder types

Other

Identifiers

NCT03541330
2016-A02091-50 (Other Identifier)
2016_83

Details and patient eligibility

About

The primary objective is to evaluate the experience with the information received on the disease by the healthy brothers and sisters of childrens with malignant haemopathy at the Centre Hospitalier Régional et Universitaire of Lille

Enrollment

7 patients

Sex

All

Ages

6 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Children from 6 to 12 years old
  • Brother or sister of a child:

O has malignant haemopathy O follow-up in the pediatric hematology department in Lille, O diagnosed from 6 weeks to 1 year before maintenance of the healthy subject included

  • whose parents are able to understand and sign voluntarily informed consent
  • Affiliated to a social security scheme
  • Ability to understand and answer questions alone during the semi-structured interview

Exclusion criteria

  • Child under 6 years or over 12 years
  • Subject with a pathology that may interfere with the course of the study, according to the investigator's assessment
  • Absence of the informed consent of one of the parents and / or the legal representative
  • Refusal of participation of the subject

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

7 participants in 1 patient group

siblings
Other group
Description:
Brother or sister of a child has malignant haemopathy and follow-up in the pediatric hematology department
Treatment:
Other: semi-directive interview

Trial contacts and locations

1

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Central trial contact

Eva De Berranger, MD

Data sourced from clinicaltrials.gov

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