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

NCT ID: NCT03541330

Last Updated: 2025-12-11

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

TERMINATED

Clinical Phase

NA

Total Enrollment

7 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-10-22

Study Completion Date

2019-04-01

Brief Summary

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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

Detailed Description

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Conditions

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Malignant Haemopathy

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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siblings

Brother or sister of a child has malignant haemopathy and follow-up in the pediatric hematology department

Group Type OTHER

semi-directive interview

Intervention Type OTHER

semi-structured interview conducted by a clinical psychologist

Interventions

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semi-directive interview

semi-structured interview conducted by a clinical psychologist

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

6 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Lille

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Eva De Berranger, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Lille

Locations

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Hôpital Jeanne de Flandres, CHU

Lille, , France

Site Status

Countries

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France

Other Identifiers

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2016-A02091-50

Identifier Type: OTHER

Identifier Source: secondary_id

2016_83

Identifier Type: -

Identifier Source: org_study_id

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