跳至主要内容
临床试验/NCT02834130
NCT02834130已完成不适用

Input of a Multidisciplinary Device Including a Psychological Approach, to Accompany the Announce of Diagnosis for Young Children With Serious Constitutional Hemorrhagic Disease and Their Families

Assistance Publique Hopitaux De Marseille2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2014年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
2
主要终点
Number of Treatment Exposure Days compared to the Number of Treatment Exposure days prescribed

研究概览

简要总结

Severe forms of hemophilia and other constitutional bleeding disorders represent a group of rare diseases. In last decades, news therapies have dramatically increased life expectancy and joint's protection.

The investigators propose to set up a single-centre, descriptive, transversal pilot study, designed for the inclusion of around thirty children from 2 to 10 years, with haemophilia or allied hereditary bleeding disorders (HBD), who were referred to the Hemophilia Treatment Center (HTC) of Marseille at diagnosis. For those children who were able to benefit from the totality or part of the device accompanying the diagnostic announcement in the past 10 years.

详细描述

Severe forms of hemophilia and other constitutional bleeding disorders represent a group of rare diseases. In last decades, news therapies have dramatically increased life expectancy and joint's protection. The recurrence of joint bleedings is responsive of multifocal arthropathy in the natural history, but nowadays, the orthopedic outcome is good thanks to prophylactic treatments.

However, the announcement of the diagnosis of such hereditary bleeding disorders at a very young age represents a real psychological trauma for parents. Such an announcement may induce some psycho-developmental impairment.

An innovative support has been implemented at the Hemophilia Treatment Center in Marseille, in conjunction with the French Hemophilia Society. This program is based on a multidisciplinary partnership that favors the psychological support and the reinsurance of the parents.

With Rare Diseases Foundation support, the investigators have initiated this pilot study that will include more than 20 patients with severe hemophilia or constitutional bleeding disorder, who benefit from the device. This descriptive, monocentric, interventional study will permit to describe the psychological status, the quality of life of patients and their parents, but also to evaluate the impact of the device on initiation and observance of treatments like Long Term Prophylaxis.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
3 Years 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Patients aged between 3 and 12 years
  • Patients diagnosed and treated at the Center until inclusion
  • Patients with FVIII :C < 2% or with FIX :C <2% or with FVII:C <2% or with FXIII:C <2% or fibrinogen <0,2 g/l, or with type 3 von Willebrand diseases or Thrombasthenia of Glanzmann diseases.
  • Patient who participate to multidisciplinary support and announcement of diagnosis device
  • Voluntarily given fully informed written and signed consents obtained before any study-related procedures are conducted

排除标准

  • Patient with other clotting disorder or disease.
  • Patient diagnosed or treated in other centre
  • Patient with psychiatric disorder or disease
  • Patient with other severe chronic disease

结局指标

主要结局

Number of Treatment Exposure Days compared to the Number of Treatment Exposure days prescribed

时间窗: 2 years

Treatment Observance

次要结局

  • Assessment of patient's behavioral condition using the Child Behavior Check-list (CBCL) 1,5-5(2 Years)
  • Assessment of the patient's body consciousness through the "CORP-R" test (french test of body mapping)(2 years)
  • Assessment of patient's quality of life using the "Kidscreen" questionnaire for children(2 years)
  • Assessment of the patient's parents' Qaulity of life through the Short Form Health Survey (SF-36)(2 Years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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