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临床试验/NCT06884046
NCT06884046招募中不适用

Evaluation of the Feasibility of Support for the Management of Parental Stress in Surgical Resuscitation of Congenital Heart Diseases

University Hospital, Bordeaux1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年2月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
40
试验地点
1
主要终点
Families participation evaluation

研究概览

简要总结

Half of children with congenital heart disease develop specific neurodevelopmental disorders. Neurodevelopmental disorders are the leading cause of morbidity in these children. They can be increased by perioperative complications, the family and economic socio-economic environment and the level of parental stress. The stress perceived by parents of children with congenital heart disease varies depending on the time of diagnosis, the organization of care inherent in neonatal management and the type of pathology diagnosed.

The main objective is to evaluate the feasibility of a multidisciplinary and personalised model of support for parental stress, from the ante-natal period, in the context of their child's neonatal cardiac surgery.

详细描述

Congenital heart disease (CC) is the most common congenital malformation. Every year, 8 newborns out of 1000 are affected by these pathologies worldwide and about 20% of them will require intervention in the first days of life. The complexity of heart disease, factors intrinsic to the patient as well as surgical techniques can be the cause of neurological abnormalities. Indeed, 43% of these CC newborns are already carriers of a cerebral anomaly in the perinatal period.

Neurodevelopmental disorders (NDD) are the leading cause of morbidity in these children. They can be increased by perioperative complications, the family and economic socio-economic environment and the level of parental stress. The stress perceived by parents of children with CC varies depending on the time of diagnosis, the type of pathology and the organization of neonatal care.

It is essential to accompany these parents with personalized care. It must be comprehensive, multidisciplinary and empathetic, with the aim of improving the neurodevelopmental prognosis of these children, and family well-being.

Through this project of accompaniment proposed from the antenatal, we innovate by integrating consultations by the paramedical team of the resuscitation, the implementation of a personalized support project that meets the expectations and needs of families for better care of their child. A parental stress assessment will be carried out at 4 times of the family care journey.

研究设计

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

入排标准

年龄范围
0 Days 至 28 Days(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Parents whose fetus has congenital heart disease diagnosed in antenatal, which will be operated in the neonatal period (between 0 and 28 days of life) within our sector.
  • •Parents followed in the congenital heart disease sector of the University Hospital of Bordeaux as soon as the diagnosis is announced in antenatal.
  • •Free, informed and signed written consent of the couple or single mother in a single parent setting or by a third person (in case of physical disability of the participant) and the investigator (no later than the day of inclusion and before any examination required by the research).
  • •Person affiliated or beneficiary of a social security scheme (excluding AME).
  • •Parents with parental authority.

排除标准

  • •Parents who do not understand or read French and cannot be accompanied by a third party for translation.
  • •Parents with major psychiatric disorders.
  • •Parents deprived of liberty due to ongoing legal proceedings.
  • •Parents under guardianship or curatorship or unable to personally express consent.

研究组 & 干预措施

Accompaniment project

Experimental

The experimental intervention envisaged combines specific monitoring and the implementation of a personalised support programme.

干预措施: Personalized support project (Other)

结局指标

主要结局

Families participation evaluation

时间窗: at the last protocol visit ( visit 6 - day 180)

The participation of families in the proposed accompaniment will be evaluated by the participation rate: number of parents who participated in the study until the last stage of the protocol, number of parents who dropped out of the study and reason.

次要结局

  • Infant development(at the last protocol visit ( visit 6 - day 180))
  • Evaluation of the healthcare team adherence(at visit 5 ( day 60 ))
  • Parental stress Evolution(between visit 1 (day -28) and visit 6 (day 180))
  • Personal Support Project Evaluation(at the last protocol visit ( visit 6 - day 180))

研究者

发起方
University Hospital, Bordeaux
申办方类型
Other
责任方
Sponsor

研究点 (1)

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