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NCT Number: NCT06884046

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

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.

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Key information

Age range

0 day–28 day

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

Personalized support project

Other
  • Presence of a child nurse at the consultation of the anesthesiologist-resuscitator.
  • Antenatal paramedical consultation conducted by a child nurse composed of a semi-structured interview and an evaluation of Parental Stress by the ISP-4 self-questionnaire.
  • Implementation of the personalized support project
  • Self-assessment of parental stress using the ISP-4 self-questionnaire (child admitted to intensive care or resuscitation unit)
  • Application of the personalised support project
  • Self-assessment of parental stress using the ISP-4 self-questionnaire (child discharged from intensive care)
  • Paramedical follow-up consultation with parents (semi-directive interview, ISP-4 self-questionnaire) and assessment of the child's psychomotor development in the child's 6th month of life

Primary outcomes

  1. Families participation evaluation

    Time frame: 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.

Secondary outcomes

  1. Parental stress Evolution

    Time frame: between visit 1 (day -28) and visit 6 (day 180)

    Evolution of parental stress by the ISP-4 self-questionnaire (Parental Stress Index)

  2. Infant development

    Time frame: at the last protocol visit ( visit 6 - day 180)

    Evolution of the overall score of the Bayley-4 scale (Bayley Infant and Young Child Development Scales) at 6 months of life compared to a literature cohort (neonate child).

  3. Evaluation of the healthcare team adherence

    Time frame: at visit 5 ( day 60 )

    Evaluation of the adherence of the healthcare team to this new model via a Likert scale administered at the discharge of the child, and an analysis of the large items found on the accompanying sheets

  4. Evaluation of the healthcare team adherence

    Time frame: at visit 5 ( day 60 )

    Evaluation of the adherence of the healthcare team to this new model via an EVA scale administered at the discharge of the child, and an analysis of the large items found on the accompanying sheets

  5. Personal Support Project Evaluation

    Time frame: at the last protocol visit ( visit 6 - day 180)

    Evaluation of the Personal Support Project by families using an Visual Analogue Scale.

Study contacts

Contact information is provided by the study sponsor or research team.

Amandine RUISSEL

CONTACT

[email protected]

+33 05 57 62 32 29 ext. +33

Laurie PONTEINS

CONTACT

[email protected]

+33 05 57 65 67 93 ext. +33

Sponsors and collaborators

Lead sponsor

University Hospital, Bordeaux

Other

Registry information

Official study title

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

Acronym: Et APRéS Ca

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Mar 19, 2025
Registry last updated
Mar 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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