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Набор скоро начнётся NCT07692958

Executive Function Intervention for Children With Complex Congenital Heart Disease

Без фазы С лечением Heart Defect, Congenital Executive Dysfunction

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: E-Fit Intervention.
Кому может быть актуально
Состояния в реестре: Heart Defect, Congenital, Executive Dysfunction. Базовые параметры: 9 лет — 13 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Швейцария
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Executive Function Intervention for Children With Complex Congenital Heart Disease: A Randomised Control Study

Обзор

Children with complex congenital heart disease (cCHD) nowadays survive thanks to medical advances into their teenage years and adulthood. However, many of them have difficulties with so-called executive functions. These include skills such as paying attention, planning, self-control, and flexible thinking, which are very important for school, daily life, and becoming independent. These difficulties are linked to changes in the brain and to a higher level of stress. Previous computer-based training programs on their own have either not been very effective, or the effects were lost soon after. In this study, the researchers are testing a newly developed, personalized training program called E-Fit. It combines digital cognitive training, individualized online strategy coaching and analog games. The goal is to find out whether this program can improve executive functions in everyday life for 9-to 13-year-old children with complex congenital heart disease. The study is planed as a randomized controlled trial at the University Children's Hospital Zurich. Children will be assigned either to the training group or to a control group. In addition, the results will be compared with those of a group of healthy children of the same age. The children will visit the University Children's Hospital Zurich three times throughout the whole duration of the study. The first visit will take place before the children start the intervention, the second visit right after the children finished the intervention and the last visit will be 3 months after finishing the intervention. During all these visits neuropsychological assessments, questionnaires, brains scans (MRI) and stress measurements will be collected. The results are intended to help develop effective support programs for these children, improve their well-being, and better prepare them for transition into adulthood.

Вмешательства

  • Другое E-Fit Intervention
    The E-Fit Intervention lasts a total of 12 weeks and consists of three parts: strategy coaching, computerized training, and a analog games. For the strategy coaching, the children meet once a week with a member of the study team. During these sessions, they discuss challenges from their everyday lives and work together to find solutions and develop helpful strategies. In the computerized training, the children train three times per week for 20 minutes each time. The games are designed to impro

Первичные конечные точки

  • Changes in executive functions in everyday life from pre-intervention to post-intervention [Срок оценки: Screening, 3 months]
Вторичные конечные точки (12)
  • Persisting effects of the E-Fit intervention on executive functions in everyday life, 3 months after the post-intervention visit. [Срок оценки: Screening, 3 months, 6 months]
  • Resting-state functional connectivity [Срок оценки: Baseline, 3 months, 6 months]
  • Task-based fMRI activation during executive function tasks [Срок оценки: Baseline]
  • Training-related changes in task-based fMRI activation [Срок оценки: Baseline, 3 months, 6 months]
  • Multi-shell diffusion-tensor imaging [Срок оценки: 3 months]
  • Myelin Mapping with multiparametric MRI [Срок оценки: 6 months]
  • Color Word Interference Test (D-KEFS) [Срок оценки: Baseline, 3 months, and 6 months]
  • Alertness (TAP) [Срок оценки: Baseline, 3 months, and 6 months]
  • Go/No-Go (TAP) [Срок оценки: Baseline, 3 months, and 6 months]
  • Tower Test (D-KEFS) [Срок оценки: Baseline, 3 months, and 6 months]
  • Trail Making Test (D-KEFS) [Срок оценки: Baseline, 3 months, and 6 months]
  • Regensburger Word Fluency Test (RWT) [Срок оценки: Baseline, 3 months, and 6 months]

Критерии участия

Критерии включения

  • Children with CHD: Born with CHD; Underwent cardiopulmonary bypass surgery before the age of one; Children with a genetic disorder or syndromal disorder will be included, if standardized IQ testing with WISC-V can be conducted, and self-rated questionnaires can be filled in; Aged 9 years 0 months to 13 years 11 months (at time of recruitment); Oral informed consent by potential participants (all ages) and parents, as well as written informed consent of parents; EF deficits showing in screening (BRIEF-score ≥ 60)
  • Healthy Controls: Aged 9 years 0 months to 13 years 11 months (at time of recruitment); Oral informed consent by potential participants (all ages) and parents, as well as written informed consent of parents

Критерии исключения

  • Children with CHD: Heart surgery without cardiopulmonary bypass; Children with known large cerebral lesions or injuries, including stroke and severe hypoxic-ischemic encephalopathy with significant neurological sequelae; Insufficient German language skills of the child and parent(s); Attending a separative special educational school (Separative Sonderschulung)
  • Healthy Controls: preterm birth (<36 weeks of gestation); diagnosed with a neurological or substantial developmental disorder (e.g., learning disorder, attention deficit hyperactivity disorder or autism spectrum disorder); Insufficient German language skills of the child and parent(s); Attending a separative special educational school (Separative Sonderschulung)

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Другое

Центры проведения

Швейцария · 1 центр
  • University Children's Hosptial Zurich — Zurich

Идентификаторы

NCT: NCT07692958 · 2026-INV-001 · 10003319

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗