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Learning by Heart: The Effectiveness of an EF Training Program for Pre-schoolers With Critical CHD (LbH)

2026年11月2日 更新者:Andre Rietman、Erasmus Medical Center

The Effectiveness of a Personalized Executive Functioning Training Program for Pre-schoolers With a Critical Congenital Heart Disease

Advances in prenatal and neonatal care have improved outcomes in children with critical congenital heart disease (CCHD). With the increase in survival, neurocognitive problems such as executive functioning (EF) impairments have become more apparent in these children. EF problems have cascading negative effects on a child's development. New insights in EF development suggest that in otherwise physically healthy young children, EF can be improved by training. In a pilot study funded by Stichting Hartekind, the investigators studied the feasibility of a personalized EF training program called 'Kleuter Extra' and the results were promising. Therefore, the current study will investigate the effectiveness of this program in 4-6-year-old children with CCHD. The researchers will also explore interactions between the parent-child relationship and EF development of the child as psychosocial difficulties in these children and their parent(s) and/or caretaker(s) may impact EF-development. If found effective, EF training for children with CCHD will improve their developmental outcome.

研究概览

详细说明

Advances in prenatal and neonatal care have improved outcome in children with critical congenital heart disease (CCHD), with survival rates up to 90%. With the increase in survival, neurocognitive problems and psychological maladjustment have become more apparent in these children, such as impairments in their executive functioning. Executive functioning (EF) is an umbrella-term for several higher-order cognitive processes crucial for self-regulated and goal directed behavior. Frequently postulated components of EF are inhibition, including motor inhibition, and attention, working memory, and cognitive flexibility. Early EF problems often result in emotion regulation difficulties, behavioural problems, social problems, and learning problems, which can lead to diminished functioning in social domains and lower achievement levels in education and employment status. Children with CHD might be rendered even more vulnerable for EF-problems since EF development is embedded within the social context of a child. There is an increasing understanding of how naturally distressing the CHD diagnosis and treatment can be for parents, which can impair the interactions with their child and in turn might negatively impact the child's EF development. Looking at the reciprocal nature of relationships, the child's illness and/or emotional and behavioural problems that may be associated with EF difficulties might negatively impact the parent-child relationship, parenting behaviour and parental wellbeing. However, these relations are poorly understood, especially regarding fathers. A greater understanding of the interplay between biological and psychosocial factors on EF-development is needed to promote optimal developmental outcomes for these vulnerable children.

New insights suggest that EF can be improved by training. Due to neural plasticity, the window for effective training seems to be between the ages of two and six years. After this time frame, improvements in EF may not retain after training or not generalize to off-task functions. Current EF training programs are not personalised ('adaptive') but offer the same program regardless of the specific child's EF dysfunctions, which may explain their limited effects. There is presently no effective EF training program for children with CHD.

In a pilot study funded by Stichting Hartekind, the researchers investigated the feasibility of a personalised EF training program called 'KleuterExtra' in 4-6 year old children with critical CHD. Within a week, 31 children were (self-) referred for the study, indicating a great clinical need. Directly after training, children showed clinically relevant improvement on the specific EFs targeted in training, with Cohen's d effect sizes ranging from 0.19 to 2.41 (>1.00 on 5 out of 9 tasks). Improvement was also found in untrained EFs and tasks that combined multiple EFs, indicating a generalization effect. Parents and teachers spontaneously reported positive results in daily life. Based on these promising results, the investigators designed the current randomized, controlled study to test the effectiveness of this training program in pre-schoolers with severe CHD.

Given the above, the investigators designed this study to investigate the effectiveness of a tailored EF training program for preschoolers with CCHD. Secondary aim was to explore interactions between the parent-child relationship and the EF development of the child. If found effective, EF training for children with CCHD will improve their developmental outcome.

研究类型

介入性

注册 (实际的)

103

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Provincie Groningen
      • Groningen、Provincie Groningen、荷兰、9713GZ
        • University Medical Center - Beatrix children's hospital Groningen
    • Rotterdam
      • Rotterdam、Rotterdam、荷兰、3015CN
        • Erasmus Medical Center Sophia Children's Hospital
    • Utrecht
      • Utrecht、Utrecht、荷兰、3584EA
        • University Medical Center - Wilhelmina children's hospital Utrecht

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

4年 至 6年 (孩子)

接受健康志愿者

不

有资格学习的性别

全部

描述

In order to be eligible to participate in this study, a child must meet all of the following criteria:

  • Aged 4.0 - 5.11 years upon inclusion OR aged 6.0-6.11 years and still attending kindergarten (group 1-2 of the Dutch school system)
  • Required CHD surgery in the first six months of life (with or without cardiopulmonary bypass or ECMO) or a cyanotic CHD that required surgery in the first 12 months of life
  • IQ estimated > 55 (no moderate to severe intellectual disability)
  • Diminished EF based on a below average score on any of the subtests of the 'KleuterExtra' test battery (≤ 21 percentile) at t = 0
  • Sufficient comprehension of the Dutch language by the child to be able to participate in the EF test battery and the EF training program.

In order to be eligible to participate in this study, the parent(s) must meet the following criteria:

- Sufficient comprehension of the Dutch language to understand the study information and to be able to fill out the Dutch questionnaires.

Exclusion Criteria:

  • Children with severe brain damage (estimated IQ < 55)
  • Genetic syndromes known to directly affect cognitive performance (e.g. Down syndrome)
  • Children with severe psychiatric disorders upon inclusion that require treatment first, such as a posttraumatic stress disorder, separation anxiety disorder, or reactive attachment disorder.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Intervention group

The participants allocated to the intervention group will receive the personalised training program 'KleuterExtra', developed by dr. Lex Wijnroks from Utrecht University. All parents will receive the book 'Speels Brein' ('Playful Brain') and an age-appropriate addition for preschoolers to this book.

The intervention was described in the included arm/group explanation.

无干预:Control group

As described, the parents of the control group will also receive the book 'Speels Brein' ('Playful Brain') and the age-appropriate addition for preschoolers to this book.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Kleuter Extra test battery
大体时间:9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

The primary endpoint is a single composite score on the 'KleuterExtra' EF test battery, calculated as the mean z-score (mean = 0, SD = 1) of the ten tasks of the test battery. The composite score has no fixed minimum or maximum, and a higher score indicates a better outcome.

9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

次要结果测量

结果测量
措施说明
大体时间
EF functioning
大体时间:9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

Scores on the 10 individual tasks of the 'KleuterExtra' test battery, four EF domain scores (inhibition, attention, working memory, cognitive flexibility), and an integrated EF score (based on task 'Head-Toes-Knees-Shoulders'; HTKS).

Raw task scores:

  • 'Pencil Tap': 0 to 100
  • 'Go/No go animals': 0 to 20
  • 'Statue task': 0 to 30
  • 'Visual search task': 0 to 18
  • 'Sustained attention': 0 to 30
  • 'Corsi blocks': 0 to 15
  • 'Dots': 0 to 74
  • 'Digit Recall': 0 to 54
  • 'Three of a Kind': 0 to 68
  • 'HTKS': 0 to 52

A higher score indicates a better outcome for all tasks, except 'Go/No go animals' (reverse scored). Raw scores are converted to z-scores (mean = 0, SD =1) for analysis. A higher z-score indicates a better outcome. Domain scores are calculated as the mean z-score of the tasks within each domain.

9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.
Information processing
大体时间:9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

Cognitive Proficiency Index of the WPPSI-IV-NL: index score (mean = 100, SD =15, range 40-160), and a higher score indicates a better outcome. The CPI is based on four subtests (scaled scores 1-19):

  • subtest 'Picture Memory'
  • subtest 'Zoo Locations'
  • subtest 'Bug Search'
  • subtest 'Cancellation'
9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.
Executive functioning in daily life - completed by the parent(s)
大体时间:9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

Behavior Rating Inventory of Executive Function - Preschool Version questionnaire (BRIEF-P): t-scores range from 20-80, higher scores indicate worse outcome. The three calculated main indexes (inhibitory self-control, flexibility, and metacognition) will be used for the current trial.

9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.
Behavioral and emotional difficulties of the child - completed by the parent(s)
大体时间:9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

Child Behavioral Checklist questionnaire 1,5 - 5 years old (CBCL): t-scores range from 50-100, higher scores indicate worse outcome. The three overall domains (internalizing behavior, externalizing behavior, and the total sum of problems) will be used for the current trial.

9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.
Quality of the child's life - completed by the parent(s)
大体时间:9 weeks after baseline, additional measures at 6 months and 12 months after baseline.

Preschool Children Quality of Life questionnaire (TAPQOL): scale scores range from 0 - 100, higher score indicates better outcome. All twelve scales will be used for the current trial: stomach problems, skin problems, lung problems, sleeping problems, appetite, problem behavior, positive mood, anxiety, liveliness, social functioning, motor functioning, and communication.

9 weeks after baseline, additional measures at 6 months and 12 months after baseline.
Emotional distress parent - completed by the parent(s)
大体时间:9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

Depression, Anxiety, Stress Scale (DASS-21): subscale scores (depression, anxiety, stress) range from 0-21 and the total score ranges from 0-63. A higher score indicates worse outcome. These four scales will be used for this trial.

9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.
Parental trauma
大体时间:9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

PCL-5 questionnaire ('PCL-5' is the title, scores range from 0-80, higher score indicates worse outcome)

9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.
Parenting behavior questionnaire - completed by the parent(s)
大体时间:9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

Parenting Behavior questionnaire (PABI; Dutch title 'Vragenlijst over opvoedgedrag'): T-scores range from 20-80. The three adaptive domains (warmth, structure, and autonomy), and three maladaptive domains (hostility, coercion, and excessive protection) will be used for the current trial. Higher scores indicate a better outcome on the adaptive domains, and a worse outcome on the maladaptive domains.

9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.
Child demographics: schooling - completed by the parents
大体时间:Baseline. Changes are recorded at 9 weeks, 6 months, and 12 months after baseline.

Additional support in school, type, being held back a year (qualitative data, designed by the study group)

Baseline. Changes are recorded at 9 weeks, 6 months, and 12 months after baseline.
Behavioral and emotional difficulties teacher's perspective
大体时间:9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

Teacher's Report Form questionnaire (C-TRF): t-scores range from 50-100, higher scores indicate worse outcome. The three overall domains (internalizing behavior, externalizing behavior, and the total sum of problems) will be used for the current trial.

9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.
Executive functioning child in daily life teacher's perspective
大体时间:9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

Behavior Rating Inventory of Executive Function questionnaire - teachers (BRIEF-P); t-scores range from 20-80, higher scores indicate worse outcome.

9 weeks after baseline. Additional measures at 6 months and 12 months after baseline.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:André Rietman、Erasmus Medical Center
  • 首席研究员:Renske Schappin、Erasmus Medical Center

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2024年5月1日

初级完成 (实际的)

2025年10月29日

研究完成 (估计的)

2026年11月30日

研究注册日期

首次提交

2023年12月12日

首先提交符合 QC 标准的

2024年2月12日

首次发布 (实际的)

2024年2月20日

研究记录更新

最后更新发布 (实际的)

2026年11月4日

上次提交的符合 QC 标准的更新

2026年11月2日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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