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临床试验/NCT05874791
NCT05874791进行中(未招募)不适用

Executive Control Training for Adolescents With ADHD: A Randomized Controlled

Sykehuset Innlandet HF4 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2023年9月15日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
120
试验地点
4
主要终点
Change in Parent-Reported Behavior Rating Inventory of Executive Function - Second Edition (BRIEF-2).

研究概览

简要总结

The goal of this clinical trial is to evaluate an evidence-based, non-pharmacological treatment alternative: Goal Management Training (GMT) for adolescents with Attention-Deficit/Hyperactivity Disorder (ADHD). The main questions we aim to answer are:

  1. Is GMT more effective than Treatment as Usual (TAU) in improving executive functioning in adolescents with ADHD?
  2. Is GMT more effective than TAU in improving emotional health and social functioning in adolescents with ADHD?
  3. Which clinical or cognitive characteristics are associated with treatment response?
  4. Do medication, age, gender, and functional status at intake influence treatment response and long-term outcomes?
  5. Are genetic (e.g. polygenic risk scores) and brain imaging data (e.g. estimates of brain maturation based on structural MRI or resting-state functional magnetic resonance imaging (fMRI) brain connectivity) relevant clinical predictors for treatment response and long-term outcomes?

详细描述

ADHD is characterized by impaired executive functions (EFs). EFs are brain functions that allow us to direct our attention, retain relevant information, and ignore distractions in order to achieve our daily goals. Impairments in EF are associated with poorer academic achievement and vocational functioning, psychopathology symptoms, emotional and social problems, as well as lower quality of life in children and adolescents with ADHD. Furthermore, pharmacological treatment has not been shown to significantly improve EF difficulties, and there is still a considerable knowledge gap regarding the efficacy of non-pharmacological treatment for ADHD. Additionally, the research is often limited by short follow-up periods and few outcome measures.

We propose a randomized controlled trial, comparing a seven-week non-pharmacological cognitive remediation program designed to improve EFs; Goal Management Training (GMT), to treatment-as-usual (TAU) for 120 adolescents with ADHD. The primary outcome is executive function behaviors in the school and home environments (Behavior Rating Inventory of Executive Function 2, parent report). Secondary outcomes include neuropsychological tests, mental health, quality of life, and social deficit symptoms. Participants will be assessed at baseline, after 12 weeks, and 12- and 24 months post-treatment. In addition, we will collect biological samples and brain MRI data in a sub-sample, which will allow us to test whether genetic (e.g. polygenic scores) and brain imaging data collected at baseline (e.g. estimates of brain maturation based on structural MRI or resting-state fMRI brain connectivity) are relevant clinical predictors for treatment response and long-term outcomes. If sample size allows, these analyses will be purely exploratory, and the relevant measures will not be specified in this registration.

The expected main benefit of the described study is to provide evidence-based non-pharmacological treatment to a vulnerable group, potentially improving life-long function and adherence to education, work, and social life.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
12 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Adolescents with a diagnosis of ADHD (ICD-10, DSM-5).
  • Aged 12-18 years. We will include irrespective of concurrent or previous pharmacological treatment.

排除标准

  • Severe depression, suicidality, psychosis, bipolar disorder without stable medication and current substance abuse
  • Organic brain injury or verified neurological disease (3) cognitive or medical impairments that have affected or are affecting the capacity to attend regular school.

结局指标

主要结局

Change in Parent-Reported Behavior Rating Inventory of Executive Function - Second Edition (BRIEF-2).

时间窗: Change from Baseline up to 24 months (Assessed at Baseline, after 12 weeks, after 12 months, and after 24 months).

Rating inventory assessing executive function in daily life. Higher scores indicate greater executive dysfunction. The total score ranges from 86 - 258.

次要结局

  • Change in Parent-Reported Weiss Functional Impairment Rating Scale (WFIRS-P).(Change from Baseline up to 24 months (Assessed at Baseline, after 12 weeks, and after 24 months).)
  • Change in Parent-Reported ADHD Rating scale (ADHD-RS-IV Home).(Change from Baseline up to 24 months (Assessed at Baseline, after 12 weeks, and after 24 months).)
  • Change in Teacher-Reported ADHD Rating scale (ADHD-RS-IV School).(Change from Baseline up to 12 weeks (Assessed at Baseline, and after 12 weeks).)
  • Change in Parent-Rated Pediatric Quality of Life Inventory (PedsQL).(Change from Baseline up to 24 months (Assessed at Baseline, after 12 weeks, and after 24 months).)
  • Change in Teacher-Reported Behavior Rating Inventory of Executive Function - Second Edition (BRIEF-2).(Change from Baseline up to 12 weeks (Assessed at Baseline, and after 12 weeks).)
  • Change in Attention Span task from Cognitive Assessment at Bedside for IPad (CABPad).(Change from Baseline up to 12 weeks (Assessed at Baseline, and after 12 weeks).)
  • Change in Arrow Stroop task from Cognitive Assessment at Bedside for IPad (CABPad).(Change from Baseline up to 12 weeks (Assessed at Baseline, and after 12 weeks).)
  • Change in Children's Global Assessment Scale (CGAS).(Change from Baseline up to 12 weeks (Assessed at Baseline, and after 12 weeks).)
  • Change in Self-Reported Behavior Rating Inventory of Executive Function - Second Edition (BRIEF-2).(Change from Baseline up to 24 months (Assessed at Baseline, after 12 weeks, after 12 months, and after 24 months).)
  • Change in Self-Reported Achenbach System of Empirically Based Assessment (ASEBA).(Change from Baseline up to 24 months (Assessed at Baseline, after 12 weeks, and after 24 months).)
  • Change in Working Memory task from Cognitive Assessment at Bedside for IPad (CABPad).(Change from Baseline up to 12 weeks (Assessed at Baseline, and after 12 weeks).)
  • Change in Parent-Reported Achenbach System of Empirically Based Assessment (ASEBA).(Change from Baseline up to 24 months (Assessed at Baseline, after 12 weeks, and after 24 months).)
  • Change in Self-Rated Pediatric Quality of Life Inventory (PedsQL).(Change from Baseline up to 24 months (Assessed at Baseline, after 12 weeks, and after 24 months).)
  • Change in Goal Attainment Scaling (GAS).(Change from Baseline up to 12 weeks (Assessed at Baseline, and after 12 weeks).)
  • Change in Symbol Digit Coding (Mental and Visuo-Motor Speed) task from Cognitive Assessment at Bedside for IPad (CABPad).(Change from Baseline up to 12 weeks (Assessed at Baseline, and after 12 weeks).)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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