ACTRN12623001147673尚未招募4 期
Effectiveness of methylphenidate in children with co-occurring attention-deficit/hyperactivity disorder (ADHD) and autism - MICAA Trial
Professor Katrina Williams0 个研究点目标入组 40 人开始时间: 2023年11月6日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 6 Years 至 15 Years(—)
- 性别
- All
入选标准
- •Each participant (child) must meet all the following criteria to be enrolled in this trial:
- •- Is between the ages of 6 - 15 years at the time of enrolment.
- •- Has a clinical diagnosis of ADHD and of ASD.
- •- Has been taking a stable dose of MPH-IR (i.e. Ritalin 10) for one month prior to trial enrollment.
- •- Parent has signed and dated an informed consent form.
排除标准
- •Exclusion criteria will include any of the following:
- •- Inability to read or speak sufficient English for parent/guardian to complete assessment tasks.
- •- Is currently taking a medication other than MPH-IR (i.e. Ritalin 10) for the purpose of treating ADHD symptoms.
- •- Unable to swallow capsules.
- •- Has major illness or disability, including but not limited to: epilepsy, major head injury, Fragile X Syndrome or Williams Syndrome, Foetal Alcohol Spectrum Disorder (FASD) or Neonatal abstinence syndrome.
- •- Is known to be pregnant.
- •- Research team is not confident the child has both an ADHD and ASD diagnosis.
- •- Parent/guardian does not consent to contact with the clinician and school.
- •- Is deemed by their treating clinician (psychiatrist/paediatrician/GP) to be medically unfit for trial participation.
- •- Child’s school is unwilling to participate in outcome assessments.
研究者
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