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临床试验/NCT02897362
NCT02897362已完成不适用

Sleep Dysfunction and Neurocognitive Outcomes in Adolescent ADHD

Duke University1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2016年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
62
试验地点
1
主要终点
Objective sleep assessment

研究概览

简要总结

This study seeks to characterize sleep physiology in adolescents with and without Attention deficit hyperactivity disorder (ADHD) and its relationship to differential neurocognitive and clinical outcomes within these groups.

详细描述

This project will involve recruitment of 30 adolescents with ADHD and a control group of 30 healthy adolescents without psychiatric diagnoses. Participants will participate in 3 phases: Screening visit, Washout/In-Home Sleep Study, and Neurocognitive Assessment visit. To ensure consistency in sleep schedules, the three nights of the sleep study will occur on weeknights during the school year. The neurocognitive assessment will occur during the afternoon following the final night of sleep assessment.

The 2-hour screening visit will be conducted at the Duke ADHD Clinic at 2608 Erwin Road, Pavilion East, Suite 300, Durham, NC 27705. During the screening visit, participants will undergo screening to evaluate eligibility for the study.

Eligible participants will enter the 48-hour Washout from stimulant medication (if applicable) and/or a 7-day washout from melatonin (if applicable). Following this washout, subjects will enter a 3-night Sleep Study Phase (At Home). Subjects not taking stimulant medication or melatonin will initiate 3 consecutive nights of ambulatory (in-home) PSG recording, beginning on the a Monday evening within 4 weeks of the screening visit. Subjects will be instructed to maintain usual sleep routines/behaviors for all study nights. In addition, subjects will be asked to complete a "sleep diary" each morning.

If subject is currently taking stimulant medication, they will be instructed to initiate a 48-hour washout period. If subject is currently taking melatonin, they will be instructed to initiate a 7-day washout period. Subjects will be instructed to discuss this option with their prescribing physician prior to initiating the study.

Subjects will be asked to return for a three hour neurocognitive assessment on the afternoon directly following the final night of the sleep study. In order to reduce interference with school attendance, this visit will be scheduled in the afternoon. Subjects will take breaks throughout the assessment.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
13 Years 至 17 Years(Child)
性别
All
接受健康志愿者
是

入选标准

  • •Male or Female
  • •Between the ages of 13-17 years, inclusive;
  • •Free from significant medical/psychiatric conditions
  • •Cognitive functioning > 80 as assessed by the KBIT-II
  • •Willingness to comply with all study requirements; and
  • •Ability of child and parent/guardian to communicate verbally and in written form in English.
  • •Inclusion for the ADHD group only:
  • •Confirmed diagnosis of ADHD, any subtype as determined by the MINI-KID
  • •Willingness to delay/suspend medication use for the 4-day duration of the study and 2 days prior to the sleep study phase.

排除标准

  • •History of chronic/significant medical condition
  • •Use of prescription medications for ADHD during the 2-day washout and/or 4-day study
  • •Current prescribed use of any other psychotropics, including non-stimulant medications for ADHD
  • •Current substance abuse or dependence or history within the last 6 months
  • •Estimated IQ < 80 as assessed by the KBIT-II
  • •First degree relative with psychosis or bipolar disorder;
  • •Parent/Guardian or child unable to communicate verbally and in written form in English; and
  • •Unable to comply with study requirements or otherwise unsuitable for participation in the opinion of the principal investigator
  • •Exclusion for the ADHD group only:
  • •Meets criteria for any other Axis I Disorder (determined by the MINI-KID) besides ADHD or Oppositional Defiant Disorder (ODD)
  • •Exclusion for the HEALTHY CONTROL group only:
  • •Meets criteria for any Axis I Disorder

结局指标

主要结局

Objective sleep assessment

时间窗: 3 consecutive nights

Ambulatory polysomnographic measures of total sleep time, sleep onset latency, wake after sleep onset, and EEG spectral dynamics.

次要结局

  • Neurocognitive assessment(1 day)
  • Executive functioning as measured by neurocognitive assessment(1 day)

研究者

发起方
Duke University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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