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Набор скоро начнётся NCT07684417

Impact of Short and Mistimed Sleep on Adolescents With ADHD: The Adolescent Attention and Circadian Timing Study

Без фазы С лечением ADHD

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: Aligned sleep extension, Misaligned sleep extension.
Кому может быть актуально
Состояния в реестре: ADHD. Базовые параметры: 13 лет — 17 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
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Impact of Circadian Misalignment for Adolescents With ADHD: Observational and Mechanistic Data

Обзор

Many adolescents go to bed late and wake up early for school. Science is only beginning to understand how sleep schedules can affect them. The investigators are interested in whether changing adolescents' sleep patterns affects their functioning, attention, and how they feel. The investigators are especially interested in the effects of changing both how much sleep adolescents get and when that sleep happens. This study focuses on healthy 13-17-year-olds with ADHD. This study asks adolescents to systematically change their sleeping habits across a 3 week span. The first week, they follow a sleep schedule that fits reasonably well with the schedule they keep when they do not have to wake up early for any specific obligation (e.g., for school). The second week, they spend several nights in a "short sleep" condition, during which they get 6.5 hours in bed per night. The final week, they enter a sleep condition that allows for healthy sleep duration, but with a timing that is randomly assigned to either fit well with their preferred schedule or fit poorly with that schedule. During each week, they and their parents complete measures of their attention and other factors. At the end of each week, they attend an evening session to measure their internal body clock ("circadian phase"), as well as measures of attention and other thinking skills. The goal is to understand whether the benefits of healthy sleep duration depend on the timing of when that sleep occurs.

Вмешательства

  • Поведенческое Aligned sleep extension
    Timing of extended sleep condition is randomly assigned to fit with participant's chronotype
  • Поведенческое Misaligned sleep extension
    Timing of extended sleep condition is randomly assigned to fit poorly with participant's chronotype

Первичные конечные точки

  • Caregiver- and Adolescent-Reported Symptoms of Inattention [Срок оценки: Daily throughout each participant's involvement in the study, up to 3 weeks]
Вторичные конечные точки (6)
  • Caregiver- and Adolescent-Reported Internalizing Symptoms (depression, anxiety) [Срок оценки: Each office visit during the participant's involvement. Office visits are spaced 1 week apart, for up to three visits.]
  • Caregiver- and Adolescent-Reported Emotional Dysregulation [Срок оценки: Each office visit during the participant's involvement. Office visits are spaced 1 week apart, for up to three visits.]
  • Caregiver- and Adolescent-Reported Impulsivity [Срок оценки: Each office visit during the participant's involvement. Office visits are spaced 1 week apart, for up to three visits.]
  • Sleep Period Duration [Срок оценки: Nightly throughout study participation (around 3 weeks)]
  • Inattention [Срок оценки: Twice daily during weeks 2 and 3 of study participation.]
  • Inattention, as objectively measured via the NASA PVT+ application (aka Psychomotor Vigilance Test). [Срок оценки: Four remote administrations: (1) the morning of a predetermined date during Week 2 of study participation; (2) the afternoon of that same Week 2 date; (3) the morning of a predetermined date during Week 3; (4) the afternoon of that same Week 3 date.]

Критерии участия

Критерии включения

  • Ages 13-17 years at time of informed consent/assent
  • Based on semi-structured clinical interview, participants must meet full DSM-5 criteria for ADHD inattentive or ADHD combined presentation.

Критерии исключения

  • Non-traditional school setting (morning-afternoon Monday-Friday).
  • Exclusionary diagnoses. We will exclude adolescents with known intellectual disability, autism spectrum disorder, psychosis, bipolar disorder, or neurologic conditions (e.g., epilepsy), per caregiver-report.
  • Exclusionary sleep disorders. We will exclude adolescents with symptoms of obstructive sleep apnea or periodic limb movement disorder based on published cutoffs on a validated questionnaire.
  • High caffeine intake. To promote adherence to directives not to consume caffeine the day of office visits without withdrawal effects, adolescents with daily intake of >1 coffee or "energy drink" or >2 caffeinated sodas per day based on caregiver- and adolescent-report will be excluded.
  • Unwillingness or inability to take part in study procedures (e.g., visits, prescribed sleep conditions).
  • Medication use or unwillingness to discontinue melatonin and/or stimulant medications during the 3-week study protocol.
  • Refusal to refrain from automobile driving during the sleep restriction condition.
  • "Intermediate" Chronotypes (neither morning larks nor night owls) based on habitual sleep timing on nights when adolescent has no morning obligations such as school or work.

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Факторный дизайн
Маскирование
Открытое
Основная цель
Фундаментальное исследование

Центры проведения

США · 1 центр
  • Cincinnati Children's Hospital Medical Center — Cincinnati

Идентификаторы

NCT: NCT07684417 · R01MH139504 · R01MH139504

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗