Nighttime Synchrony of Your Nutrition and Circadian Health
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: Central Clock Misalignment, Peripheral Misalignment.
- Кому может быть актуально
- Состояния в реестре: Sleep, Metabolism Changes, Circadian Rhythm, Lifestyle Factors. Базовые параметры: 18 лет — 35 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 →
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Официальное название
Nighttime Synchrony of Your Nutrition and Circadian Health: The N-Sync Study
Обзор
Sleep is an important factor for overall health. This study will see how different light exposure patterns and food intake impact a person's metabolism (how the body breaks down food) when sleeping is reduced. Participants will attend 6 to 8 in-person visits to the study clinic, including three overnight stays. People will complete surveys and medical tests. The study will last about 4 to 6 months.
Подробное описание
This study is a randomized in-lab, cross-over trial. Each participant will complete all three arms in either condition order #1 (A-B-C) or order #2 (A-C-B). Each arm will consist of 5 nights of experimental sleep restriction followed by a constant routine protocol for assessment of 24-h rhythms. Sleep restriction in the three arms will occur under the following conditions: (A-control condition) Sleep Restriction with Central and Peripheral Alignment; (B) Sleep Restriction with Central Clock Misalignment; and (C) Sleep Restriction with Peripheral Misalignment. Prior to enrollment participants will complete a comprehensive medical history and clinical overnight sleep disorders screening. Baseline consists of a \~2-week ambulatory real-world monitoring segment that will occur immediately prior to each in-lab sleep restriction condition. Following the 5 days of sleep restriction in each arm, participants will complete an intravenous glucose tolerance test to analyze insulin sensitivity, prior to completing the constant routine.
Вмешательства
- Поведенческое Central Clock Misalignment
Light exposure will be dimmed during the first 4 hours of scheduled wakefulness, with bright light exposure during the nighttime hours of extended wakefulness. - Поведенческое Peripheral Misalignment
Most daily calories will be given later in the day to shift eating patterns toward the nighttime hours.
Первичные конечные точки
- Insulin Sensitivity [Срок оценки: Immediately following the 5-day sleep restriction segment]
- Internal Circadian Misalignment (Uridine and Isobutyryl-L-carnitine) [Срок оценки: During the constant routine, following the 5-day sleep restriction segment]
Критерии участия
Критерии включения
- Age: 18-35 years old; equal numbers of men and women
- Body Mass Index (BMI): 18.5-24.9 kg/m2
- Sleep Habits: habitual self-reported average total sleep time (TST) 7-9 hours per night for prior 6 months
Критерии исключения
- Clinically diagnosed sleep disorder or apnea hypopnea index (AHI) ≥5
- Evidence of significant organ system dysfunction or disease (e.g., heart disease, diabetes)
- Fasting plasma glucose ≥100 mg/dL
- Major psychiatric illness (e.g., major depressive disorder)
- Cancer that has been in remission less than 5 years
- History of shift-work in prior year
- Weight change >5% of body weight over prior six months
- Currently following a weight-loss program
- Menopause
- Pregnant/nursing
- Greater than 5-day variation in menstrual cycle length month-to-month
- Currently smoking
- Alcohol intake >14 drinks/week or >3 drinks/day.
- Use of prescription medications (except oral contraceptives) within one month prior to or during in-lab visits.
- Consumption of illegal drugs or >500mg per day of caffeine.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Да
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Перекрёстный дизайн
- Маскирование
- Тройное слепое
- Основная цель
- Фундаментальное исследование
Центры проведения
США · 1 центр
- College of Health Research Complex - University of Utah, Salt Lake City 84112 — Salt Lake City
Идентификаторы
NCT: NCT07329283 · 185590