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Идёт набор NCT05740254

Early vs. Late Time-Restricted Eating in Adolescents With Obesity (EL TREA)

Без фазы С лечением Pediatric Obesity Time Restricted Feeding Time Restricted Eating

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: Early Time Restricted Eating, Late Time Restricted Eating.
Кому может быть актуально
Состояния в реестре: Pediatric Obesity, Time Restricted Feeding, Time Restricted Eating. Базовые параметры: 12 лет — 21 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 →

Обзор

Determine the effectiveness of how limiting the time you eat within an early or late eating window and fasting for remainder of the day will impact weight loss and body mass index (BMI).

Подробное описание

In adults, there is growing evidence that early TRE is more effective in improving metabolic outcomes than other forms of TRE, however it is unclear whether adolescents will be able to adhere to such recommendations. Hence, in the present study we propose a 24-week, 2-arm, parallel randomized pilot trial in 100 adolescents (age 13-18 years, all gender expressions, anticipate 65% Latino) with obesity, to test the preliminary efficacy of early vs. late TRE on glycemic profiles, weight loss, and body composition. We hypothesize that, among adolescents who can adhere to the meal timing recommendations, early TRE will result in greater improvement in metabolic endpoints than late TRE. We will test the hypothesis with 3 specific aims: Aim 1: Test the effect of early vs. late TRE on glycemic profiles and β-cell function. Aim 2: Test the effect of early vs. late TRE on obesity and body composition, and cardiometabolic risk factors. Aim 3: Test the effect of early vs. late TRE on exploratory outcomes including sleep, physical activity, and dietary intake to explore how meal timing may influence occurrence, timing, and distribution of sleep and movement as well as dietary intake and caloric distribution. This study is the first study evaluating the effectiveness of early vs. late TRE in adolescents with obesity at risk for diabetes.

Вмешательства

  • Поведенческое Early Time Restricted Eating
    Early Time Restricted Eating 7 AM to 3 PM
  • Поведенческое Late Time Restricted Eating
    Late Time Restricted Eating 12 PM to 8 PM

Первичные конечные точки

  • Mean change in weight in excess of the 95th percentile at week 24 compared to baseline [Срок оценки: week 24]
Вторичные конечные точки (5)
  • Mean change in total body fat mass as measured on DEXA scan at week 24 compared to baseline [Срок оценки: week 24]
  • Mean change in percent time in range as captured on contiguous glucose monitor at week 24 compared to baseline [Срок оценки: week 24]
  • Mean change in hemoglobin A1c at week 24 compared to baseline [Срок оценки: week 24]
  • Mean change in ALT at week 24 compared to baseline [Срок оценки: week 24]
  • Mean change in systolic and diastolic blood pressure at week 24 compared to baseline [Срок оценки: week 24]

Критерии участия

Критерии включения

  • 12-21 years with obesity (BMI>95th percentile)
  • participant must be willing and able to adhere to the assessments, visit schedules, and eating/fasting periods
  • baseline eating window greater than 12 hours.

Критерии исключения

  • diagnosis of Prader-Willi Syndrome, brain tumor, or diabetes serious intellectual disability
  • previous diagnosis or subthreshold symptoms of an eating disorder (anorexia nervosa, bulimia nervosa, binge-eating disorder)
  • parent/guardian-reported physical, mental of other inability to participate in the assessments
  • previous bariatric surgery
  • current participation in other interventional weight loss studies.

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Лечение

Центры проведения

США · 1 центр
  • Children's Hospital Los Angeles — Los Angeles

Идентификаторы

NCT: NCT05740254 · CHLA-22-00395

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗