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Идёт набор NCT06737224

The Impact of a 48-hour Fast with or Without Exercise on Immune Cell Metabolism and Glycemic Control in Healthy Active Adults

Без фазы С лечением Fasting Immune Function Glucose Tolerance

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: Fasting + Exercise (FAST+EX): fasting + exercise condition, Fasting only (FAST): Non-exercise fasting condition.
Кому может быть актуально
Состояния в реестре: Fasting, Immune Function, Glucose Tolerance. Базовые параметры: 19 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
Канада
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

The Impact of a 48-hour Fast with or Without Exercise on Immune Cell Function, Bioenergetics, and Glycemic Control in Healthy Active Adults: a Randomized Crossover Trial

Обзор

Many individuals engage in fasting for its purported health benefits but the effects of fasting on immune cell and whole body metabolism are not well understood in humans. Moreover, how exercising during a prolonged fast impacts immunometabolic outcomes is unclear. This study will determine how a 2 day fast - performed with or without daily exercise - impacts immune cell bioenergetics, immune cell function, and whole-body glycemic control in healthy active individuals.

Подробное описание

Participants will perform two, 48-hour fasts separated by 5 days while wearing a continuous glucose monitor to measure glycemic responses. The order of the trials will be randomized for each participant. The two trials will include an exercise condition (FAST+EX) and a control, non-exercise condition (FAST). During the FAST+EX trial, participants will perform 60 minutes of cycling on each of the two days of the fast. Each bout of exercise will be 60 minutes in duration and consist of 50 minutes of cycling at 60% of predicted heart rate reserve (HRR) followed by 5 x 1-minute intervals at 90% of predicted HRR with 1-minute of passive recovery between each interval. During the FAST trial, participants will be asked to refrain from any structured exercise during the days of the fast. To start the trial, participants will arrive at the lab following an overnight fast. They will consume a standardized meal replacement (Ensure Plus Calories) and blood will be drawn 2 hours post-ingestion. Participants will come to the lab 24 and 48 hours later for subsequent blood draws prior to breaking their fast with the same standardized meal replacement. Another blood sample will be taken 2 hours post-prandial. Participants will be asked to replicate food consumption in each condition for the 24-hour period after they break their fast, and consume the same standardized meal replacement on the morning following the completion of each fast to measure free-living glycemic control 24-hours after a fast performed with or without exercise. There will be a five-day wash out period in between the completion of both trials for all participants.

Вмешательства

  • Другое Fasting + Exercise (FAST+EX): fasting + exercise condition
    Participants will complete a 48-hour fast. One hour of exercise will be performed on each morning of the fast.
  • Другое Fasting only (FAST): Non-exercise fasting condition
    Participant will complete a 48-hour fast. No structured exercise will be performed during each of the fasting days.

Первичные конечные точки

  • Monocyte mitochondrial respiration [Срок оценки: Baseline and 48 hours]
Вторичные конечные точки (11)
  • Alteration in immune cell functions [Срок оценки: Baseline and 48 hours]
  • Change in glucose tolerance [Срок оценки: Baseline, after 48 hours of fasting, and 24 hours after breaking the fast in free-living condition)]
  • Blood pressure [Срок оценки: Baseline, 24 hours into the fast, and at the end of the fast (48 hours)]
  • Rate and level of ketosis [Срок оценки: Baseline, 24 hours and 48 hours during fasting]
  • Compensatory movement behaviour [Срок оценки: During and 48 hours after the fast]
  • Hunger sensation [Срок оценки: At baseline, 12:00, 18:00 during the first and second day of the fast.]
  • Sleep quality [Срок оценки: Baseline the morning before starting the fast, after 24 hours of fasting, and again after 48 hours of fasting.]
  • Affect during exercise [Срок оценки: Before, during (e.g., at 10, 20, 30, 40, and 50 minutes as well as during intervals 1,2,3,4, and 5 at the end of the intervals as well as during the passive recovery) and following the two exercises conditions (post 5 minutes in a seated position).]
  • Remembered Enjoyment [Срок оценки: 10 minutes after each exercise session.]
  • Rate of perceived exertion [Срок оценки: During both exercise sessions at 10, 20, 30, 40, and 50 minutes as well as during intervals 1, 2, 3, 4, and 5 at the end of the intervals.]
  • Glucose homeostasis [Срок оценки: During and 24 hours after both condition]

Критерии участия

Критерии включения

  • Aged between 19 and 35 years.
  • Physically active (engaging in ≥150 minutes of weekly moderate to vigorous physical activity).

Критерии исключения

  • History of cardiometabolic diseases or inflammatory diseases (e.g., chronic obstructive pulmonary disease (COPD), rheumatoid arthritis, cardiovascular disease).
  • Individuals currently following a ketogenic diet, low-calorie diet, periodic fasting regimen, or consuming ketogenic supplements (e.g., exogenous ketone drinks).
  • Cigarette/vaping smoking.
  • Physical limitation that will impair the ability of the participant to perform exercise.
  • Individuals having a body mass index (BMI) over 30 kg/m2.
  • Cancer diagnosis in the past 5 years.
  • Taking anti-inflammatory drugs (e.g., ibuprofen, aspirin, naproxen).
  • Being unable to read or communicate in English.

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
Простое слепое
Основная цель
Другое

Центры проведения

Канада · 1 центр
  • University of British Columbia Okanagan Campus — Kelowna

Идентификаторы

NCT: NCT06737224 · H24-01732

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗