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Идёт набор NCT07578103

Effect of Dairy Protein Yogourt vs Plant-based Yogourt on Body Weight, Body Composition, Bone Health and Gut Microbiota

Без фазы С лечением Body Composition Changes Body Weight Change Metabolic Health Bone Metabolism

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: Dairy yogurt, Plant based yogurt, No yogurt.
Кому может быть актуально
Состояния в реестре: Body Composition Changes, Body Weight Change, Metabolic Health, Bone Metabolism. Базовые параметры: от 40 лет · Женщины.
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

A New Focus on Protein and the Gut Microbiota to Explain Health Benefits of Dairy Foods

Обзор

The consumption of an adequate quantity of protein in the diet is essential to maintain a healthy body composition and functioning. It is also well established that all proteins are not equal regarding their ability to promote health benefits. Recently, we have innovated in that matter by showing that under the context of high intake of dietary fat, the dairy protein casein was more effective than a mix of proteins representative of a western diet to prevent body weight gain and insulin resistance. This was explained in part by modifications of the gut microbiota. This finding represents the main conceptual basis of the present research program that is aimed to determine the impact of dairy protein from yogurt compared to a plant-based equivalent on body composition indicators including muscle mass and bone mineral density, in relation to the profile of the gut microbiota, the production of newly discovered protein-derived metabolites, and markers of metabolic health. This program will include a human and an animal component requiring the testing of these variables before and after a standardized intervention. The human component will be a clinical study consisting of a 12-week diet-based weight loss intervention in postmenopausal overweight women being randomly assigned to one of the three following groups: yogurt, plant-based yogurt, or kept on diet without supplements. The animal experimentation will permit to causally determine the implication of the gut microbiota in the protein effects following transfer of the human bacteria to germ free mice and validate the benefits seen in humans. It is anticipated that these two complementary investigative approaches will allow a thorough documentation of the impact of fermented dairy protein on body composition and functioning, a better understanding of the underlying mechanisms, and the identification of new biomarkers to better appreciate related health benefits.

Вмешательства

  • Пищевая добавка Dairy yogurt
    Dairy yogurt: two serving daily
  • Пищевая добавка Plant based yogurt
    Plant based yogurt: two servings daily
  • Пищевая добавка No yogurt
    No yogurt: zero serving yogurt

Первичные конечные точки

  • Change in bone health [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in bone health [Срок оценки: At baseline and at the end of the intrevention (12 weeks)]
  • Change in gut microbiota [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in gut microbiota function [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
Вторичные конечные точки (12)
  • Change in body weight [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in anthropometric measures [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in anthropometric measure [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in body composition [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in skeletal muscle health [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in skeletal muscle health [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in skeletal muscle health [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in Resting Metabolic Rate (RMR) [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in Appetite and Satiety [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in Appetite and Satiety [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in Eating behaviors [Срок оценки: At baseline and at the end of the intervention (12 weeks)]
  • Change in glycemia [Срок оценки: At baseline and at the end of the intervention (12 weeks)]

Критерии участия

Критерии включения

  • Postmenopausal women (absence of menstruation for at least 1 year and FSH > 40 IU/L)
  • BMI between 27.0 and 39.9 kg/m²
  • Sedentary or moderately active

Критерии исключения

  • Body weight change greater than 5 kg in the 3 months preceding the study
  • Currently dieting or following specific dietary patterns
  • Previous or planned bariatric surgery
  • Food allergies or intolerances (particularly dairy proteins and lactose)
  • Serious or problematic health conditions (e.g., renal insufficiency, diabetes, Cushing's disease, Paget's disease, parathyroid disorders, inflammatory bowel disease, uncontrolled thyroid disease, etc.)
  • Fracture within the past year
  • Hormone therapy
  • Medications affecting bone metabolism (e.g., osteoporosis treatments, anti-estrogen therapy for breast cancer, epilepsy treatments)
  • Antibiotic use within the 6 months preceding the study
  • Use of probiotic supplements (capsules)
  • More than two alcoholic drinks per day
  • Smoking
  • Drug abuse

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

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Профилактика

Центры проведения

Канада · 1 центр
  • INAF, Université Laval — Québec

Идентификаторы

NCT: NCT07578103 · PROYO 2022-108

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗