GLycaemic Outcomes With Whey Protein in ageING
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: Glycaemic control with whey protein, Glycaemic control with different doses of whey protein.
- Кому может быть актуально
- Состояния в реестре: Type 2 Diabetes. Базовые параметры: 75 лет — 90 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
- Великобритания
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Не всё понятно в терминах? Прочитайте наш гид для пациентов →
Официальное название
Whey Protein Dose-response Effect on Daily Glycaemic Excursions in Very Old Individuals With Type 2 Diabetes
Обзор
The goal of this placebo-controlled, partial crossover design study is to identify the impact of consuming whey protein before meals on free-living glucose control in older adults living with type 2 diabetes. The primary specific objective is to determine the effect of a thrice daily whey protein pre-meal supplementation at two doses, on glucose excursions over a 7-day free-living period in adults aged 75-90 years of age, living with type 2 diabetes, compared with a non-protein placebo. Participants will consume the whey protein and placebo for 7 days each, before each meal. All participants will consume the placebo and one of two doses of whey protein, in a randomised order.
Подробное описание
Within the study, the researchers will look at the effect of supplemental whey protein at moderate and low doses in comparison to each other and a protein-free placebo on glycaemic control in older adults aged between 75-90 years of age, living with type 2 diabetes.
Glycaemic control (glucose excursions) will be monitored under free-living conditions over a 7-day period using continuous glucose monitors (CGMs). Participants will be randomised to consume one of the two whey protein doses as well as the protein-free placebo on a separate 7-day period. The order of consuming whey protein or the protein-free placebo will be randomised and counterbalanced. This study is under the evidence that in younger people living with type 2 diabetes, a moderate dose of whey protein improves glucose time in range and lessens extreme postprandial glucose excursions.
Participants will be free to consume their typical diet over this period, where the researchers will provide a diet diary for participants to enter in all foods and drinks they consume over this time period, as well as document the ingestion of the supplement before each main meal.
During an acute feeding period on the first ingestion of each supplement (start of each 7-day phase), the researchers will evaluate rates of gastric emptying, glucose and insulin concentrations and hormonal appetite markers through blood draws, as well as perceived appetite responses through visual analogue scales. This will be in a research kitchen where participants will consume the supplement and a controlled mixed meal afterwards to monitor excursions in appetite response and glycemia. The researchers will also investigate the impact of pre-meal protein feeding on renal markers following each 7-day phase via urine collection.
Вмешательства
- Пищевая добавка Glycaemic control with whey protein
Comparing pre-meal supplementation of whey protein to protein-free placebo. - Пищевая добавка Glycaemic control with different doses of whey protein
Comparing pre-meal supplementation of moderate whey protein to a low dose of whey protein.
Первичные конечные точки
- Measurement of changes in free-living glycaemic control [Срок оценки: 7 days, two occasions]
- Changes in postprandial glucose concentrations in blood [Срок оценки: 4 hours, two occasions]
- Concentrations of insulin postprandially in blood [Срок оценки: 4 hours, two occasions]
Вторичные конечные точки (7)
- Concentrations of amino acids postprandially in blood [Срок оценки: 4 hours, two occasions]
- Concentrations of postprandial appetite hormones [Срок оценки: 4 hours, two occasions]
- Rate of gastric emptying [Срок оценки: 4 hours, two occasions]
- Changes in renal function markers after each 7-day phase [Срок оценки: 2 urine samples, 2 occasions]
- Assessment of nitrogen balance from urine after each 7-day phase [Срок оценки: 24 hours, two occasions]
- Measurement of blood lipid concentration [Срок оценки: 1 blood draw (obtained from the first blood draw as part of 4 hour visit)]
- Optional qualitative assessment of perceptions to supplementation [Срок оценки: 60 minutes]
Критерии участия
- Male or female
- 75-90 years old
- Type 2 Diabetes (confirmed with glycated haemoglobin (HbA1c) >6.5% in clinic or in SportExR)
- Stable body mass (body mass index (BMI) ≤40kg/m2)
- Generally healthy, assessed via a General Health Questionnaire (GHQ)
- Some residual beta-cell activity (confirmed with urine test on induction)
- Normal or moderately increased albuminuria (needs to be below 300mg/g)
- Normal, mildly or moderately decreased glomerular filtration rate (GFR) (needs to be above 45ml/min/1.732).
- Able and willing to attend SportExR a total of 5 times: 1 induction and 2 testing visits and 2 return check-up visits.
Критерии исключения
- <75 years old and over 90 years of age
- Currently on fast-acting insulin therapy (i.e., Humalog)
- Confirmed uncontrolled diabetes (HbA1C >10% or 85mmol/mol).
- Currently on GLP-1 therapy
- Habitual smoker or vaper
- Veganism
- Lactose or dairy intolerance
- Coeliac or gluten intolerance
- History of gastrointestinal disease
- Experienced a hyperglycaemic or hypoglycaemic event requiring treatment in the past 12 months
- Recent Ischemic stroke (<3 months).
- Use of anticoagulants (e.g. warfarin, rivaroxaban)
- Considered unwilling or unable to comply with the study protocol requirements by the research team
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
Великобритания · 2 центра
- School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham — Birmingham
- Heartlands Hospital — Birmingham
Идентификаторы
NCT: NCT07285811 · RG_24-052