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临床试验/NCT03625245
NCT03625245已完成不适用

Pilot Study to Evaluate the Satiating Effect of Enriched Functional Yogurts With Soluble Fibre or Vegetable Protein in a Group of Healthy Overweight Subjects

Instituto de Investigación Hospital Universitario La Paz1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2018年5月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
12
试验地点
1
主要终点
Change from Baseline Satiety Hunger Assessment

研究概览

简要总结

The purpose of this study is to evaluate the satiating effects of different functional yogurts enriched with soluble fiber or vegetable protein on overweight subjects (BMI ≥25 and <30 kg / m2).

Some studies have shown the contribution of high-fiber foods in the reduction of the cardiovascular risk. On the other hand, protein consumption could have a greater satiety potential compared to other macronutrients.

详细描述

A randomized, cross-over and double-blind pilot study with 3 study arms is being performed to evaluate the satiating properties of different functional enriched yogurts with soluble fiber or vegetable protein in a group of healthy overweight subjects.

The investigators included 12 participants (6 men and 6 women) between 18 and 55 years (BMI ≥25 and <30 kg / m2). All volunteers will be randomized into 3 study groups, and participants will receive the 3 different study products in order during the 3 experimental phases.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
Double (Participant, Investigator)

盲法说明

Double Blind (Participant and Investigator)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Men and women from 18 to 65 years old.
  • •Body Mass Index (BMI) ≥25 and <30 kg/m
  • •Adequate cultural level and understanding for the clinical trial.
  • •Signed informed consent

排除标准

  • •Subjects with BMI ≥30 or <25 kg /m2
  • •Subjects diagnosed with Diabetes Mellitus.
  • •Subjects with dyslipidemia on pharmacological treatment
  • •Subjects with hypertension on pharmacological treatment
  • •Subjects with established diagnosis of eating disorder
  • •Smokers or those subjects with high alcohol consumption (> 2-3 servings/ day in men and> 1 serving/day in women (1 serving = 1 glass of wine or 1 bottle of beer)
  • •Subjects under pharmacological treatment (except oral contraceptives)
  • •Subjects with large weight fluctuations of more than 4 kg or who have undergone in six months a weight loss diet
  • •Subjects with sensory problems
  • •Subjects with gastrointestinal diseases that affect the digestion or absorption of nutrients
  • •Pregnant or breastfeeding women
  • •Women with menstrual irregularities (absence of menstrual cycle at least 2 months)
  • •Subjects with intense physical activity.
  • •Subjects with food allergies to meals included in breakfast, study product or lunch or that reject their consumption
  • •Subjects with a diagnosis of celiac disease or a gluten intolerance

研究组 & 干预措施

Control Yogurt

Placebo Comparator

Control yogurt

干预措施: Control Yogurt (Other)

Yogurt Variety 1

Experimental

Experimental Yogurt 1: Dextrin, wheat bran, whole oatmeal

干预措施: Yogurt Variety 1 (Other)

Yogurt Variety 2

Experimental

Experimental Yogurt 2: Pea protein, oatmeal

干预措施: Yogurt Variety 2 (Other)

结局指标

主要结局

Change from Baseline Satiety Hunger Assessment

时间窗: Day 1, 8, 15

Visual Analogue Scale (VAS). 100mm horizontal line anchored at each end with the extremes of the subjective feeling to be quantified. Subjects are instructed to rate the sensation being experienced according to how they define the line. e.g., "not at all hungry" (0mm) and "as hungry as I have ever felt" (100mm). Multiple measures are taken at repeated time intervals described below.

次要结局

  • Total amount of food consumed in 24h(Day 1, 8, 15)
  • Change from Baseline Glucose Metabolism Parameters(Day 1, 8, 15)
  • Change from Baseline Lipid Metabolism Parameters(Day 1, 8, 15)
  • Sensory Perception Test(Day 1, 8, 15)
  • Change from Baseline Blood Hormonal Satiety Markers(Day 1, 8, 15)
  • Anthropometric Parameters(Day 1, 8, 15)
  • Amount of food consumed in a "food ad libitum"(Day 1, 8, 15)
  • Adverse Effects(Day 1, 8, 15)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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