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Enriched Yogurts With Soluble Fibre or Vegetable Protein on Satiety

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03625245
Acronym
SACIYOGU
Enrollment
12
Registered
2018-08-10
Start date
2018-05-10
Completion date
2018-09-30
Last updated
2022-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overweight

Keywords

Satiety, Vegetable protein, Yogurt, Fiber, Visual Analogue Scale, Cross-over

Brief summary

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.

Detailed description

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.

Interventions

125 g/day

OTHERYogurt Variety 1

125 g/day

OTHERYogurt Variety 2

125 g/day

Sponsors

Go Fruselva, S.L.
CollaboratorUNKNOWN
Instituto de Investigación Hospital Universitario La Paz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)

Masking description

Double Blind (Participant and Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Men and women from 18 to 65 years old. * Body Mass Index (BMI) ≥25 and \<30 kg/m2. * Adequate cultural level and understanding for the clinical trial. * Signed informed consent

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Satiety Hunger AssessmentDay 1, 8, 15Visual 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.

Secondary

MeasureTime frameDescription
Amount of food consumed in a food ad libitumDay 1, 8, 15120 min After eating the study product
Total amount of food consumed in 24hDay 1, 8, 1524h Food Record Method
Change from Baseline Glucose Metabolism ParametersDay 1, 8, 15Glucose
Change from Baseline Blood Hormonal Satiety MarkersDay 1, 8, 15GLP1, Peptide YY, Ghrelin, Leptin, GIP, Peptide C
Anthropometric ParametersDay 1, 8, 15Weight and height will be combined to report BMI in kg/m2
Sensory Perception TestDay 1, 8, 15Questionnaire of analysis of sensory perception of the food study product. Five questions that are valued on a scale of 0% to 100% asking about the taste and smell of the study product: desire with which the product is taken, taste, smell, consistency and what wait for effectiveness.
Adverse EffectsDay 1, 8, 15Gastrointestinal Symptoms (Nausea, Diarrhea, Bloating and other disorders)
Change from Baseline Lipid Metabolism ParametersDay 1, 8, 15Cholesterol, LDL-C, HDL-C, TG

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026