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Encapsulated Flavour Effects on Satiety

Pilot Study to Evaluate the Satiating Effect Using Different Gummies With Encapsulated Flavours in a Group of Healthy Overweight Subjects

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03621358
Acronym
SACIGOMA
Enrollment
12
Registered
2018-08-08
Start date
2018-04-13
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, Encapsulated flavour, Gummies, Visual Analogue Scale, Cross-over

Brief summary

The purpose of this study is to evaluate the satiating effects of different gummies with encapsulated flavour on overweight subjects (BMI ≥25 and \<30 kg / m2). Some studies have shown that the contribution of different flavours could reduce food intake. This have made grown the interest of food industry in incorporate these compounds in food and to being able to develop new functional foods into the control of body weight, as well as variables of glucose metabolism and lipid profile, which can contribute to te prevention of cardiovascular diseases.

Detailed description

A randomized, cross-over and double-blind pilot study with 3 study arms is being performed to evaluate the satiating properties of the encapsulated flavours in different gummies 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

OTHERControl gummy with free flavour (without encapsulating)

12 g/day (3 gummies)

OTHERExperimental gummy with 50% free/50% encapsulated flavour

12 g/day (3 gummies)

OTHERExperimental gummy with 100% encapsulated flavour

12 g/day (3 gummies)

Sponsors

Creaciones Aromáticas Industriales S.A.
CollaboratorOTHER
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 PerceptionDay 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