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Effects of Low Calorie Sweeteners on Dietary Intakes, Hunger, Appetite and Satiety

Effects of Beverages Containing Low Calorie Sweeteners (LCS) on Energy and Macronutrient Intakes and on Hunger, Appetite and Satiety Sensations

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02297880
Enrollment
170
Registered
2014-11-21
Start date
2014-10-31
Completion date
2016-03-31
Last updated
2017-02-09

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

Conditions

Eating Behavior

Keywords

low calorie sweetener satiety, intake, hunger

Brief summary

Although there is evidence that low calorie sweeteners (LCS) do not stimulate hunger or appetite, divergent opinions appear regularly both in the scientific literature and in the popular press. The goal of this study is to examine the effects of LCS containing beverages on appetite and intake in healthy individuals.

Detailed description

The study will be a monocentric randomized controlled open trial including two parallel groups to examine effects of LCS beverages as compared to water on daily intakes of energy and macronutrients. The effects of LCS beverages on hunger, satiety, desire to eat and on the selection of sweet or savory foods eating occasions will be assessed.

Interventions

OTHERBeverage containing low calorie sweeteners

Beverage containing low calorie sweeteners

Still water (no flavour)

Sponsors

CreaBIO
CollaboratorUNKNOWN
The Coca-Cola Company
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Body Mass Index: Lower limit 18 kg/m²; Upper limit 28 kg/m²; weight stable within ± 3 kg in the last 6 months * Habitual energy intake within the 95% confident interval of the reference energy intake for the French population (as provided by the INCA 2 survey * Must not be a regular drinker of LCS beverages (less than once a week no more than every 15 days) and be willing to use LCS according to protocol * For female participants: not pregnant, not breast feeding, planning to become pregnant during the study or on contraception since at least 3 months (regular 28-day cycle) * Subject registered with the French Social Security.

Exclusion criteria

* Currently diagnosed somatic pathology * On medication affecting metabolism, weight, energy intake, or energy expenditure in the last 6 months * Major psychiatric disorder, particularly eating disorders as defined by the Diagnostic and Statistical Manual od Mental Disorders-IV * Rejection of sweet foods or drinks as revealed by the diet history * Smoking subject planning to stop smoking in the next 3 months * Subjects suffering from food allergies or intolerance * Subject not capable of understanding the constraints of the study and who not agree to abide

Design outcomes

Primary

MeasureTime frameDescription
Subjective sensations: hunger, satiety and desire to eat9 weeksVisual Analog Scales

Secondary

MeasureTime frameDescription
Energy and macronutrient intakes9 weeksDiet history questionnaire
Anthropometric parameters9 weeksbody weight, height, waist and hip circumferences

Countries

France

Outcome results

None listed

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