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Effect of Meal Composition on the Responses to Meal Ingestion

Factors That Determine the Responses to Meal Ingestion: Meal Composition

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03084276
Enrollment
12
Registered
2017-03-20
Start date
2017-01-16
Completion date
2017-03-21
Last updated
2017-04-25

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

Conditions

Healthy

Keywords

meal ingestion, meal composition, postprandial responses, hedonic sensations, homeostatic sensations, new composition

Brief summary

Aim: to determine to what extent meal composition influences postprandial sensations independently of palatability. The postprandial responses to a low-fat (240 Kcal) versus a high-fat (275 Kcal) test meal (150 g humus) with the same physical and organoleptic characteristics (taste, smell, colour, texture, consistency, temperature) will be studied on a cross-over design. The responses to the meals will be tested on 2 different days. Participants (12 non-obese healthy men) will be instructed to eat a standard dinner the day before, to consume a standard breakfast at home after overnight fast, and to report to the laboratory, where the test meal will be administered 3 h after breakfast. Studies will be conducted in a quiet, isolated room with participants sitting on a chair. Perception will be measured at 5 min intervals 10 min before and 20 min after ingestion and at 10 min intervals up to 60 min after the probe meal.

Interventions

High-fat meal

Low-fat meal with the same physical and organoleptic characteristics as the high-calorie meal.

Sponsors

Hospital Universitari Vall d'Hebron Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* non-obese

Exclusion criteria

* history of gastrointestinal symptoms * prior obesity * use of medications * history of anosmia and ageusia * current dieting * alcohol abuse * psychological disorders * eating disorders

Design outcomes

Primary

MeasureTime frameDescription
Change in digestive well-being measured after the test meal1 dayChange in average well-being measured by 10 score scales at the end of the test meal.

Secondary

MeasureTime frameDescription
Change in satiety measured after the test meal1 dayChange in average satiety measured by 10 score scales at the end of the test meal
Change in fullness sensation measured after the test meal1 dayChange in average fullness measured by 10 score scales at the end of the test meal
Change in abdominal discomfort/pain sensation measured after the test meal1 dayChange in average abdominal discomfort/pain measured by 10 score scales at the end of the test meal
Change in mood measured after the test meal1 dayChange in average mood measured by 10 score scales at the end of the test meal.

Other

MeasureTime frameDescription
Meal palatability1 dayMeal palatability measured by 10 score scales at the end of the test meal.

Countries

Spain

Outcome results

None listed

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