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Acute Effects of Different Macronutrient Compositions and Meal Distributions of the Food

Diet-induced Thermogenesis 2

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02622490
Acronym
DIT2
Enrollment
28
Registered
2015-12-04
Start date
2015-09-30
Completion date
2020-05-31
Last updated
2019-04-24

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

Conditions

Metabolic Rate, Plasma Glucose, Sense of Satiety, Serum Insulin, Serum Triglycerides

Brief summary

About thirty participants, of varying degrees of obesity or being non-obese, without serious concomitant diseases consume either a high- or a low- carbohydrate beverage. The beverage is also consumed either as one single drink or as 5 small portions in the morning and are tested for effects on major cardiovascular risk markers and on metabolic rate for three hours on each occasion.

Detailed description

Thirty participants come to the metabolic ward at about 8 o´clock in the fasting state and stay until lunch on four occasions each. The participants are randomized to the order of the test meals. The meals have a total caloric content of 750 kcal and have either 50% of energy from carbohydrates (low fat) or 20% of energy from carbohydrates (low carb.). The meals are consumed on one occasion in the morning or divided in 5 portions (150 kcal each) for every 30 minutes, i.e. total combinations of meal composition and of meal distribution is 4. Effects of the food on p-glucose, s-insulin, blood-lipids, hormones and on metabolic rate is measured by blood tests or by indirect calorimetry (for metabolic rate). Sense of satiety is measured by visual analogue scales.

Interventions

OTHERtwo test meals with two different macronutrient compositions

Either a high or a low carb meal either as one large or as 5 small meals. ie a crossover trial with one arm

Sponsors

University Hospital, Linkoeping
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Healthy participants \> 18 years with or without obesity

Exclusion criteria

* Major illnesses, * thyroid diseases, * need to take prednisolone, * psychiatric disease, * inability to understand Swedish

Design outcomes

Primary

MeasureTime frameDescription
Metabolic rateDuring about 3 hoursThe metabolic rate is measured before (baseline) and there after repeatedly during 3 hours

Secondary

MeasureTime frameDescription
Effects on glucose and insulin3 hoursRepeated test of glucose and insulin for three hours after test meal

Countries

Sweden

Outcome results

None listed

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