Fact CheckerSign in

NCT06992921Completed

Towards Personalized Nutrition With SCAPIS2-HOME

Towards Personalized Nutrition With SCAPIS2-HOME - Dissecting Determinants of Interpersonal Metabolic Responses to Standardized Meals and Mixed Meal Tolerance Tests

Source: ClinicalTrials.gov · Last updated 19 Mar 2026

Brief summary (registry, in English)

The Swedish CardioPulmonary bioImage Study (SCAPIS) is a nationwide, open-access, population-based cohort in Sweden designed to study cardiovascular disease and chronic obstructive pulmonary disease. In January 2024, the reexamination of half of the cohort from SCAPIS1 started (the SCAPIS2). In SCAPIS2-HOME (a sub-study of SCAPIS2), individual responses to standardized isocaloric breakfasts and repeated Mixed Meal Tolerance Tests (MMTTs) will be investigated. For this purpose, participants from the SCAPIS baseline cohort will be invited to take part in a 10-day intervention study, where participants will consume breakfast meals at clinic and the MMTTs at home. The breakfast meals will include ordinary cereal products that consist of either whole grain or refined grain foods served along with other typical breakfast items to be part of either a low-carbohydrate/high-fat or high-carbohydrate/low-fat breakfast. For the MMTTs, we will use standardized meal formulas called PhenFlex, which are high in calories, fat, and glucose and will be consumed repeatedly at home in the evening or the morning. Blood samples will be analyzed using clinical markers such as C-peptide, triglycerides, and markers of inflammation along with metabolomics. Continuous glucose monitoring will be used to obtain 24-hour interstitial glucose concentrations every 15 minutes during the 10-day intervention. Fecal- and blood samples will also be collected along with dietary assessments. The research aims to understand the differential metabolic responses (glycemia, insulinemia, lipid profile, inflammation markers, and key metabolites) individuals may show after consuming whole grains or refined grains as part of breakfasts with high or low carbohydrate content. It is further to characterize to what extent an individual's specific characteristics, including the microbiota, health status, anthropometry, and habitual diet, drive such response differences. Since the study is a sub-set of the SCAPIS cohort, there are unique possibilities to relate the postprandial responses to hard risk factors such as prediabetic status (measured by oral glucose tolerance test), hepatic steatosis (liver fat deposition) and atherosclerotic plaque in the coronary arteries.

Status (registry)
Completed
Study type
Interventional
Enrollment
1641 (actual)
First submitted
30 Apr 2025
Start date
1 Jan 2024
Primary completion date
27 Nov 2025
Lead sponsor
Chalmers University of Technology
Diseases
COPD
NCT number
NCT06992921

What you commit to

  • Study type: Interventional
  • Participants enrolled: 1641
  • From 1 Jan 2024 to the primary completion date, 27 Nov 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Bariatric surgery, gastric bypass, or sleeve.

Other illness

  • Food allergies or intolerances preventing consumption of any products included in the study

Who the study is looking for

  • \- Participants from the Swedish CArdioPulomonary bioImage Study (SCAPIS)

Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sahlgrenska University Hospital/Östra Hospital
Coordinator of this site? Confirm its status
GothenburgSwedenUnknown status
Region Västerbotten (Kliniskt Forskningscentrum)
Coordinator of this site? Confirm its status
UmeåSwedenUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.