NCT07178405

Brief Summary

The overall aim of the study is to determine effects of different meal characteristics on energy intake, eating rate and appetite.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
85

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 26, 2025

Completed
22 days until next milestone

First Posted

Study publicly available on registry

September 17, 2025

Completed
12 days until next milestone

Study Start

First participant enrolled

September 29, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 27, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 27, 2025

Completed
Last Updated

February 4, 2026

Status Verified

January 1, 2026

Enrollment Period

2 months

First QC Date

August 26, 2025

Last Update Submit

February 2, 2026

Conditions

Keywords

AppetiteDietInterventionSingle meal study

Outcome Measures

Primary Outcomes (2)

  • Energy intake

    Energy intake estimated by nutrient calculation of leftover food

    Baseline until 1 hour, or completion of the meal (which ever comes first)

  • Eating rate

    Time it takes to eat the study meal until satisfied

    Baseline until 1 hour, or completion of the meal (which ever comes first)

Secondary Outcomes (2)

  • Self-reported appetite

    Before, and after the meal (before meal and after 30 minutes, 1hour, 1.5 hours, 2 hours and 4 hours)

  • Self-reported prospective energy intake

    From 30 min until midnight or bedtime (which ever comes first)

Study Arms (4)

LL

EXPERIMENTAL

Meal low in energy density, low in ultra-processed food

Other: Meal low in energy density, low in ultra-processed food

LH

EXPERIMENTAL

Meal low in energy density, high in ultra-processed food

Other: Meal low in energy density, high in ultra-processed food

HL

EXPERIMENTAL

Meal high in energy density, low in ultra-processed food

Other: Meal high in energy density, low in ultra-processed food

HH

EXPERIMENTAL

Meal high in energy density, high in ultra-processed food

Other: Meal high in energy density, high in ultra-processed food

Interventions

Meal low in energy density, high in ultra-processed food

Also known as: LH
LH

Meal high in energy density, low in ultra-processed food

Also known as: HL
HL

Meal high in energy density, high in ultra-processed food

Also known as: HH
HH

Meal low in energy density, low in ultra-processed food

Also known as: LL
LL

Eligibility Criteria

Age18 Years - 64 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Age 18-64 years
  • Body mass index (BMI) 18.5-35.0 kg/m2
  • Weight stability the last 3 months +/-5%

You may not qualify if:

  • Food allergies, intolerances or preferences preventing consumption of any products included in the study.
  • Unable to sufficiently understand written and spoken Swedish or English to provide written consent and understand information and instructions from the study personal.
  • Pregnant, lactating or planning a pregnancy during the study period.
  • History of stomach or gastrointestinal conditions or major gastrointestinal surgery (Inflammatory bowel disease, Crohn's disease, malabsorption, colostomy, bowel resection, gastric bypass surgery etc.)
  • Type 1 diabetes or type 2 diabetes.
  • Drug treated thyroid disorder
  • - Following any weight reduction program or having followed one during the last 6 months prior to screening.
  • Medication for weight reduction purpose effecting appetite or fat absorption (e.g. GLP-1 analogues, orlistat)
  • Severe dysfunctional eating behavior based on Three Factor Eating Questionnaire

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Gothenburg

Gothenburg, 40530, Sweden

Location

MeSH Terms

Conditions

Obesity

Interventions

Food, Processed

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

FoodDiet, Food, and NutritionPhysiological PhenomenaFood and Beverages

Study Officials

  • Linnea Bärebring, PhD, Associate professor

    Göteborg University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
FACTORIAL
Model Details: 2\*2 factorial
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 26, 2025

First Posted

September 17, 2025

Study Start

September 29, 2025

Primary Completion

November 27, 2025

Study Completion

November 27, 2025

Last Updated

February 4, 2026

Record last verified: 2026-01

Locations