Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
100 participants
INTERVENTIONAL
2025-09-29
2025-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
FACTORIAL
PREVENTION
SINGLE
Study Groups
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LL
Meal low in energy density, low in ultra-processed food
Meal low in energy density, low in ultra-processed food
Meal low in energy density, low in ultra-processed food
LH
Meal low in energy density, high in ultra-processed food
Meal low in energy density, high in ultra-processed food
Meal low in energy density, high in ultra-processed food
HL
Meal high in energy density, low in ultra-processed food
Meal high in energy density, low in ultra-processed food
Meal high in energy density, low in ultra-processed food
HH
Meal high in energy density, high in ultra-processed food
Meal high in energy density, high in ultra-processed food
Meal high in energy density, high in ultra-processed food
Interventions
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Meal low in energy density, low in ultra-processed food
Meal low in energy density, low in ultra-processed food
Meal low in energy density, high in ultra-processed food
Meal low in energy density, high in ultra-processed food
Meal high in energy density, low in ultra-processed food
Meal high in energy density, low in ultra-processed food
Meal high in energy density, high in ultra-processed food
Meal high in energy density, high in ultra-processed food
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Body mass index (BMI) 18.5-35.0 kg/m2
* Weight stability the last 3 months +/-5%
Exclusion Criteria
* 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
18 Years
64 Years
ALL
Yes
Sponsors
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Göteborg University
OTHER
Responsible Party
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Principal Investigators
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Linnea Bärebring, PhD, Associate professor
Role: PRINCIPAL_INVESTIGATOR
Göteborg University
Locations
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University of Gothenburg
Gothenburg, , Sweden
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2025-02415-01
Identifier Type: -
Identifier Source: org_study_id
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