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New treatment option for Appetite
Official title Metabolic Effects of Short-term Ultra-processed Food Intake (MEST-UPF)
ClinicalTrials.gov ID: NCT07213245
What this study is testing
- What it's testing
- The overall aim of this project is to study the effects of short-term high ultra-processed food intake, compared to nutrient- and energy density matched low ultra-processed food (UPF) intake, on energy intake and appetite. A total of 24 men and women who meet all inclusion criteria and none of the exclusion criteria will be invited to participate.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 50. Healthy volunteers may be eligible.
You may be able to join if
- Body mass index (BMI) 18.5-30 kg/m2
- Fasting glucose \< 6.1 mmol/l
- Hb \>110 g/L
- Weight stability the last 3 months +/-5%
You likely can't join 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...
- Pregnant, lactating or planning a pregnancy during the study period.
- Blood donation or participation in a clinical study with blood sampling within 30 days prior to screening visit and throughout the study.
- History of gastrointestinal conditions or major gastrointestinal surgery (Inflammatory bowel disease, Crohn's disease, malabsorption, colostomy...
- Type 1 diabetes or type 2 diabetes.
See the full eligibility criteria
- Body mass index (BMI) 18.5-30 kg/m2
- Fasting glucose \< 6.1 mmol/l
- Hb \>110 g/L
- Weight stability the last 3 months +/-5%
- 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.
- Blood donation or participation in a clinical study with blood sampling within 30 days prior to screening visit and throughout the study.
- History of 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.
- Thyroid disorder.
- Current smoking, vaping.
- Following any weight reduction program or having followed one during the last 6 months prior to screening.
- Not habitually eating breakfast (\<5 times/week).
- Restrained eating based on the three-factor eating questionnaire.
The study team makes the final eligibility decision.
Where it's taking place
- Gothenburg, Sweden
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 50 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Gothenburg, Sweden. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.