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New treatment option for Obesity
Official title Hormonal Control of Energy and Macronutrient Intake in Obesity (MEMORY)
ClinicalTrials.gov ID: NCT06752967
What this study is testing
- What it's testing
- The overall aim of the MEMORY study is to examine the concept of 'food memory' - how specific macronutrient compositions influence subsequent food preference and intake, and whether this differs across the BMI range from normal weight to obesity.
- 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 45. Healthy volunteers may be eligible.
You may be able to join if
- Age 18-45 years
- For women: Regular menstruation
- BMI-range 18.5-39.9 kg/m\^2
You likely can't join if
- Not able or willing to eat or drink the test meals because of e.g., allergy or intolerance
- Daily smoking
- For women: Pregnancy / planned pregnancy (within the study period) / lactating
- Self-reported history of an eating disorder
- Self-reported weight change (kg) within two months prior to inclusion
- HbA1c ≥48 mmol/mol
See the full eligibility criteria
- Age 18-45 years
- For women: Regular menstruation
- BMI-range 18.5-39.9 kg/m\^2
- Not able or willing to eat or drink the test meals because of e.g., allergy or intolerance
- Daily smoking
- For women: Pregnancy / planned pregnancy (within the study period) / lactating
- Self-reported history of an eating disorder
- Self-reported weight change (kg) within two months prior to inclusion
- HbA1c ≥48 mmol/mol
- Treatment with antidepressants
- Alcohol/drug abuse or in treatment with disulfiram (antabus) at time of inclusion
- Uncontrolled medical issues including but not limited to cardiovascular pulmonary, rheumatologic, hematologic, oncologic, infectious, gastrointestinal, or psychiatric disease; diabetes or other endocrine disease...
- Current treatment with medication which significantly affect appetite or energy balance (e.g., GLP-1 receptor agonists)
- Bariatric surgery
- Unable to understand the informed consent and the study procedures
- Concomitant participation in intervention studies
- Participant's withdrawal of the informed consent
- Other safety concerns - judged by the investigator
The study team makes the final eligibility decision.
Where it's taking place
- Herlev, Denmark, Denmark
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 45 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Herlev, Denmark, Denmark. 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.