Hormonal Control of Energy and Macronutrient Intake in Obesity (MEMORY)
Recruiting now · Not applicable
Conditions studied: Obesity, Normal Weight, Overweight
In brief
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.
Key facts
- Study ID
- NCT06752967
- Run by
- Steno Diabetes Center Copenhagen
- People needed
- 45
- Starts
- 2024-12-12
- Expected to finish
- 2026-06-29
- Last updated by the study team
- 2026-04-24
Who can join
Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 18-45 years
- For women: Regular menstruation
- BMI-range 18.5-39.9 kg/m\^2
You may not qualify 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
- 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; immunosuppression
- 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
Where it is running
- Steno Diabetes Center Copenhagen — Herlev, Denmark, Denmark (enrolling)
Full record on ClinicalTrials.gov
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