Actively Recruiting
Hormonal Control of Energy and Macronutrient Intake in Obesity (MEMORY)
Led by Steno Diabetes Center Copenhagen · Updated on 2026-04-24
45
Participants Needed
1
Research Sites
80 weeks
Total Duration
On this page
Sponsors
S
Steno Diabetes Center Copenhagen
Lead Sponsor
N
Novo Nordisk A/S
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Hormonal Control of Energy and Macronutrient Intake in Obesity (MEMORY)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 45 years
- Women must have regular menstruation
- Body mass index (BMI) between 18.5 and 39.9 kg/m²
You will not qualify if you...
- Allergies or intolerances preventing consumption of the test meals
- Daily smoking
- Pregnancy, planned pregnancy during the study, or breastfeeding for women
- History of an eating disorder
- Weight change within two months before the study
- HbA1c level equal to or above 48 mmol/mol
- Use of antidepressant medications
- Alcohol or drug abuse or treatment with disulfiram at inclusion
- Uncontrolled medical conditions including cardiovascular, pulmonary, rheumatologic, hematologic, oncologic, infectious, gastrointestinal, psychiatric, diabetes, endocrine diseases, or immunosuppression
- Current use of medications affecting appetite or energy balance
- Previous bariatric surgery
- Inability to understand consent or study procedures
- Participation in other intervention studies
- Withdrawal of consent
- Other safety concerns as judged by the investigator
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Steno Diabetes Center Copenhagen
Herlev, Denmark, Denmark, 2730
Actively Recruiting
Research Team
J
Jonas S. Quist, MSc, PhD
CONTACT
T
Trine Spragge Ekblond, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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