The project aims to examine the efficacy of a 12-week intake of alginate based ready to drink supplement on development in body weight and body composition, and risk markers for type-2 diabetes and cardiovascular disease in obese subjects.
The study consists of a parallel RCT with 96 overweight/obese subjects enrolled into two treatment arms: placebo or active for 12 weeks. They will undergo examination at time points 0 and 12 weeks where a DXA scan will be performed to assess body composition and a fasting blood sample will be taken. At time points 0, 2, 4, 6, 8, 10 and 12 weeks their weight and waist circumference and number of test products not consumed will be recorded. In addition all subjects receive dietary counselling during the 12 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
96
The dosage is 3x500ml daily
The dosage is 3x500ml daily
Department of Human Nutrition
Frederiksberg, Copenhagen, Denmark
Body weight
Time frame: 12 Weeks
Blood pressure
Time frame: 12 weeks
Risk markers for type 2 diabetes
Time frame: 12 weeks
Risk markers for cardiovascular disease
Time frame: 12 Weeks
Body composition
Time frame: 12 Weeks
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