Evaluation of the Effectiveness of Standard and Innovative Products That Represent a Substitute Meal for Weight Management in a Reduction Diet
Overweight and Obesity, Body Weight
About this trial
This is an interventional treatment trial for Overweight and Obesity focused on measuring nutrition, overweight, obesity, diet
Eligibility Criteria
Inclusion Criteria: adults aged 18-60 both sexes BMI >27 kg/m2 signed informed consent Exclusion Criteria: significant comorbidities: uncontrolled diabetes mellitus requiring insulin therapy and other endocrine disorders, cardiovascular disorders and other chronic diseases (including malignancies), chronic inflammatory diseases of the gastrointestinal tract, mental disorder people who are currently on or have recently went through an weight loss program (in the past 3 months) people who in the past 6 months had an unwanted and uncontrolled loss of body weight >5% people who underwent bariatric surgery in the past 6 months. people using drugs that increase or decrease appetite permanent therapy with steroid drugs, antidepressants, cytostatics, hormone therapy, beta blockers, etc. people with eating disorders (bulimia) alcohol and drug addicts pregnancy, breastfeeding unstable thyroid disease
Sites / Locations
- Children's Hospital SrebrnjakRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
No Intervention
Active group
Active control
Control group
Participants use the innovative line of products intended for body weight reduction, that represent a meal replacement for weight management
Participants use the standard line of products intended for weight reduction that represent a meal replacement for weight management with already proven clinical effectiveness (positive control).
Participants receive personalized advice on proper nutrition for a reduction diet in which they use common food.