Influence of two formula diets on satiety, attention and concentratio
- Conditions
- Satiety, attention and concentration
- Registration Number
- DRKS00009913
- Lead Sponsor
- eibniz Universität Hannover, Institut für Lebensmittelwissenschaft und Humanernährung, Abteilung Ernährungsphysiologie und Humanernährung
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
BMI: 18,0 - 28,0 kg/m2
- Age: 18-50years
- Men and Women
- Written consent after information about study contents and study procedure
- Ability and willingness of study participants to follow study leaders instructions
- severe chronic illness (manifest coronary heart disease, cancer)
- severe kidney or liver diseases
- insulin-dependent diabetes mellitus Typ I and II
- continuous intake of corticosteroids (not inhalation), psychotropic drug
- chronic gastroinestinal diseases (especially small intestine e.g. duodenal ulcer, liver, pancreas)
- known endokrine and immunological diseases
- Hormonal disorders, for example, hyperthyroidism and Cushing's syndrome
- Treatment with non-insulin-releasing antidiabetics (guar, acarbose)
-existing intolerances or allergies to ingredients of the diet
- lactose or fructose malabsorption
- intolerance towards soy and milk protein
- continuous intake of laxatives
- pregnancy
- lactation
- addiction to alcohol and/or drugs
- immediate planned surgery
- simultaneous participation at another clinical trial or participation within the last 30 days
- missing consent or refusing / reset of the consent
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method attention and concentration measured by colour/word interfernce test (Stroop) 30 and 90 minutes after formula diet intake
- Secondary Outcome Measures
Name Time Method satiety shall be measured via visual analogue scale before and 15, 30, 45, 60, 90 and 120 min after formula diet intake