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Influence of two formula diets on satiety, attention and concentration

Influence of two formula diets on satiety, attention and concentration

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00009913
Enrollment
20
Registered
2016-02-05
Start date
2016-02-09
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Satiety, attention and concentration

Interventions

Group 1: Within the six week cross over study participants obtain in a random order a protein rich meal replacement for three times with an interval of one week. A protein-rich meal replacement cons

Sponsors

Leibniz Universität Hannover, Institut für Lebensmittelwissenschaft und Humanernährung, Abteilung Ernährungsphysiologie und Humanernährung
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: - 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

Exclusion criteria

Exclusion criteria: - 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

Design outcomes

Primary

MeasureTime frame
attention and concentration measured by colour/word interfernce test (Stroop) 30 and 90 minutes after formula diet intake

Secondary

MeasureTime frame
satiety shall be measured via visual analogue scale before and 15, 30, 45, 60, 90 and 120 min after formula diet intake

Countries

Germany

Contacts

Public ContactKatharina Möller

oLeibniz Universität Hannover, Institut für Lebensmittelwissenschaft und Humanernährung, Abteilung Ernährungsphysiologie und Humanernährung

moeller@nutrition.uni-hannover.de0511-762 3317

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026