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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06386237
Other study ID # UVienna_NDNL_1
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 8, 2024
Est. completion date February 28, 2025

Study information

Verified date April 2024
Source University of Vienna
Contact Stefan Schulreich, Prof. Dr.
Phone +4314277
Email stefan.schulreich@univie.ac.at
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the present study is to investigate the effects of different meal interventions on cognition (i.e., learning and decision making) and brain activity in healthy participants.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date February 28, 2025
Est. primary completion date February 28, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - 18 to 40 years old - fluent in German - right-handed - able to safely undergo MRI scanning - BMI (Body-Mass-Index) between 18.5 and 29.9 kg/m2 Exclusion Criteria: - current medication that might interfere with the processes studied - any metabolic, gastrointestinal, cardiological, neurological, psychiatric or any recurring or chronic diagnoses - drug use - alcohol consumption > 10 g/d for women and > 20 g/d for men - smoking - shifted circadian rhythm (e.g. jetlag, shift work) - vegan or vegetarian diet - food intolerances - females: hormonal contraception, pregnancy, lactation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Dietary intervention: Standardized breakfast with varying amounts of macronutrients (in particular carbohydrate/protein ratios)
Participants receive a standardized meal with one type of macronutrient composition in one experimental session and the other type in a different experimental session a few days apart (within-subjects crossover design; i.e. order counterbalanced)

Locations

Country Name City State
Austria University of Vienna Vienna

Sponsors (2)

Lead Sponsor Collaborator
University of Vienna Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in cognition/behavior I Changes in learning behavior assessed via computer-based learning task ("predictive inference task") which tracks choices and response times (allows for calculation of learning-related scores: change in prediction choice following feedback) 3-4.5 hours (post-meal)
Primary Changes in cognition/behavior II Changes in decision-making behavior assessed via computer-based decision task ("gamble task") which tracks choices (calculation of gamble acceptance frequencies) and response times. 3-4.5 hours (post-meal)
Primary Changes in brain activity Changes in brain activity measured via functional magnetic resonance imaging; 3-4.5 hours (post-meal)
Secondary Changes in metabolic parameters I Changes in the concentrations of amino acids (assessed via blood samples and chemical analysis) from baseline (prior meal) to approx. 4.5 hours after meal at several time points
Secondary Changes in metabolic parameters II Changes in the concentrations of glucose (assessed via blood samples and chemical analysis) from baseline (prior meal) to approx. 4.5 hours after meal at several time points
Secondary Changes in metabolic parameters III Changes in the concentrations of insulin (assessed via blood samples and chemical analysis) from baseline (prior meal) to approx. 4.5 hours after meal at several time points
Secondary Changes in metabolic parameters IV Changes in the concentration of cortisol (assessed via saliva samples and chemical analysis) from baseline (prior meal) to approx. 4.5 hours after meal at several time points
Secondary Changes in subjective affective state Changes in reported affect ("Multidimensionaler Befindlichkeitsfragebogen" - multidimensional mood scale; Steyer et al., 1997) from baseline (prior meal) to approx. 4.5 hours after meal at several time points
Secondary Changes in experienced hunger Changes in subjective reported hunger (assessed via single-item Likert-Scale) rom baseline (prior meal) to approx. 4.5 hours after meal at several time points
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