Decision-making and Food Intake (Buffet)

August 18, 2025 updated by: Prof. Dr. Soyoung Q Park, German Institute of Human Nutrition

Decision-making and Food Intake ("Buffet Study")

The study will investigate how the expectation of food availability impacts the response to food cues, mood, interoceptive awareness, and consumption of food intake in healthy, naturally cycling women.

Study Overview

Detailed Description

In this within-subjects, randomized crossover study, we will probe how perceived meal availability shapes eating behavior, cognition, and metabolic markers in healthy, naturally cycling women. Each woman attends two appointments in the afternoon (starting at 12 pm after an overnight fast): one in which meal timing and duration are fully disclosed ("certain" condition) and one in which that information is intentionally withheld ("uncertain" condition). During each appointment, participants first undergo a set of cognitive and behavioral tests, then are invited to sample ad libitum from a 30-item buffet under the respective certainty or uncertainty instructions. Venous blood is collected at six fixed intervals to measure fluctuations in ghrelin, leptin, insulin, glucose, and cortisol. To capture real-world eating patterns, participants also log all intake in a smartphone food-tracking app for three days leading up to the initial session.

Study Type

Interventional

Enrollment (Estimated)

45

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Brandenburg
      • Nuthetal, Brandenburg, Germany, 14558
        • Recruiting
        • German Institute of Human Nutrition Potsdam-Rehbruecke
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Nulliparous women (age: 18-35 years) with a regular menstrual cycle (25-32 days)
  • Legally competent/Consent to participate
  • Language proficiency in German (native speaker, fluent)
  • Physically and mentally healthy
  • Body mass index (BMI) of 18.5 - 30 kg/m2

Exclusion Criteria:

  • Current or use of hormonal contraceptives in the previous 6 months
  • Current use of hormonal intra-uterine devices (IUDs)
  • Previous or current pregnancy
  • Diagnosed psychological or metabolic disorder
  • Former or current illnesses of:

    1. Brain or mind (including anxiety disorders, depression, eating disorders, personality disorders, alcohol, drugs or drug or non-substance dependence, neurological disorders other than occasional headache, psychiatric or neurological abnomalities)
    2. Heart or blood circulation/cardiovascular disease (myocardial infarction, stroke, hypertension, hypotension, having a pacemaker)
    3. Gastro-intestinal disorders (e.g. colon diseases, irritable bowel syndrome, Crohn's disease)
    4. Endocrine disorders (e.g. thyroid disorders)
    5. Other serious past or present medical conditions (for example, metabolic syndrome, diabetes)
  • Other serious health problems or current severe mental or physical stress.
  • Blood clotting disorder
  • Fear of drawing blood
  • Severe anemia
  • Previously diagnosed hypoglycemia episodes
  • Regular intake of medication (e.g. Antidepressant/anti-anxiety medication)
  • Blood donation within 4 weeks before the study appointment
  • Intake of anticoagulant medications
  • illegal drug consumption
  • smoking or nicotine consumption
  • extreme athletes
  • vegetarians or vegans or any other dietary restrictions due to allergies or intolerances
  • shift workers

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Perceived food uncertainty
Participants remain unaware of both the scheduled time and the length of the next meal.
Experimental: Perceived food certainty
Participants are aware of both the scheduled time and the length of the next meal.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Laboratory food intake
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Food consumed during a laboratory ad libitum buffet task, in which participants are able to order and consume different foods from a menu of their own liking.
On 1st and 2nd visit (after approximately 30 days)
Food-specific inhibitory control
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Food-specific inhibitory control measured by a go/no-go task adapted from Teslovich et al., 2014.
On 1st and 2nd visit (after approximately 30 days)
Risk propensity on a decision-making task
Time Frame: On 1st and 2nd visit (after approximately 30 days)
In this task, participants decide between a risky/gamble or safe option, based on a paradigm by Liu et al., 2021.
On 1st and 2nd visit (after approximately 30 days)
Delay Discounting behavior in a computerized task
Time Frame: On 1st and 2nd visit (after approximately 30 days)
In this task, participants are asked to choose between an immediate and delayed monetary reward, based on a task paradigm by Eisenstein et al., 2015.
On 1st and 2nd visit (after approximately 30 days)
Range adaptation in reinforcement learning
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Range adaptation in the context of a reinforcement learning task is assessed using a paradigm described by Gueguen et al., 2024.
On 1st and 2nd visit (after approximately 30 days)
Behavioral economic paradigm
Time Frame: On 1st and 2nd visit (after approximately 30 days)
In this task, participants manage a shared resource by deciding how much to extract from a common pool over multiple rounds. Based on their individual extraction, participants receive a monetary reward, which is reduced once the group exceeds a predefined extraction limit. Adapted from Lagenbach et al., 2019.
On 1st and 2nd visit (after approximately 30 days)
Heart rate
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Resting-state and task-based heart rate, measured with a three-point electrocardiogram (ECG)
On 1st and 2nd visit (after approximately 30 days)
Heart-rate variability
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Resting-state and task-based heart-rate variability measured with a three-point electrocardiogram (ECG). Respiratory activity will also be recorded using a breathing belt to correct for breathing-related artifacts.
On 1st and 2nd visit (after approximately 30 days)
Electrodermal activity
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Resting-state and task-based skin conductance measured with two electrodermal activity electrodes placed on the fingers of the non-dominant hand.
On 1st and 2nd visit (after approximately 30 days)
Subjective stress levels
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Subjective stress levels are measured on a semi-continous scale from 1 (not at all) to 100 (extremely) repeatedly during each visit to assess stress responses to perceived food availability. Higher scores indicate greater stress.
On 1st and 2nd visit (after approximately 30 days)
Subjective hunger levels
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Subjective hunger levels are measured on a semi-continous scale from 1 (not at all) to 100 (extremely) repeatedly during each visit to assess changes in subjective hunger ratings in response to perceived food availability. Higher scores indicate greater hunger.
On 1st and 2nd visit (after approximately 30 days)
Subjective fullness levels
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Subjective fullness levels are measured on a semi-continous scale from 1 (not at all) to 100 (extremely) repeatedly during each visit to assess changes in subjective fullness ratings in response to perceived food availability. Higher scores indicate greater fullness.
On 1st and 2nd visit (after approximately 30 days)
Subjective satiety levels
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Subjective satiety levels are measured on a semi-continous scale from 1 (not at all) to 100 (extremely) repeatedly during each visit to assess changes in subjective satiety ratings in response to perceived food availability. Higher scores indicate greater satiation.
On 1st and 2nd visit (after approximately 30 days)
Subjective food cravings
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Subjective cravings for sweet, salty, and fatty foods are measured on a semi-continous scale from 1 (not at all) to 100 (extremely) repeatedly during each visit to assess changes in subjective food craving ratings in response to perceived food availability. Higher scores indicate stronger food craving.
On 1st and 2nd visit (after approximately 30 days)
Levels of diverse hormones
Time Frame: On 1st and 2nd visit (approximately 30 days later)
Levels of different hormones (e.g., estradiol, progesteron, testosterone, ghrelin, leptin) will be measured via blood sampling.
On 1st and 2nd visit (approximately 30 days later)
Levels of cortisol
Time Frame: On 1st and 2nd visit (approximately 30 day later)
Cortosol levels will be assessed multiple times throughout the visit as an objective measure of stress.
On 1st and 2nd visit (approximately 30 day later)
Insulin levels
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Levels of insulin will be measured multiple times throughout the visit via blood sampling.
On 1st and 2nd visit (after approximately 30 days)
Glucose levels
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Glucose levels will be measured multiple times throughout the visit via blood sampling.
On 1st and 2nd visit (after approximately 30 days)
Stress eating
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Changes in food intake related to stress is assessed with the Salzburg Stress Eating Scale (SSES; Meule et al., 2018). Higher Scores indicate increased food intake in response to stress, while lower scores indicate reduced food intake when experiencing stress.
On 1st and 2nd visit (after approximately 30 days)
Reward-related behavioral activation and inhibition
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Reward-related behavioral activation and inhibition are assessed using the Behavioral Inhibition System/Behavioral Activation System questionnaire (BIS/BAS; Strobel et al., 2001). Participants respond on a four-point Likert scale: "strongly disagree," "disagree," "agree," and "strongly agree." Higher scores on the BIS scale indicate greater behavioral inhibition, while higher scores on the BAS scale reflect stronger behavioral activation.
On 1st and 2nd visit (after approximately 30 days)
Impulsivity
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Impulsivity is assessed using the Barratt Impulsiveness Scale (BIS; Meule et al., 2011). Participants respond using a four-point scale: "rarely," "occasionally," "often," and "almost always." Higher scores indicate greater impulsivity.
On 1st and 2nd visit (after approximately 30 days)
Mood
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Mood is measured twice during each visit before and after the ad libitum meal using the Positive and Negative Affect Schedule (PANAS; Janke & Glöckner-Rist, 2014). Participants respond to 20 mood adjectives-10 reflecting positive affect and 10 reflecting negative affect-using a five-point scale: "not at all," "very slightly," "moderately," "quite a bit," and "extremely." Higher scores on the positive affect scale indicate stronger positive mood, while higher scores on the negative affect scale indicate stronger negative mood.
On 1st and 2nd visit (after approximately 30 days)
Emotion regulation
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Emotion regulation is assessed using the Emotion Regulation Questionnaire (ERQ; Abler & Kessler, 2009), which captures individual differences in the use of two distinct strategies to regulate emotions (cognitive reappraisal and expressive suppression). Participants rate their agreement with each item on a seven-point Likert scale, ranging from "strongly disagree" to "strongly agree." Higher scores on each subscale indicate more frequent use of the corresponding regulation strategy.
On 1st and 2nd visit (after approximately 30 days)
Perceived stress
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Perceived stress is assessed using the Perceived Stress Scale (PSS-10; Schneider et al., 2020), which aptures the extent to which individuals perceive their lives as unpredictable, uncontrollable, and overwhelming over the past month. Participants respond to general statements using a five-point scale ranging from "never" to "very often." Higher scores indicate greater perceived stress.
On 1st and 2nd visit (after approximately 30 days)
State anxiety
Time Frame: On 1st and 2nd visit (after approximately 30 days)
State anxiety is assessed twice during each visit before and after the ad lib meal using the state version of the State-Trait Anxiety Inventory (STAI; Grimm, 2009); which captures the current intensity of anxiety as experienced at the moment of assessment. Response options include "almost never". "a little", "moderately", and "very much". Higher scores indicate higher levels of state anxiety.
On 1st and 2nd visit (after approximately 30 days)
Interoceptive awareness
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Interoceptive awareness is assessed using the Multidimensional Assessment of Interoceptive Awareness (MAIA; Eggart et al., 2021). The questionnaire measures various aspects of the awareness of internal bodily sensations. Participants respond to statements using a six-point scale: "never," "very rarely," "rarely," "occasionally," "frequently," and "always." Higher scores reflect greater awareness of bodily sensations.
On 1st and 2nd visit (after approximately 30 days)
Loss of control over eating
Time Frame: on 1st and 2nd visit (after approximately 30 days)
Participants will rate their subjective loss of control over eating during the ad lib buffet task. Higher values indicate greater loss of control.
on 1st and 2nd visit (after approximately 30 days)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Habitual food intake
Time Frame: On three days before the 1st visit
Self-reported habitual food intake (i.e., all food and drinks consumed) is assessed via an app and/or through additional handwritten food diaries on three consecutive days.
On three days before the 1st visit
Quantification of epigenetic markers related to appetite, menstrual cycle, and stress
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Epigenetic markers associated with appetite regulation, menstrual function, and stress response will be measured in blood samples. Site-specific epigenetic modifications (e.g., DNA methylation or histone modifications) will be quantified using validated molecular assays.
On 1st and 2nd visit (after approximately 30 days)
Depressive mood
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Depressive mood is assessed using the German version of the Beck Depression Inventory (BDI; Kühner et al., 2007). The questionnaire measures the severity of depressive symptoms experienced over the past two weeks. Higher total scores indicate more pronounced depressive symptomatology.
On 1st and 2nd visit (after approximately 30 days)
Body image
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Body image is assessed using the Body Shape Questionnaire (BSQ; Pook et al., 2008), which measures concerns related to body shape commonly associated with eating disorders. Participants rate how frequently they experience body-related thoughts and feelings. Higher scores indicate greater body shape concern.
On 1st and 2nd visit (after approximately 30 days)
Trait food cravings
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Food cravings are measured using the trait version of the Food Cravings Questionnaire (FCQ-T; Meule et al., 2012). Responses are given on a six-point scale from "never/not applicable" to "always," with higher scores indicating more frequent and intense cravings.
On 1st and 2nd visit (after approximately 30 days)
Dietary patterns
Time Frame: Day 2 (after approximately 30 days after day 1 i.e., 1st visit)
Dietary patterns are assessed using a food frequency questionnaire (Haftenberger et al., 2018), which captures the frequency and quantity of consumption across various foods and food groups over the past month. Participants indicate how often they consumed specific items and in which quantity, allowing for an overview of habitual dietary intake and eating patterns.
Day 2 (after approximately 30 days after day 1 i.e., 1st visit)
Intuitive eating
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Intuitive eating is assessed using the Intuitive Eating Scale-2 (van Dyck et al., 2019), which evaluates individuals' tendency to rely on physical hunger and satiety cues to guide decisions about when, what, and how much to eat. Participants respond on a five-point scale ranging from "strongly disagree" to "strongly agree." Higher scores reflect a greater inclination toward intuitive eating behaviors.
On 1st and 2nd visit (after approximately 30 days)
Food insecurity status
Time Frame: On 1st and 2nd visit (after approximately 30 days)
Food insecurity status is assessed using the Food Insecurity Experience Scale (FIES; Depa et al., 2018), which evaluates individuals' access to food by addressing factors such as financial constraints, availability, and dietary quality. Response options include "yes," "no," "refused," and "don't know." Higher scores reflect greater severity of food insecurity.
On 1st and 2nd visit (after approximately 30 days)
Restrained eating
Time Frame: Day 1 (1st visit out of 2)
Restrained eating is assessed using the "Cognitive Restraint of Eating" subscale from the Three-Factor Eating Questionnaire (TFEQ; Pudel & Westenhöfer, 1989). The subscale includes both true/false items and statements rated on a four-point Likert scale ranging from 1 ("always") to 4 ("never"). Higher total scores indicate greater cognitive restraint in eating behavior.
Day 1 (1st visit out of 2)
Eating motives
Time Frame: Day 1 (1st visit out of 2)
Eating motives will be assessed using the Eating Motives Survey (TEMS; Renner et al., 2012). Items are rated on a 7-point Likert scale, ranging from "never" to "always". Higher scores on TEMS subscales indicate a greater reliance on those eating motives when making food or eating choices.
Day 1 (1st visit out of 2)
Family climate
Time Frame: Day 1 (1st visit out of 2)
Family climate is measured using the Familien Klima Skale (FKS; Roth, 2003). Items are rated on a 5-point Likert scale ranging from 1) "does not apply at all," 2) "applies little," 3) "applies moderately," 4) "applies predominantly," to 5) "applies almost completely." Higher total scores indicate a better family climate.
Day 1 (1st visit out of 2)
Attachment styles
Time Frame: Day 1 (1st visit out of 2)
Attachment styles will be assessed using the Adult Attachment Scale (AAS; Schmidt et al., 2004). Items are rated on a five-point Likert scale ranging from "not at all true" to "exactly true." Higher scores on each subscale indicate a stronger endorsement of the corresponding attachment dimension. The subscales/attachment styles assessed are secure, avidant, anxious.
Day 1 (1st visit out of 2)
Gut Microbiome
Time Frame: 1 to three days before the 1st visit
To assess the relationship between the gut microbiome and participants' food intake during the ad libitum meal, fecal samples will be collected prior to the first visit, during the observational phase in which participants record their habitual dietary intake.
1 to three days before the 1st visit

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Soyoung Q Park, Prof. Dr., German Institute of Human Nutrition Potsdam-Rehbruecke

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 4, 2025

Primary Completion (Estimated)

July 31, 2026

Study Completion (Estimated)

July 31, 2026

Study Registration Dates

First Submitted

July 29, 2025

First Submitted That Met QC Criteria

August 18, 2025

First Posted (Actual)

August 21, 2025

Study Record Updates

Last Update Posted (Actual)

August 21, 2025

Last Update Submitted That Met QC Criteria

August 18, 2025

Last Verified

August 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • Buffet

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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