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NCT Number: NCT07133529

Decision-making and Food Intake

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.

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

German Institute of Human Nutrition Potsdam-Rehbruecke

Nuthetal, Brandenburg, 14558, Germany

Location status: Recruiting

Location contact

Recruitment officer

CONTACT

[email protected]

+4933200882752

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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:
  • 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)
  • Heart or blood circulation/cardiovascular disease (myocardial infarction, stroke, hypertension, hypotension, having a pacemaker)
  • Gastro-intestinal disorders (e.g. colon diseases, irritable bowel syndrome, Crohn's disease)
  • Endocrine disorders (e.g. thyroid disorders)
  • 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

Treatment and study plan

Perceived food uncertainty

Behavioral

Participants remain unaware of both the scheduled time and the length of the next meal.

Perceived food certainty

Behavioral

Participants are aware of both the scheduled time and the length of the next meal.

Primary outcomes

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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)

  8. 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.

  9. 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.

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  15. 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.

  16. 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.

  17. 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.

  18. 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.

  19. 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.

  20. 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.

  21. 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.

  22. 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.

  23. 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.

  24. 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.

  25. 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.

  26. 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.

  27. 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.

Secondary outcomes

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. 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.

  12. 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.

  13. 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Elisa Rehbein, Dr.

CONTACT

[email protected]

+49 33 200 88 - 2525

Renée Sophie Cuntz, MSc

CONTACT

[email protected]

+49 33 200 88 2519

Sponsors and collaborators

Lead sponsor

German Institute of Human Nutrition

Other

Registry information

Official study title

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

Acronym: Buffet

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Aug 21, 2025
Registry last updated
Aug 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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