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Completed

NCT Number: NCT07257692

Effect of Feeding Status on Appetite and Eating Behaviour.

This clinical trial's primary aim is to evaluate the impact of a short-term feeding state on trait eating behaviours and weekly appetite. The researchers will compare two groups (before vs. after a meal) to see if the meal affects appetite and eating behaviour traits in healthy adults.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

New Lister Building at Glasgow Royal Infirmary

Glasgow, G31 2ER, United Kingdom

About this study

Study Design

Screening visit (Visit 1) Participants will be asked to complete a health screening questionnaire. Only those in generally good health will be enrolled. Following this, weight and height will be measured, and the body mass index (BMI) will be determined. Finally, participants will complete the International Physical Activity Questionnaire and food preferences questionnaire to ensure they like the foods provided in the study. Moreover, they will be provided with a 24-hour food diary to complete 24 hours before the first experimental trial, along with a set of scales to help them measure and record all items. Participants will be instructed to follow this food diary in the 24 hours before the second trial, ensuring that the food and drink consumed in the 24 hours before each experimental trial are similar.

Experimental trials (Visits 2 and 3) In the 24 hours prior to the experimental trial, participants will complete a 24-hour food diary where they record all food and beverages. With this diary, participants will describe all drinks and food consumed using household measures (e.g. teaspoon, cup). They will be asked to record a detailed description of food and/or drink intake, time and place of consumption. They will also record details on food brands, preparation and cooking methods. Portion sizes should be estimated using household measures or natural unit sizes (e.g., slices of bread). Food diaries and an electronic kitchen scale (Salter Housewares Ltd., Tonbridge, UK) will be provided to subjects, and they will be shown how to use the scales and how to record. They will follow this food diary in the 24 hours prior to the second visit to ensure they replicate their food and drink consumption in the 24 hours before each experimental trial.

Participants will arrive at the laboratory before both experimental trials at approximately 08:30, having fasted for at least 12 hours (participants instructed not to eat or drink after 20:30 from the previous night, except water). They will be weighed and then, at approximately 09:30. They will consume a standardised breakfast comprising porridge oats, full-fat milk, croissants, butter, jam and orange juice, which they will have 30 minutes to consume. Participants will then rest in the metabolic research unit for the remaining 3.5 hours of the trial (5-hour visit in total), completing study questionnaires where necessary. They will be able to consume water ad libitum and will be able to bring laptops/tablets and books.

During the experimental trial, participants will complete the weekly Visual Analogue Scale (wVAS), the Three Factor Eating Questionnaire (TFEQ) and the Intuitive Eating Scale-2 (IES-2) in the fasted state before the breakfast meal; while in the second trial, participants will be asked to complete these 90 minutes after the administration of the breakfast meal. In a randomised counter-balanced design, half of the participants will complete these scales in the fasted state first, whilst the other half will complete these scales after the breakfast meal first.

Throughout both experimental trials, participants will be periodically asked to complete measures of instantaneous appetite and food cravings. Instantaneous appetite ratings will be measured through the instantaneous Visual Analogue Scale (iVAS). These will examine various appetite constructs: hunger, satisfaction, fullness, prospective food consumption and desire to eat. Participants will be asked to place a vertical mark on the horizontal line at a point corresponding to their feelings at that time (hence the term instantaneous appetite). Participants will complete iVAS first at approximately 09:00, just before the breakfast meal. Thereafter, iVAS will be administered every 60 minutes (five assessments in total).

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Adults aged 18 years or older.
  • Have stable body mass for at least three months (within ±2 kg).

Exclusion criteria

  • People who are younger than 18 or older than 65 years old.
  • Have food allergies.
  • SmokingTaking medications
  • Suffering from metabolic health issues, e.g., history of diabetes, cardiovascular disease, or eating disorders.

Treatment and study plan

Standardised meal

Dietary Supplement

Participants will complete the wVAS (weekly visual analogue scale), the TFEQ (Three factor eating questionnaires)and the IES-2 (Intuitive eating scale-2)in the fasted state before the breakfast meal.

Primary outcomes

  1. Dietary restraint

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Dietary restraint is the cognitive effort or intention to consciously limit food intake of eating. Participants will complete assessments of the Three Factor Eating Questionnaire (TFEQ) (Stunkard et al., 1985) to assess restraint once at two different time points on each experimental trial in a randomised, counterbalanced fashion. The minimum score for restraint is 0 and the maximum is 20, with a higher score indicating higher levels of restraint.

  2. Disinhibition

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Disinhibition refers to the tendency to overeat in response to emotional, social, or situational cues, even when not physiologically hungry. Participants will complete assessments of the Three Factor Eating Questionnaire (TFEQ) (Stunkard et al., 1985) to assess disinhibition once at two different time points on each experimental trial in a randomised, counterbalanced fashion. The minimum score for disinhibition is 0, and the maximum is 16, with a higher score indicating greater disinhibition or loss of control over eating.

  3. Hunger

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Hunger reflects the subjective perception of appetite and the susceptibility to feelings of hunger and food cues. Participants will complete assessments of the Three Factor Eating Questionnaire (TFEQ) (Stunkard et al., 1985) to assess hunger once at two different time points on each experimental trial in a randomised, counterbalanced fashion. The minimum score for hunger is 0 and the maximum is 14, with a higher score indicating indicating greater susceptibility to feelings of hunger and greater responsiveness to food cues.

  4. Unconditional Permission to Eat (UPE)

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Unconditional Permission to Eat reflects a person's ability to allow themselves to eat a wide range of foods without guilt or unnecessary rules. It captures how flexible and trusting someone is toward their own hunger cues. Participants will complete the Intuitive Eating Scale-2 (IES-2) (Tylka & Kroon Van Diest, 2013) to assess UPE at two time points during each experimental trial in a randomised, counterbalanced order. Items are rated on a 5-point scale from 1 (strongly disagree) to 5 (strongly agree), with higher scores indicating a greater ability to permit oneself to eat when hungry without external restrictions.

  5. Eating for Physical Rather Than Emotional Reasons (EPR)

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Eating for Physical Rather Than Emotional Reasons reflects the extent to which individuals eat in response to genuine physical hunger rather than emotions such as stress, boredom, or sadness. This construct captures a healthy separation between emotional states and eating behaviour. Participants will complete the IES-2 (Tylka & Kroon Van Diest, 2013) at two time points during each experimental visit in a randomised, counterbalanced order. Items are scored on a 1-5 scale, with higher values indicating a stronger tendency to eat based on physical hunger rather than emotional triggers.

  6. Reliance on Hunger and Satiety Cues (RHSC)

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Reliance on Hunger and Satiety Cues measures how effectively individuals listen to and trust their internal bodily signals to guide when, what, and how much to eat. It reflects a mindful and attuned approach to eating. Participants will complete the IES-2 (Tylka & Kroon Van Diest, 2013) at two different time points on each study day in a randomised, counterbalanced fashion. Items are rated on a 5-point scale, and higher scores indicate stronger trust in one's internal cues of hunger and fullness.

  7. Body-Food Choice Congruence (BFCC)

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Body-Food Choice Congruence reflects how consistently individuals choose foods that support their physical functioning, health, and well-being. It captures a compassionate connection between how a person feels and the types of foods they select. Participants will complete the IES-2 (Tylka & Kroon Van Diest, 2013) at two time points during each experimental visit in a randomised, counterbalanced design. Items use a 1-5 response scale, with higher scores indicating greater alignment between food choices and physical self-care.

  8. Hunger

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Hunger represents how frequently and intensely participants felt hungry over the past week. Using the weekly Visual Analogue Scale (wVAS) (Womble et al., 2003), participants rate their overall hunger on a 100-mm line from 0 mm (not hungry at all during the week) to 100 mm (extremely hungry throughout the week). Higher scores indicate stronger or more frequent hunger sensations during the previous week.

  9. Fullness

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Fullness reflects how often or how strongly participants felt full across the previous week. Using the weekly Visual Analogue Scale (wVAS) (Womble et al., 2003), participants will complete the wVAS, marking fullness on a 100-mm scale from 0 mm (rarely or never felt full during the week) to 100 mm (felt very full very often throughout the week). Higher scores indicate more frequent or stronger feelings of fullness across the week.

  10. Satisfaction with eating

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Satisfaction reflects how content or pleased participants felt with their eating experiences during the past week. Using the weekly Visual Analogue Scale (wVAS) (Womble et al., 2003), participants rate satisfaction on a 0-100 mm line from 0 mm (not satisfied at all during the week) to 100 mm (extremely satisfied with eating throughout the week). Higher scores indicate greater overall satisfaction during the week.

  11. Desire to Eat

    Time frame: Once before the breakfast meal and once 90 minutes after the meal during each experimental trial.

    Desire to eat reflects how frequently participants experienced an urge or motivation to eat during the previous week. Using the weekly Visual Analogue Scale (wVAS) (Womble et al., 2003), participants will rate this on the wVAS, from 0 mm (little or no desire to eat during the week) to 100 mm (strong desire to eat very often throughout the week). Higher scores indicate a stronger or more frequent desire to eat during the past week.

Sponsors and collaborators

Lead sponsor

University of Glasgow

Other

Collaborators

  • University of Jazan

Registry information

Official study title

Reproducibility and Agreement of Appetite and Eating Behaviours in Response to Fixed Meals and the Modifying Effect of Feeding Status.

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Dec 2, 2025
Registry last updated
Jun 26, 2026

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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