The Effect of Meal Texture on Intake (NCT05615350) | Clinical Trial Compass
CompletedNot Applicable
The Effect of Meal Texture on Intake
Netherlands30 participantsStarted 2022-10-24
Plain-language summary
In this study the effect of meal texture differences (slow vs fast eating rate) on intake will be investigated.
Who can participate
Age range
18 Years – 55 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Generally healthy
* Good appetite
* Between 18 and 55 years old
* Speak and understand English without difficulty
* BMI between 18.5-30 kg/m2.
* Non-smoker
* Commonly (5 out of 7 week days) eat three meals a day every day around the
Exclusion Criteria:
* Have difficulties with swallowing, chewing, and/or eating in general;
* Are suffering from an endocrine or eating disorder, gastrointestinal illness or illness of the thyroid gland, respiratory disease, or diabetes
* Have taste or smell disorders
* Have braces or oral piercing (dental wire behind teeth is allowed)
* are smoking
* Consume on average more than 21 glasses of alcohol per week
* Are not willing to stop using drugs during the study period (from inclusion till last test session)
* Use medication that may influence study outcomes
* Have allergies or intolerance to any ingredient of the test meals
* Are not willing to eat the test food because of eating habits, believes, or religion
* Follow a vegetarian or vegan diet
* Are lactose intolerant
* Have facial hair such as a beard
* Follow an energy restricted diet during the last 2 months
* Gained or lost 5 kg of body weight over the last half year
* Are an employee, thesis student or intern at the chair group of Sensory Science and Eating Behaviour Human Nutrition (WUR).
* Do intensive exercising more than 8 hours per week
* Low score (\<1) for liking the individual test meals on a nine point Likert scale based on pictures of the meals
* Familia…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.