CompletedNot Applicable

The Impact of Snacks Which Vary Nutritionally in Their Satiating Potential on Measures of Appetite Control

42 participantsStarted 2015-06

Plain-language summary

The current study will examine the effect of almond consumption (0.9g/kg dose) compared to an energy and weight matched comparator food or no food on measures of appetite control including appetite sensations, energy intake and food hedonics.

Who can participate

Age range

18 Years – 55 Years

Sex

FEMALE

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: * Participants who have provided written informed consent. * Healthy female participants aged 18-55 years. * BMI of 18.5 - 30.0 kg/m2. * Regular breakfast eaters. * Not currently dieting to lose, gain or maintain weight. * Non-smokers. * Liking/acceptance of the study foods (≥4 on 7-point Likert scale). Exclusion Criteria: * Taking medication known to affect appetite within past month and/or during the study. * Any known food allergies or food intolerances. * Participants who do not regularly eat breakfast. * Participants with low liking or acceptance of the study foods. * Participants currently dieting to lose, gain or maintain weight. * Reported history of or present eating disorder. * BMI \<18.5 kg/m2 or \>30 kg/m2. * Vegetarians.

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.

What they're measuring

Test Meal Energy Intake

Timeframe: 3 Weeks

Trial details

NCT IDNCT02480582

SponsorUniversity of Leeds

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-11

Results submitted2016-05-31

View on ClinicalTrials.gov More Lack of Satiety trials