CompletedNot Applicable

Reducing Free Sugar Intakes: A Role for Sweet Taste

United Kingdom29 participantsStarted 2023-03-01

Plain-language summary

This randomised controlled trial aims to assess the effects of three different types of dietary advice for reducing free sugar intakes, on intakes of free sugar, in a sample of the UK population.

Who can participate

Age range

18 Years – 65 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

. aged 18-65 years;
. able to provide consent and complete all study materials;
. consuming \>5% of TEI from free sugars;
. residing in the South of England, and able to attend Bournemouth University for testing.

Exclusion criteria

. individuals who are pregnant or breastfeeding;
. underweight (BMI \<18.5);
. have pre-existing clinical conditions such as diabetes mellitus, eating disorders, Crohn's disease and other illness's leading to participants receiving external nutritional advice and dietary restrictions;
. have pre-existing medical conditions affecting swallow ability, taste and smell perception;
. currently following a specific dietary programme (e.g.: Slimming World);
. current smokers or have smoked within 3 months of the study start date.

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

Free sugar intakes

Timeframe: Baseline to week 12

Adherence

Timeframe: Baseline to week 12

Trial details

NCT IDNCT05684757

SponsorBournemouth University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-12-22

View on ClinicalTrials.gov More Dietary Behaviour trials