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This Trial Aims to Assess the Effects of Three Different Taste-based Dietary Recommendations for Reducing Free Sugar Intakes on Free Sugar Consumption in UK High Free Sugar Consumers

Reducing Free Sugar Intakes - The Role of Sweet Taste III

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06925932
Enrollment
180
Registered
2025-04-13
Start date
2025-05-01
Completion date
2027-09-30
Last updated
2026-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dietary Behavior, Free Sugar, Sweet Taste

Keywords

dietary behavior, free sugar, sweet taste

Brief summary

This randomised controlled trial aims to assess the effects of three different taste-based dietary recommendations for reducing free sugar intakes on free sugar consumption in UK high free sugar consumers.

Detailed description

This 12-week, 3-arm randomised controlled trial aims to assess the effects of three different taste-based food and beverage substitution instructions for reducing free sugar intakes on free sugar consumption in high free sugar consumers. A total of 180 adult community members residing in Bournemouth and the surrounding areas will be recruited. All participants will be asked to reduce their intakes of free sugar and replace sweet, high-free sugar foods and beverages with either: 1) sweet tasting foods and beverages that have no or low amounts of free sugars; 2) non-sweet tasting foods and beverages that have no or low amounts of free sugars and are high in other tasty flavours; and 3) non-sweet tasting foods and beverages that have no or low amounts of free sugars and are also low in other flavours. The primary outcome of interest is the changes in free sugar intakes from baseline to endpoint. Secondary outcomes include a range of dietary and biopsychosocial outcomes, sweet taste perceptions and sweet food and beverage intakes, as well as compliance with and evaluation of the dietary recommendation received.

Interventions

BEHAVIORALDietary advice - Sweet taste

Asked to reduce their free sugar intakes to \< 5%TEI and replace sweet foods and drinks that are high in free sugars with foods and drinks that are sweet but have no or low amounts of free sugars, e.g., sweet no- or low-free sugar foods, fruit, and no- or low-calorie sweeteners.

BEHAVIORALDietary advice - Taste

Asked to reduce their free sugar intakes to \< 5%TEI and replace sweet foods and drinks that are high in free sugars with foods and drinks that are non-sweet but are full of tasty flavours, e.g., non-sweet foods and drinks with nuts, herbs or spices.

BEHAVIORALDietary advice - No taste

Asked to reduce their free sugar intakes to \< 5%TEI and replace sweet foods and drinks that are high in free sugars with foods and drinks that are non-sweet and have no strong flavours, e.g., non-sweet plain foods and drinks.

Sponsors

Bournemouth University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

The investigator and all outcome assessors will be blinded to the intervention allocation. Participants will also be blinded to intervention allocation aside from their own. Data processing and analysis will be undertaken in a blinded manner.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Age 18 and over 2. Consuming more than 10% total daily energy from free sugars (-3% for testing error) 3. Residing in the South of England, and able to attend Bournemouth University for testing (Talbot Campus, BH12 5BB) 4. Able to provide consent and complete all study-related measures

Exclusion criteria

1. Being a smoker or having smoked in the last 3 months 2. Being pregnant or breastfeeding 3. Being underweight (BMI \< 18.5 kg/m²) 4. Dieting or following a specific diet program (e.g., Weight Watchers, Keto diet, or Intermittent Fasting) 5. Following a specific diet or nutritional advice as a result of pre-existing medical condition (e.g., Crohn's disease, diabetes) 6. Having a pre-existing medical condition or taking medication that could affect taste and/or smell abilities (e.g., certain blood pressure and heart medications) 7. Allergies to foods and drinks used in the study

Design outcomes

Primary

MeasureTime frameDescription
Free sugar intakesBaseline to week 12Percentage total energy intake (%TEI) from free sugars, measured using multiple 24-hour dietary recalls.
Adherenceweek 3 to week 12Adherence with the dietary advice received will be assessed by self-report using online surveys.

Secondary

MeasureTime frameDescription
Energy intake and diet compositionBaseline to week 12Energy intake and nutrient composition of dietary intakes, measured using multiple 24-hour dietary recalls.
Body weightBaseline to week 12Weight, in kilograms, assessed using standard digital scales.
Waist circumferenceBaseline to week 12Waist circumference, in centimeters, measured using standard flexible tape measure.
Body fat percentageBaseline to week 12Body fat percentage assessed using a bioimpedance scale.
Body mass indexBaseline to week 12Body mass index assessed using a standard kg/m2 measurement.
Fasted blood glucoseBaseline to week 12Fasted blood glucose (min 8h fast), in millimoles per litre, assessed using a prick-a-finger method and a blood glucose monitor.
Sweet food and beverage preferencesBaseline to week 12Preferences for sweet foods and beverages will be assessed using a taste perception test. Participants will taste commercially available several sweet and non-sweet foods and beverages and indicate how pleasant these are and how much they desire to eat these using 0-100 visual analogue scales. Higher scores indicate greater pleasantness and desire to eat.
Sweet food and beverage perceptionsBaseline to week 12Preferences of the sweet taste intensity will be assessed using a taste perception test. Participants will taste several commercially available sweet and non-sweet foods and beverages and indicate their sweetness intensity using 0-100 visual analogue scales. Higher scores indicate greater perceived sweetness intensity.
Sweet food and beverage choiceBaseline to week 12Sweet food and beverage choice will be assessed using a breakfast meal. A wide selection of commercially available sweet and non-sweet breakfast foods and beverages will be presented, with participants free to choose what and how much they consume. Sweet food and beverage choices will be measured as the weight consumed during the breakfast meal. A take-home beverage will also be offered from a selection of sweet and non-sweet beverages with the choice recorded.
Dietary advice evaluationweek 3 to week 12Evaluation of and perceptions of the dietary advice received will be assessed by self-report using individual questions using online surveys.
Sweet attitudesBaseline to week 12Attitudes toward sugars, sweeteners, and sweet foods will be assessed using the Sweet Talk Questionnaire in six domains. The higher the score in a given domain, the more prevalent the attitude.
Self-reported quality of lifeBaseline to week 12Physical and psychosocial functioning will be assessed using the 36-item Short Form Health Survey. Higher scores indicate greater quality of life.
Attitudes towards eatingBaseline to week 12General attitudes towards eating will be assessed using the Dutch Eating Behaviour Questionnaire in three domains. The higher the score in a given domain, the more prevalent the behaviour.
Dietary knowledgeBaseline to week 12Knowledge of dietary and sugar recommendations will be assessed via self-report using specific indvidual questions in an online questionnaire.
Adverse eventsBaseline to week 12Adverse events will be assessed via self-report.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 24, 2026