ClinicalTrials.gg
Enrolling by invitationNCT06925932Updated Jun 23, 2026

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

An interventional study of Dietary advice - Sweet taste and Dietary advice - Taste in Dietary Behavior, Free Sugar and Sweet Taste, sponsored by Bournemouth University. Enrolling by invitation at 1 site in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-23.

Sponsored by Bournemouth University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
180
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Dietary Behavior
  • Free Sugar
  • Sweet Taste

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Keywords

  • dietary behavior
  • free sugar
  • sweet taste
03

In context

Behavior

1,573 studies on the registry are indexed under Behavior; 313 are open to participants now.

This study's planned enrollment of 180 is above the median of 120 across 1,197 interventional studies indexed under Behavior.

Browse Behavior studies →

Lead sponsor

Bournemouth University is the lead sponsor of 52 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  1. Being a smoker or having smoked in the last 3 months
  2. Being pregnant or breastfeeding
  3. Being underweight ( \< 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
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
180 participants (estimated)

Study arms

  • Active comparator
    Sweet taste arm

    Description: Participants in this arm will be 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.

    Behavioral: Dietary advice - Sweet taste

  • Active comparator
    Taste arm

    Description: Participants in this arm will be 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.

    Behavioral: Dietary advice - Taste

  • Active comparator
    No taste arm

    Description: Participants in this arm will be 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.

    Behavioral: Dietary advice - No taste

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.

06

What researchers measure

Primary outcomes

  1. Free sugar intakes

    Percentage total energy intake (%TEI) from free sugars, measured using multiple 24-hour dietary recalls.

    Time frame: Baseline to week 12

  2. Adherence

    Adherence with the dietary advice received will be assessed by self-report using online surveys.

    Time frame: week 3 to week 12

Secondary outcomes

  1. Energy intake and diet composition

    Energy intake and nutrient composition of dietary intakes, measured using multiple 24-hour dietary recalls.

    Time frame: Baseline to week 12

  2. Body weight

    Weight, in kilograms, assessed using standard digital scales.

    Time frame: Baseline to week 12

  3. Waist circumference

    Waist circumference, in centimeters, measured using standard flexible tape measure.

    Time frame: Baseline to week 12

  4. Body fat percentage

    Body fat percentage assessed using a bioimpedance scale.

    Time frame: Baseline to week 12

  5. Body mass index

    Body mass index assessed using a standard kg/m2 measurement.

    Time frame: Baseline to week 12

  6. Fasted blood glucose

    Fasted blood glucose (min 8h fast), in millimoles per litre, assessed using a prick-a-finger method and a blood glucose monitor.

    Time frame: Baseline to week 12

  7. Sweet food and beverage preferences

    Preferences 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.

    Time frame: Baseline to week 12

  8. Sweet food and beverage perceptions

    Preferences 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.

    Time frame: Baseline to week 12

  9. Sweet food and beverage choice

    Sweet 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.

    Time frame: Baseline to week 12

  10. Dietary advice evaluation

    Evaluation of and perceptions of the dietary advice received will be assessed by self-report using individual questions using online surveys.

    Time frame: week 3 to week 12

  11. Sweet attitudes

    Attitudes 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.

    Time frame: Baseline to week 12

  12. Self-reported quality of life

    Physical and psychosocial functioning will be assessed using the 36-item Short Form Health Survey. Higher scores indicate greater quality of life.

    Time frame: Baseline to week 12

  13. Attitudes towards eating

    General 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.

    Time frame: Baseline to week 12

  14. Dietary knowledge

    Knowledge of dietary and sugar recommendations will be assessed via self-report using specific indvidual questions in an online questionnaire.

    Time frame: Baseline to week 12

  15. Adverse events

    Adverse events will be assessed via self-report.

    Time frame: Baseline to week 12

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started May 2025 (actual). Primary completion is estimated for Dec 2026, 19 months after the start.

Of 741 non-industry interventional studies with no phase under Behavior, half reached primary completion within 14 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 32. This study's planned 19 months is above that.

Counting every sponsor, half of 757 studies reached it within 13 months; a quarter within 5 and three quarters within 32.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 7, 2025
First posted
Apr 13, 2025
StartActual
May 1, 2025
Primary completionEst.
Dec 31, 2026
CompletionEst.
Sep 30, 2027
Last update
Jun 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06925932
Lead sponsor
Bournemouth University
Responsible party
Sponsor
First posted
Apr 13, 2025
Start date
May 1, 2025
Primary completion
Dec 31, 2026 (estimated)
Completion
Sep 30, 2027 (estimated)
Last update
Jun 23, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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