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Clinical Trials/NCT05672017
NCT05672017CompletedNot Applicable

Sweet Consumption and Subsequent Sweet Food Preferences and Intakes

Bournemouth University1 site in 1 country104 target enrollmentStarted: March 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
104
Locations
1
Primary Endpoint
Sweet Food Preferences

Study Overview

Brief Summary

This study will assess the effects of repeated sweet versus non-sweet food consumption on subsequent sweet and non-sweet food preferences and intakes.

Detailed Description

Participants will be randomized to receive instructions to either increase, decrease or make no change to sweet food consumption for 6 days, and impacts on food preferences and intakes will be assessed at baseline and after 1 week. Preferences for sweet and non-sweet foods will be assessed during a taste test at each assessment time, where six different foods will be rated. Sweet and non-sweet food consumption will also be measured at a subsequent breakfast at the assessment time. Buffet meals composed of sweet and non-sweet foods suitable for consumption at breakfast will be provided ad-libitum.

A subset of participants (selected at random) (10 participants randomized to increase sweet food consumption and 10 participants randomized to decrease sweet food consumption) will also be assessed via MRI and fMRI scanning to investigate brain structure and functional connectivity.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Investigator, Outcomes Assessor)

Masking Description

Investigators, outcome assessors and analysts will be masked. It is not possible to mask participants.

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •aged 18-65 years;
  • •habitually consume breakfast;
  • •able to provide consent and complete all study materials;
  • •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 or within 3 months of starting the study are following a specific dietary programme (e.g.: Slimming World);
  • •current smokers or have smoked within 3 months of the study start date.

Arms & Interventions

Dietary Instructions: Increase sweet food consumption

Active Comparator

Participants are asked to increase their consumption of sweet foods throughout their diet. Participants will be provided with clear instructions, where sweet foods will be highlighted and additional means of increasing sweet food consumption will be offered.

Intervention: Dietary Instructions (Behavioral)

Dietary Instructions: Decrease sweet food consumption

Active Comparator

Participants are asked to decrease their consumption of sweet foods throughout their diet. Participants will be provided with clear instructions, where sweet foods will be highlighted and means of decreasing sweet food consumption will be offered.

Intervention: Dietary Instructions (Behavioral)

Dietary Instructions: Usual Diet

Placebo Comparator

Participants are asked to retain their consumption of sweet foods throughout their diet.

Intervention: Dietary Instructions (Behavioral)

Outcomes

Primary Outcomes

Sweet Food Preferences

Time Frame: Week 1

Preferences for various sweet foods/fluids, assessed using a taste test, where participants sample several sweet and non-sweet foods and rate them for pleasantness on a 100mm Visual Analogue Scale, from 0 to 100mm. Higher scores signify stronger preferences

Sweet Food Choices

Time Frame: Week 1

Selection of sweet foods/fluids at a given meal, assessed where participants can consume freely from a meal composed of sweet and non-sweet foods, and proportion of sweet foods consumed is measured as a percentage of weight consumed

Secondary Outcomes

  • Hunger and Thirst(Week 1)
  • Sweet Food Perceptions(Week 1)
  • MRI Static Brain Scan (Subset of Participants Only)(Baseline to week 1)
  • fMRI Composite Functional Brain Scan (Subset of Participants Only)(Baseline to week 1)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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