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Dietary Recommendations for Reducing Free Sugar Intakes

Not Applicable
Completed
Conditions
Dietary Recommendations
Interventions
Behavioral: Dietary recommendations
Registration Number
NCT04816955
Lead Sponsor
Bournemouth University
Brief Summary

This randomised controlled trial aims to assess the impacts of the current recommendations by Public Health England for reducing free sugar intakes, on total energy intakes of free sugar in a sample of the UK population.

Detailed Description

The primary objective of this randomised control trial is to assess the impacts of Public Health England's (PHE) current free sugar reducing advice, for reducing total energy intakes (TEI) of free sugar. A total of 240 participants (age 18-65years) consuming diets \>5% total energy intake from dietary free sugars will be recruited from across the Dorset region. Participants to be randomly assigned into the following recommendation interventions groups: 1) Reduce free sugar intake to \<5% TEI (nutrient-based recommendations); 2) Reduce free sugar intake to \<5% TEI, via reducing intake of specific foods identified as high in free sugars (nutrient- + food-based recommendations); 3) Reduce free sugar intake to \<5% TEI, via reducing intake of specific foods identified as high in free sugars and replace/swap with low sugar versions (nutrient- + food-based recommendations with swaps); and 4) Control Group. The primary outcome will be changes in free sugar consumption from baseline to endpoint at week 12. Secondary outcomes include change in: BMI; dietary profiles; sweetness preference; sweetness liking; food choices; low calorie sweetener intakes and adherence levels.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
242
Inclusion Criteria
  • aged 18-65 years;
  • able to provide consent and complete all study materials;
  • consuming >5% of TEI from free sugars; and
  • residing in the South of England.

Exclusion criteria:

  • individuals who are pregnant or breastfeeding;
  • underweight (BMI <18.5);
  • 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;
  • 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.
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Nutrient-based recommendationsDietary recommendationsParticipants in this group will be given nutrient-based recommendations to reduce free sugar intakes.
Nutrient- and food-based recommendationsDietary recommendationsParticipants in this group will be given nutrient- and food-based recommendations to reduce free sugar intakes.
Nutrient- and food-based recommendations with food swapsDietary recommendationsParticipants in this group will be given nutrient- and food-based recommendations and advice on food swaps to reduce free sugar intakes.
ControlDietary recommendationsParticipants in this group will not be given any recommendations to reduce free sugar intakes.
Primary Outcome Measures
NameTimeMethod
Free sugar intakes12 weeks from baseline

Percentage energy intake from free sugars, assessed using diet diaries

Adherence12 weeks from baseline

Adherence to the recommendations provided, assessed using diet diaries and self-reported adherence

Secondary Outcome Measures
NameTimeMethod
Adverse eventsBaseline to 12 weeks

Adverse events, assessed by self-report

Eating-based motivationsBaseline to 12 weeks

Motivations towards eating, assessed using the Food Choice Questionnaire (Steptoe et al., Appetite 1995, 25(3): 267-84). Higher scores denote stronger motivations

Quality of Life (subjective wellbeing)Baseline to 12 weeks

Quality of Life, measured using the SF-36 questionnaire (Ware et al, 1996), where Quality of Life is assessed out of 100, where a higher score demonstrates better quality of life

Dietary intakes12 weeks from baseline

Nutrient composition of dietary intakes, assessed using diet diaries

BMI12 weeks from baseline

Body Mass Index, assessed using researcher measurements or researcher-observed self-measurements

Eating-based attitudesBaseline to 12 weeks

Attitudes towards eating, assessed using the Three Factor Eating Questionnaire (Karlsson J, et al. IJO 2000; 24: 1715-1725)

Sweet food preferences12 weeks from baseline

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. Higher scores signify stronger preferences

Sweet food choices12 weeks from baseline

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 in terms of weight consumed

Sweet food attitudes12 weeks from baseline

Attitudes towards sugar, sweeteners, and sweet-tasting foods, assessed using a questionnaire, soon to be published. Higher scores denote stronger attitudes.

Trial Locations

Locations (1)

Bournemouth University

🇬🇧

Bournemouth, US And Canada Only, United Kingdom

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