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CompletedNCT04138862Updated Oct 28, 2019

The Reduced Calorie Food and Mood Study

An interventional study of Product Labelling and Sensory modifications in Markedly Reduced Food Intake and Satiety and Food Intake, sponsored by Singapore Institute of Food and Biotechnology Innovation. Completed at 1 site in Singapore. Open to participants aged 21 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-10-28.

Sponsored by Singapore Institute of Food and Biotechnology Innovation · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 2 years 1 month after the study started (first participant enrolled Sep 2017, registered Oct 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
121
Allocation
Randomized
Ages
21 Years to 50 Years
Sex
All
01

Study summary

Health- and nutrient-related labelling is often used to draw consumer's attention to the potential benefits of consuming one product over another. However, research suggests that products believed to be 'healthier' and/or lower calorie are often experienced as less satiating, and may actually prompt people to consume more or these foods, or others.

The current research aimed to whether consuming a reduced-calorie product labelled "Healthier Choice" affects compensatory eating behaviour (relative to an unlabelled product), and the extent to which this depends on the product's sensory characteristics.

A two-session randomised study was used to test the satiety value of a reduced-calorie beverage - characterised as changes in rated appetite and later food intake (kcal) relative to an original-calorie version - consumed in one of four contexts varying in label and sensory cues. The beverage-contexts were assessed in a non-crossover manner.

Read the detailed description

Reformulation strategies to reduce the energy density of commonly consumed food and beverage products are needed to support weight management, but one concern is that awareness of consuming 'healthier' foods can promote compensatory eating behaviours. An alternative solution is not to label calorie-reductions so consumers are unaware that they are consuming fewer calories in reformulated products, which has been described as a 'stealth health' approach.

This study investigated whether consuming a reduced-calorie product labelled with Singapore's 'Healthier Choice Symbol' impacts its satiating power relative to an unlabelled control, and the extent to which this can be further modified by changes to the product's sensory characteristics.

Participants were randomised to consume an original (211 kcal per portion; kcal/g) and reduced calorie (98 kcal per portion; kcal/g) versions of a soymilk, with the reduced calorie version presented in one of four beverage context conditions:

  • Context 1 - Sensory-matched, unlabelled calorie reduction (control) - Sensory matched to taste like the original (equally sweet, thick and creamy), without a label identifier (covert energy reduction).
  • Context 2 - Sensory-matched, labelled calorie reduction - The same sensory matched beverage as above, but with the HCS attached (explicit energy reduction).
  • Context 3 - Sensory-reduced, labelled calorie reduction - Designed to taste less thick, sweet and creamy than the original, with the HCS attached (explicit energy reduction).
  • Context 4 - Sensory-enhanced, labelled calorie reduction - Designed to taste thicker, creamier and sweeter than the original, with the HCS attached (explicit energy reduction).

Participants consumed the two beverages (original vs. reduced energy) in one of the four beverage contexts on two non-consecutive test sessions at the Clinical Nutrition Research Centre, with at least three days washout between each session. The calorie reduction was conducted as full-crossover while the beverage context groups were assigned non-crossover, to reduce demand awareness.

The primary objective was to assess changes in lunch energy intake (kcal) after consuming the original and reduced-calorie beverages, depending on the beverage context the reduced calorie version was presented in.

The secondary objectives were to assess the sensory evaluations of the beverages (liking and perceived thickness, sweetness and expected fullness etc.), changes in rated appetite up to 180 minutes post-consumption and energy intake (kcal) for the rest of the test day (recorded in a food diary), as a function of the beverages energy density and context.

02

Conditions studied

  • Markedly Reduced Food Intake
  • Satiety and Food Intake
03

In context

Lead sponsor

Singapore Institute of Food and Biotechnology Innovation is the lead sponsor of 69 studies on the registry; 4 are open to participants now.

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

04

Who can participate

Ages eligible
21 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Aged between 21 and 50 years
  • English Speaking

Exclusion criteria

Exclusion Criteria:

  • People who are taking insulin or medications known to affect glucose metabolism, appetite or energy metabolism
  • Individuals who are currently following a diet program
  • People with intolerances or allergies to study foods or test products, e.g. soya, wheat, gluten, cereal, fruits, biscuits, dairy products, rice, vegetable, meat, seafood, sugar and sweetener, gelatin, natural food colourings or flavourings, etc
  • Pregnant women
  • Regular smokers (> 5 cigarettes per week)
  • Individuals with body mass index (BMI) \< 18.5 and > 30.0 kg/m2
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Single (Participant)
Enrollment
121 participants (actual)

Study arms

  • Active comparator
    Sensory Matched/Unlabelled

    Sensory-matched covert calorie reduction, unlabelled

    Behavioral: Product Labelling and Sensory modifications

  • Experimental
    Sensory Matched/Labelled

    Sensory-matched explicit calorie reduction, labelled

    Behavioral: Product Labelling and Sensory modifications

  • Experimental
    Sensory Reduced/Labelled

    Sensory-reduced explicit calorie reduction, labelled

    Behavioral: Product Labelling and Sensory modifications

  • Experimental
    Sensory Enhanced/Labelled

    Sensory-enhanced explicit calorie reduction, labelled

    Behavioral: Product Labelling and Sensory modifications

Interventions

  • BehavioralProduct Labelling and Sensory modifications

    the beverages varied in the label that was attached (no label or a 'Healthier Choice' label) and the sensory matching of the calorie reduction (sensory matched, reduced or enhanced).

06

What researchers measure

Primary outcomes

  1. Ad libitum intake of a later lunch meal (calories - kcal)

    The weight of the test meal consumed during the test session was measured. - There are four test sessions and participants eat one of the four test meals each session. The amount consumed was measured each time.

    Time frame: Measured once for up to 20 minutes

Secondary outcomes

  1. Changes in rated appetite pre- to post beverage and up to 180 minutes post-consumption, all prior to consuming an ad libitum lunch

    100-point Visual Analogue Scale (VAS) ratings of hunger, fullness, desire to eat, prospective consumption and thirst.

    Time frame: pre-meal, immediately post-meal, +15 minutes, +30 minutes, +45 minutes, +60 minutes, +75 minutes, + 90 minutes, + 120 mins, + 150 mins + 180 mins

  2. Sensory ratings after the first sip of the test beverage

    100-point Visual Analogue Scale (VAS) ratings of thick, sweet, liking, creamy, chalky and sour.

    Time frame: Measured once upon first tasting the test beverage for up to 5 minute

  3. Energy intake (kcal) for across the test day recorded in a Food diary

    Food intake recorded in a food diary and analysed by a trained research assistant using FoodWorks 8.0.3553.

    Time frame: Up to 24 hours

07

Study locations

1 site
  • Clinical Nutrition Research Centre
    Singapore, 117599, Singapore
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 28, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04138862
Lead sponsor
Singapore Institute of Food and Biotechnology Innovation
Responsible party
Keri McCrickerd (Senior Research Fellow, Singapore Institute of Food and Biotechnology Innovation) — Principal investigator
First posted
Oct 25, 2019
Start date
Sep 9, 2017
Primary completion
Sep 9, 2018
Completion
Sep 20, 2019
Last update
Oct 28, 2019

Study contacts

Keri McCrickerd, PhD
principal investigator · Clinical Nutrition Research Centre

Oversight

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

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