The Lunch Study: the Combined Effects of Food Texture and Portion Size on Intake

Sponsor
Clinical Nutrition Research Centre, Singapore (Other)
Overall Status
Completed
CT.gov ID
NCT02977273
Collaborator
(none)
53
1
4
12
4.4

Study Details

Study Description

Brief Summary

Meal size is strongly influenced by a number of external features of the food environment which can promote over-consumption, such as the availability of palatable energy dense foods and large portion sizes. The current research aimed to investigate whether natural food-based differences in texture could be used to slow down eating rate and reduce intake from large portions.

A four-session randomised crossover study assessed the effect of faster vs. slower eating rate, achieved through manipulating food texture, on ad-libitum consumption (weight and calories) of a meal, alone and in combination with variations in meal portion size (regular vs. large)

Condition or Disease Intervention/Treatment Phase
  • Other: Thin/100% Portion
  • Other: Thin/150% Portion
  • Other: Thick/100% Portion
  • Other: Thick/150% Portion
N/A

Detailed Description

The current obesogenic environment is characterized by the abundance of palatable and high energy dense foods. Eating from large portions can promote sustained overcompensation at meal times. On the other hand, eating at a slower rate has been shown to reduce meal size, and food-based texture differences can slow eating rate. It is possible that texture-based differences in eating rate could be used to reduce energy intake in of foods that are served in large portions.

This study was conducted to quantify the effect of eating rate (fast vs. slow) on ad-libitum consumption of a meal, alone and in combination with variations in portion size (100 % 700 g vs 150 % 1050 g). The meal combinations were as follows:

Meal 1: thin/100% portion; Meal 2: thin/150% portion; Meal 3: thick/100% portion; Meal 4:

thick /150% portion

Participants consumed the four test meals over four non-consecutive test sessions at the Clinical Nutrition Research Centre, with at least three days washout between each session. Each part followed a completely randomised full crossover design.

The primary objective was to assess ad libitum intake (both kcal and g) of the test meals, depending on the combination of food texture and energy density.

The secondary objectives were to assess the eating rate, oral processing characteristics, changes in rated appetite up to 90 minutes post-consumption and energy intake (kcal) for the rest of the test day (food diary), as a function of the test meal texture and energy density

Study Design

Study Type:
Interventional
Actual Enrollment :
53 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Basic Science
Official Title:
The Lunch Study: the Combined Effects of Food Texture and Portion Size on Intake
Study Start Date :
Sep 1, 2015
Actual Primary Completion Date :
Sep 1, 2016
Actual Study Completion Date :
Sep 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Test Meal 1

Thin/100% portion

Other: Thin/100% Portion
Thin textured rice meal (ground rice grains) served in a regular portion size (100 %: 700g)

Experimental: Test Meal 2

Thin/150% portion

Other: Thin/150% Portion
Thin textured rice meal (ground rice grains) served in a larger portion size (150 %: 1050g)

Experimental: Test Meal 3

Thick/100% Portion

Other: Thick/100% Portion
Thick textured rice meal (whole rice grains) served in a regular portion size (100 %: 700g)

Experimental: Test Meal 4

Thick/150% Portion

Other: Thick/150% Portion
Thick textured rice meal (whole rice grains) served in a larger portion size (150 %: 1050g)

Outcome Measures

Primary Outcome Measures

  1. Ad libitum intake of the test meals - weight (g) [Measued once for up to 20 minutes]

    The weight of the test meal that is consumed during the 20 minute session was recorded. There are four test sessions and participants eat one of the four test meals each session. The amount consumed was measured each time.

  2. Ad libitum intake of the test meals - calories (kcal) [Measued once for up to 20 minutes]

    The weight of the meal consumed at each of the four test sessions was convert to calories using the meal energy density (which is known). There are four test sessions and participants eat one of the four test meals each session. The amount consumed was measured each time.

Secondary Outcome Measures

  1. Eating rate of the test meal [Measued once for up to 20 minutes]

    Video recordings of the participants eating are coded and from this eating rate was calculated as grams consumed per minute (g/min).

  2. Changes in rated appetite pre- to post meal consumption and up to 90 minutes post-consumption [pre-meal, immediately post-meal, +15 minutes, +30 minutes, +45 minutes, +60 minutes, +75 minutes, + 90 minutes]

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

  3. Energy intake (kcal) for the rest of the test day recorded in a Food diary [Up to 24 hours]

    Food intake recorded in a food diary

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 50 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion criteria:
  • Aged between 21 and 50 years

  • BMI < 30 kg/m2

Exclusion criteria:
  • Individuals whose body weight has changed more than 5 kilograms in the last 12 months

  • People who are taking insulin or medications known to affect glucose metabolism, appetite or energy metabolism

  • Individuals who are currently dieting

  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinical Nutrition Research Centre Singapore Singapore 117599

Sponsors and Collaborators

  • Clinical Nutrition Research Centre, Singapore

Investigators

  • Principal Investigator: Keri McCrickerd, PhD, Clinical Nutrition Research Centre

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Keri McCrickerd, Dr Keri McCrickerd, Clinical Nutrition Research Centre, Singapore
ClinicalTrials.gov Identifier:
NCT02977273
Other Study ID Numbers:
  • 2015/00867 Part 2
First Posted:
Nov 30, 2016
Last Update Posted:
Nov 30, 2016
Last Verified:
Nov 1, 2016
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Keri McCrickerd, Dr Keri McCrickerd, Clinical Nutrition Research Centre, Singapore

Study Results

No Results Posted as of Nov 30, 2016