Opportunities for Food Reformulation (OffR)

December 12, 2022 updated by: Marlou Lasschuijt, Wageningen University

Opportunities For Food Reformulation: Food Texture and Energy Density Effects on Eating Behaviour and Satiation

The objective of this study is to determine the independent and additive effects of food texture and energy density on food and energy intake compared to a control condition.

Study Overview

Detailed Description

Study design: The study has a 2x2 randomized crossover design. All participants receive 5 treatments and are their own control.

Study population: Healthy adults (n=75) between 18-55 years old with a BMI between 18.5-30 kg/m2.

Intervention: Participants will join 5 test days during which they receive, 5 test meals (lunch). The 5 test meals of this study are: 1.) low energy density, hard texture (slow eating rate) 2.) low energy density, soft texture (fast eating rate) 3.) High energy density, hard texture (slow eating rate) 4.) High energy density, soft texture (fast eating rate) 5.) Average energy density and medium hard texture (control). During eating and before and after eating the weight of the plate will be measured to determine intake. Additionally, participants will be recorded on video to determine eating behaviour (number of bites, chews and oral processing duration). The order in which participants will receive the diets will be randomized. The evening before and during each test day participants will keep a food and exercise diary.

Main study parameters/endpoints: The main study outcomes are food and energy intake of each lunch meal. Secondary outcomes are, eating behaviour characteristics measured by video (eating rate (g/min and bites/min), number of chews (chews/bite and chews/gram), bite size (gram/bite), oral processing duration (seconds), appetite (hunger, fullness, desire to eat, desire to eat sweet, desire to eat savoury, prospective consumption) and sensory characteristics (liking (taste + smell), desire to eat the meal, expected satiation, sweet, savoury, smoothness, chewiness, thickness) of the meals. Additional outcomes are individual differences in microstructure of eating, appetite responsiveness, eating Behavior phenotype, interoceptive sensitivity and anthropometry measures. During the trial new technology to capture food intake and eating behavior will be validated which is also an outcome of this trial.

Study Type

Interventional

Enrollment (Actual)

75

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Gelderland
      • Wageningen, Gelderland, Netherlands, 6708WE
        • Wageningen University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years to 51 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Between 18-55 years old at the day of inclusion
  • Able to understand and speak English fluently or without difficulty (self-report)
  • BMI 18.5-30 kg/m2 - measured by the researchers at the end of information meeting
  • Good general health and appetite ( self-report)
  • Commonly (5 out of 7 week days) eating three meals a day every day around approximately the same times(Self-report).

Exclusion Criteria:

  • Difficulties with swallowing, chewing and or eating in general
  • Suffering from an endocrine or eating disorder, gastrointestinal illness or illness of the thyroid gland, respiratory disease or diabetes.
  • Having taste or smell disorders (self-report)
  • Braces (not including a dental wire) or oral piercing
  • Smoking
  • Consuming on average more than 21 glasses of alcohol per week (21)
  • Not willing to stop using drugs during the study period (from inclusion till last test session)
  • Use of medication that may influence study outcomes (self-report)
  • Allergies or intolerance to any ingredient of the test meals or snacks
  • Not willing to eat the test food because of eating habits, believes or religion.
  • Following a vegetarian or vegan diet
  • Lactose intolerant
  • Men having facial hair such as a beard as facial movements cannot be analysed.
  • Followed an energy restricted diet during the last 2 months
  • Gained or lost 5 kg of body weight over the last half year
  • High restrained eater according to the Dutch Eating Behaviour Questionnaire (men: score>2.89, women>3.39 )
  • Signed up for participating in another research study
  • Employee of Human Nutrition department of Wageningen university
  • Thesis student or intern at the chair group of Sensory Science and Eating Behaviour Human Nutrition (WUR).
  • Intensive exercising more than 8 hours per week
  • Low score for liking the test foods on a nine point likert scale based on pictures of the food items.
  • Unfamiliar with the test foods (self-report).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: low energy density, hard texture
Sandwich with a hard texture (slow eating rate) and relatively low energy density (kcal/g)
Food properties of commercially available food products
Experimental: low energy density, soft texture
Sandwich with a soft texture (fast eating rate) and relatively low energy density (kcal/g)
Food properties of commercially available food products
Experimental: High energy density, hard texture
Sandwich with a hard texture (slow eating rate) and relatively high energy density (kcal/g)
Food properties of commercially available food products
Experimental: High energy density, soft texture
Sandwich with a soft texture (fast eating rate) and relatively high energy density (kcal/g)
Food properties of commercially available food products
Active Comparator: Average energy density and medium hard texture (control)
Sandwich with a medium texture (medium eating rate) and medium energy density (kcal/g)
Food properties of commercially available food products

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Energy intake
Time Frame: One meal, up to 30 minutes
Intake in Kcal
One meal, up to 30 minutes
Food intake
Time Frame: One meal, up to 30 minutes
Intake in gram
One meal, up to 30 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Eating rate
Time Frame: One meal, up to 30 minutes
Eating rate gram/min
One meal, up to 30 minutes
chews
Time Frame: One meal, up to 30 minutes
number of chews per bite
One meal, up to 30 minutes
bite size
Time Frame: One meal, up to 30 minutes
gram/bite
One meal, up to 30 minutes
Energy intake rate
Time Frame: One meal, up to 30 minutes
kcal/min
One meal, up to 30 minutes
bites
Time Frame: One meal, up to 30 minutes
number of bites per meal
One meal, up to 30 minutes
swallows
Time Frame: One meal, up to 30 minutes
number of swallows per meal
One meal, up to 30 minutes
oral exposure time
Time Frame: One meal, up to 30 minutes
duration of food in mouth in seconds
One meal, up to 30 minutes
Appetite
Time Frame: One meal, up to 30 minutes
subjective ratings of appetite on a 100 mm line scale (visual analogue scale)
One meal, up to 30 minutes
Individual differences in fat free mass (FFM)
Time Frame: 5 minutes
% FFM of total body weight
5 minutes
individual eating rate
Time Frame: 1 minute
eating rate (gram/min) of carrots of each participant (personal trait)
1 minute
Individual appetite responsiveness
Time Frame: 10 minutes
interoceptive sensitivity the ratio between the amount drank till first satiation signal and complete fullness, according to the waterload test
10 minutes
Sensory properties
Time Frame: 5 minutes
rating on a 100mm line scale (visual analogue scale from 0 - not at all to 100 extremely) of the sensory properties of the sandwiches offered during the test sessions
5 minutes

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
technology to measure intake automatically
Time Frame: One meal, up to 30 minutes
automated weighing scales
One meal, up to 30 minutes
technology to measure eating behavior
Time Frame: One meal, up to 30 minutes
automated measures of eating behavior using video recordings
One meal, up to 30 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 22, 2022

Primary Completion (Actual)

July 8, 2022

Study Completion (Actual)

July 8, 2022

Study Registration Dates

First Submitted

May 2, 2022

First Submitted That Met QC Criteria

December 12, 2022

First Posted (Actual)

December 21, 2022

Study Record Updates

Last Update Posted (Actual)

December 21, 2022

Last Update Submitted That Met QC Criteria

December 12, 2022

Last Verified

December 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • offR WUR

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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