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Clinical Trials/NCT02554162
NCT02554162
Completed
Not Applicable

Chewy Satiety - the Interplay Between Food Structure, Oral Processing and Satiety

VTT Technical Research Centre of Finland1 site in 1 country20 target enrollmentOctober 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Subjective Appetite and Satiety
Sponsor
VTT Technical Research Centre of Finland
Enrollment
20
Locations
1
Primary Endpoint
Postprandial satiety, assessed using 10 cm visual analogue scale (0=not at all, 10=Extremely)
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This study examines if there are differences in satiety responses between structurally different wholegrain rye products.

Detailed Description

The study consists of a satiety trial and mastication trial. The satiety trial consists of five study visits. Five cereal products with berry soup are presented in random order for each subject serving one of them in each study visit (crossover study design). Each meal consists of rye product or wheat bread providing 190 kcal of energy and of 3 dl berry soup (3 dl) providing 140 kcal of energy. The participants are instructed to evaluate their satiety and related sensations before eating the test food, right after eating and then every 30 min until 210 min after breakfast consumption. The evaluated sensations are hunger, fullness, satiety, desire to eat and prospective food consumption ("How much would you be able to eat right now?"), "thirstiness", "mood", "vigourosness" and "pleasantness"."Pleasantness" will be evaluated only right after eating the test food. Cereal food samples with 3-digit number codes will be offered to each participant in a random order in mastication trial. The study products are rye products with varying structures. First the participant is asked to evaluate the expected satiety of the product (How filling would you expect this portion to be on a scale from 0 (=not full at all) to 10 (=extremely full)). Secondly the same food will be served to the participant in three portions and the participant will be asked to masticate each portion until she considers it to be ready for swallowing. Instead of swallowing the bolus will be expectorated to a plastic container which is kept on ice. The mastication process is characterized by measuring electrical activity of facial muscles by electromyography (EMG). The mastication process will be video-recorded to support data handling.

Registry
clinicaltrials.gov
Start Date
October 2015
End Date
December 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Female

Investigators

Sponsor
VTT Technical Research Centre of Finland
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • BMI 18.5-25 kg/m2
  • Habit of eating breakfast

Exclusion Criteria

  • Significant changes in body weight (+ or - 4 kg) during the previous year
  • Pregnant or lactating
  • Missing teeth (except 3rd molars)
  • Acute temporomandibular disorders (TMD)
  • Dietary restrictions possibly affecting the study (celiac disease, allergies or aversions to cereal foods/high carbohydrate foods)
  • Abnormal eating behaviour (according to EDDS (Eating Disorder Diagnostic Scale))

Outcomes

Primary Outcomes

Postprandial satiety, assessed using 10 cm visual analogue scale (0=not at all, 10=Extremely)

Time Frame: In every 30 min until 210 min after consumption

Study Sites (1)

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