Cricket Flour Metabolism in Humans (InsectGEP)

January 13, 2025 updated by: University of Surrey

With increasing demands on the environment people are looking in different ways to decrease their carbon footprint. Protein is an important part of human diets a it provides building blocks for growth and helps to ensure people stay health. Animal protein is one of the primary sources of of protein from our diets but it is also known that farming cattle for example places a lot of pressure on the environment. As a result of this new protein sources are being looked at that can take the place of animal protein. Insects have been consumed on many civilisations for a long time and they are slowly making their way into the western diets.

At this time the investigators however do not know very much about how well insect protein compares to animal protein as a nutritious food source. This research project is therefore one of the first to compare some of the nutritional properties between animal and insect proteins.

In brief, this study involves eating a sweet breakfast muffin made of either whey (animal) protein powder or cricket flour (very finely ground whole adult crickets) and then breathing into test tubes at various time points for a few hours as well as collecting some small amounts of blood using a finger stick to measure blood glucose and fats.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Insects have been used as protein source for many years in East-Asian and African populations, and more recently the interest in this potential protein source has been growing in Western countries due to the issues outlined above and increased awareness of animal welfare issues in the food chain. However, up until now there is no clear evidence that insect-derived protein has the same nutritional properties as its animal counterpart. Even though nutritional composition of insects can be similar or sometimes even better to support a healthy diet certain properties of the insects (such as the chitin in their exoskeleton) could have detrimental effects on their bioavailability. Gastric emptying (GE) describes the process of food being digested and absorbed by the controlled delivery from the stomach into the duodenum (1.). In the field of nutrition, GE is important, since a slower rate of GE can lead to a lower postprandial rise in macronutrients, and consequently a lower postprandial burden on their clearance. To date it is known that certain food properties such as volume, calories, and viscosity, as well as physiological factors such as age and gender can influence the gastric emptying rate (1.). However, the interaction between human physiology and different food in the stomach is widely unknown.

A slower GE rate is particularly important regarding postprandial plasma triacylglycerol concentrations, with impaired clearance being related to inflammation and cardiovascular disease. The attenuation of the postprandial increase in blood glucose has long been a goal for improved metabolic health. As reviewed, small differences in GE can have a major impact on postprandial glycaemia in health and type 2 diabetes (2.). Furthermore, a slowed gastric emptying rate as a result of certain types of food is associated with a delayed reoccurrence of feeling of hunger and can influence satiation.

The 13C octanoic acid breath test is a relatively cheap, non-invasive, and simple test to measure GE. The test is performed via the ingestion of a controlled meal containing the commercially available non-harmful stable isotope 13C in a short chain fatty acid (C8) and the following detection of the 13Clabelled CO2 in the breath (3.).

The data generated by the breath test is commonly analysed with a one compartment model based on Ghoos et al (1993) (4.) to generate parameters such as half time and lag time. More advanced semi mechanistic models are used in pharmacokinetics and could be applied to the breath test.

Study Type

Interventional

Enrollment (Actual)

10

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

    • Surrey
      • Guildford, Surrey, United Kingdom, GU2 7XH
        • University of Surrey

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Apparently healthy adult males and females between 20 and 55 years of age

    • BMI between 18.5 and 35 kg/m2
    • Weight stable for 3 months (± 2 kg)
    • Volunteers must be able and willing to give informed written consent
    • Volunteers must be able to eat egg (because egg is required for preparation of the stable isotope dosage see section experimental design).

Exclusion Criteria:

  • Previous or current medical conditions, including heart disease, diabetes, gastrointestinal diseases (for example Crohn's disease, Coeliac disease, Inflammatory Bowel Disease), liver disease, endocrine diseases - assessed via a health questionnaire (appendix)
  • Those taking (or have been taking within the past 6 months) regular medication, excluding contraceptive medication, or food supplements (e.g., vitamins, minerals, fish oil, fibre supplements, antioxidant tablets) - assessed via a health questionnaire (appendix) Those smoking, using nicotine products (e.g., e-cigarettes, patches) or not abstained from these activities for more than 6 months
  • Pregnant or lactating
  • Volunteers with a habitual caffeine intake > 300 mg/day (more than 5 cups standard coffee)
  • Drug or alcohol abuse in the last 2 years
  • The principal investigator considers it unsafe / unsuitable for the volunteer to be in the study
  • Those who are currently taking part in a clinical trial or another research study or have taken part within the last 3 months
  • Those who do not refrain from alcohol, caffeine containing drinks (e.g., coffee, coca cola, tea, Red Bull) and strenuous exercise 10 hours before the laboratory session
  • Those with food allergies, dietary intolerance (especially for egg), or Coeliac disease
  • Those following weight reducing diets

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: Control
Whey Protein intervention
Participants are provided with muffins containing either whey or cricket protein.
Experimental: Insect
Cricket Protein intervention
Participants are provided with muffins containing either whey or cricket protein.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Digestion
Time Frame: 4 hours post prandial
Gastric emptying
4 hours post prandial

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Digestion
Time Frame: 4 hours post prandial
T lag
4 hours post prandial
Blood metabolites
Time Frame: 4 hours post prandial
Glucose
4 hours post prandial
Blood metabolites
Time Frame: 4 hours post prandial
Cholesterol
4 hours post prandial

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)

October 1, 2022

Primary Completion (Actual)

August 1, 2023

Study Completion (Actual)

January 8, 2025

Study Registration Dates

First Submitted

January 7, 2025

First Submitted That Met QC Criteria

January 7, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 13, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • FHMS 21-22 231 EGA

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

No IPD is planned

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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