- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04719429
The Effects of Cricket- and Beef-derived Protein on Plasma Amino Acid Concentrations and Appetite Responses
The Effects of Dietary Protein Source on Postprandial Plasma Amino Acid Availability, Gut-derived Appetite Regulating Hormones, and Subjective Appetite Sensations in Young Males
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
With the rapid increase in the global population, the production of sufficient amounts of conventional animal-based protein to meet global dietary demands may no longer be desired nor feasible. Insects may represent an environmentally sustainable additional source of dietary protein that has the potential to help ensure global food security in the future. However, the functional characteristics of insect-derived proteins when fed to humans is unclear. Further, how insect-derived proteins compare to other animal-derived proteins (e.g. from beef) have not been explored.
The purpose of this study was to compare postprandial plasma glucose, insulin, and amino acid concentrations, gut-derived appetite regulatory hormones, subjective appetite sensations, and ad libitum energy intake following the ingestion of 25 g insect- or beef-derived protein in healthy young men. It was hypothesized that hyperaminoacidaemia would be more rapid following the ingestion of beef-derived protein compared to cricket-derived protein, although total amino acid availability would be similar between protein sources over a 300-minute postprandial period. It was further hypothesized there would be no difference between protein sources on postprandial subjective appetite sensations or subsequent ad libitum energy intake.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Quebec
-
Montreal, Quebec, Canada, H2W 1S4
- Exercise Metabolism and Nutrition Research Laboratory
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Male
- Aged between 18-35 years inclusive
- Healthy, moderately active
- BMI < 30 kg/m2 and > 18.5 kg/m2
- Having given informed consent
Exclusion Criteria:
- Presence of any identified metabolic or intestinal disorders
- Use of tobacco products
- Adherence to a strict vegetarian or vegan diet
- Use of medications known to affect protein metabolism
- Allergy to shellfish or crustaceans
- Allergy to beef protein
- Engagement in physical exercise training more than 6 days per week
Study Plan
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: QUADRUPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Cricket-derived protein beverage
Ingestion of a cricket-derived protein beverage
|
Beverage containing 25 g cricket-derived protein
|
|
EXPERIMENTAL: Beef-derived protein beverage
Ingestion of a beef-derived protein beverage
|
Beverage containing 25 g beef-derived protein
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Plasma leucine concentration
Time Frame: 0-5 hours in the post-prandial period
|
umol/L
|
0-5 hours in the post-prandial period
|
|
Subjective appetite sensations (hunger, fullness, desire to eat, prospective food consumption)
Time Frame: 0-5 hours in the post-prandial period
|
mm (visual analogue scale)
|
0-5 hours in the post-prandial period
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Plasma branched-chain amino acid concentration
Time Frame: 0-5 hours in the post-prandial period
|
umol/L
|
0-5 hours in the post-prandial period
|
|
Plasma essential amino acid concentration
Time Frame: 0-5 hours in the post-prandial period
|
umol/L
|
0-5 hours in the post-prandial period
|
|
Plasma non-essential amino acid concentration
Time Frame: 0-5 hours in the post-prandial period
|
umol/L
|
0-5 hours in the post-prandial period
|
|
Plasma total amino acid concentration
Time Frame: 0-5 hours in the post-prandial period
|
umol/L
|
0-5 hours in the post-prandial period
|
|
Plasma glucose
Time Frame: 0-5 hours in the post-prandial period
|
mmol/L
|
0-5 hours in the post-prandial period
|
|
Plasma insulin
Time Frame: 0-5 hours in the post-prandial period
|
pmol/L
|
0-5 hours in the post-prandial period
|
|
Plasma GLP-1
Time Frame: 0-5 hours in the post-prandial period
|
pg/mL
|
0-5 hours in the post-prandial period
|
|
Plasma PYY
Time Frame: 0-5 hours in the post-prandial period
|
pg/mL
|
0-5 hours in the post-prandial period
|
|
Ad libitum food energy intake
Time Frame: assessed 5 hours after protein intake
|
kJ
|
assessed 5 hours after protein intake
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- A08-M28-18B
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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