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Cricket ProteinCriProBNCT06906159

Cricket Protein Bioavailability in Younger, Middle-Aged and Older Adults

A study testing Cricket protein and Whey protein in people with Cricket Protein and Whey Protein, run by University of Surrey at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

A global shift towards sustainable food sources is now emerging, largely due to the immense environmental pressure that comes from producing animal foods, particularly beef. Insects present a novel source of sustainable dietary protein due to their high protein content. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Cricket Protein, Whey Protein
What is being tested?
Cricket protein and Whey protein
Could I receive a placebo?
No, everyone receives an active treatment
How many people
45 participants
Where
1 siteUnited Kingdom
Study dates
11 Mar 2024to 10 Mar 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Healthy adult males and females in general good health, aged between 18 - 35 years, 40 - 55 years or over 65 years
  • BMI between 18.5 and 35 kg/m2
  • Stable weight for at least 3 months
  • Volunteers must be able and willing to give informed written consent
  • Volunteers must be able to eat egg
  • Volunteers must be willing to provide blood samples

Who cannot join

  • Current or previous gastrointestinal conditions (e.g. Crohn's disease, Coeliac disease, Irritable Bowel Syndrome) - assessed via a health questionnaire
  • Those with diabetes or other metabolic conditions - assessed via a health questionnaire
  • Those taking food supplements which may impact digestion (e.g., digestive enzymes, probiotics, fibre supplements)
  • Those smoking, using nicotine products (e.g., e-cigarettes, patches) or not abstained from these activities for more than 6 months - assessed via a health questionnaire
  • Pregnant or lactating
  • Volunteers with a high daily caffeine intake > 300 mg/day (more than 5 cups of standard coffee per day)
Show all 10Show fewer
  • Drug or alcohol abuse in the last 2 years
  • Those who are currently taking part in a clinical trial or another research study or have taken part within the last 3 months
  • Those with food allergies, dietary intolerance or Coeliac disease - assessed via a health questionnaire
  • Those following weight loss diets

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • University of Surrey

    Guildford, Surrey, GU2 7XH

Other trials in United Kingdom

About this study

Official title: Cricket Protein Bioavailability in Younger, Middle-Aged and Alder Adults

A global shift towards sustainable food sources is now emerging, largely due to the immense environmental pressure that comes from producing animal foods, particularly beef. Insects present a novel source of sustainable dietary protein due to their high protein content. This is particularly relevant for older adults, as protein becomes increasingly more important in later life. It helps to maintain muscle as we age, which is crucial for reducing frailty, falls and early mortality. We want to find out more about the digestion and absorption of insect protein in older people to see if it could be a beneficial source of protein to help maintain muscle. We are interested in the use of insect-based solid foods, especially the use of flour made from grounded whole crickets. We want to explore the digestibility of cricket protein compared to a commonly used animal alternative (whey protein) to find out if it can be efficiently absorbed and utilised within humans.

Read the detailed description

Participants are asked to fast overnight and come in the following day for one of two visits where they are given a standardised breakfast muffin containing either cricket protein or whey protein (250-300 kcal; approx. 12% fat, 45% carbohydrates including 10% sugars, 35% protein, 0.4% salt and 6% fibre) after which they breathe into a test tube in 15-30 minute intervals for 4 hours. In addition to this, we collect a blood sample (10ml) every 15 minutes for the first hour and then every 30 minutes for the next 3 hours (110ml of blood in total per visit) so we can determine changes in blood amino acids, glucose and fat concentrations after eating the muffin. In total we only collect a small amount of blood. This method of blood collection is the same method used for a traditional blood test but to avoid repeated needle insertions we use a cannula which remains in the participant's arm for the duration of the visit so that only a single needle insertion is necessary.

The muffin contains a small amount of a natural fat called octanoic acid. The octanoic acid is enriched with carbon-13. This is a natural variant of carbon and is safe to use, even in babies and pregnant women. At the end of each test visit we ask participants to fill out a short questionnaire to ask about the taste of the muffins. Participants are required to repeat this whole process for a second visit in which they consume the other muffin.

The muffins are identical between the two test visits with the exception that one muffin is made with a milk-based protein (whey) whereas the other test muffin is made with an insect protein (cricket). The test muffins are similar in size, shape, and taste. Participants are randomised to a muffin condition in a crossover design. Participants are blinded to the muffin condition and only one member of the research team knows which muffin participants receive on which test visit but they are not present during the test visits. The researchers conducting the test visits do not know which muffin is being consumed by participants.

Participants are required to attend for 2 test visits each lasting approximately 5 hours. This takes place in the Clinical Investigation Unit (CIU) at the University of Surrey. On the day before each of the test visits participants are asked to arrive fasted for 12 hours overnight, refrain from strenuous exercise, alcohol, caffeine and food containing corn, broccoli, sugarcane, and tropical fruits (because of the type of natural carbon-13 they contain) the day before their visits.

Being tested
Cricket protein, Whey protein

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Cricket proteinDietary supplement

    Muffins made with cricket-derived protein from house crickets (Acheta domesticus )

  • Whey proteinDietary supplement

    Muffins made with whey protein

Study groups in NCT06906159
Study groupRoleWhat they receive
Cricket muffinExperimentalMuffin made with cricket-derived protein powder
Receives: Dietary Supplement: Cricket protein
Whey muffinActive comparatorMuffin made with whey protein powder
Receives: Dietary Supplement: Whey protein

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Gastric emptying

    Exhaled breath is used to assess the rate of gastric emptying of the protein muffins

    Measured: 4 hour post-prandial period

  2. Plasma amino acids

    Blood samples are used to assess the plasma amino acid response to consuming the protein muffins

    Measured: 4 hour post-prandial period

Secondary outcomes (1)
  1. Metabolic markers

    Blood samples are also used to assess post-prandial glucose, triglycerides and cholesterol

    Measured: 4 hour post-prandial period

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Apr 2025
  2. Study start11 Mar 2024
  3. Primary completion10 Mar 2025
  4. Study completion10 Mar 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Crossover
Model description
Repeated measures randomised crossover design
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
45 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06906159
Sponsor's protocol ID
CriProB
Acronym
CriProB
Status last verified
Mar 2025
First submitted
8 Jan 2025
Last updated
2 Apr 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Cricket protein and Whey protein in people with Cricket Protein and Whey Protein, run by University of Surrey at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Gastric emptying (time frame: 4 hour post-prandial period). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Apr 2025.

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