AzTrials
AzTrials

MicronutrientsNCT04734938

The Effect on Micronutrient Status of a Diet of 100% Huel

A study testing Huel Powder in people with Micronutrients, run by Newcastle University 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
Search all trials

Trial summary

This project will assess the effect of Huel Food replacement on the micronutrient status of healthy volunteers over a 4-week period. To achieve this, 30 (non-smoking) generally healthy volunteers will be recruited to attend the study centre on three separate occasions. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Micronutrients
What is being tested?
Huel Powder
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited Kingdom
Study dates
19 Oct 2020to 28 Oct 2021
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

  • generally health (includes not having been diagnosed with any eating disorders and not receiving regular medication other than contraceptives or statins)
  • 18 years or older,
  • non-pregnant,
  • non-lactating
  • non-smoking,
  • no known food allergies.

Who cannot join

  • taking medication for long term illnesses such as high blood pressure, heart disease, or medication that affects liver or kidney function.

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Newcastle University

    Newcastle, Tyne and Wear, NE2 4HH

Other trials in United Kingdom

About this study

This project will assess the effect of Huel Food replacement on the micronutrient status of healthy volunteers over a 4-week period.

To achieve this, 30 (non-smoking) generally healthy volunteers will be recruited to attend the study centre on three separate occasions. Volunteers will be asked to consume their normal diet for one week whilst recording what they eat. They will then be asked to only consume Huel Powder and water for 4 weeks.

Read the detailed description

Study Protocol The effect on Micronutrient Status of a diet of 100% Huel

Aims of the study This project will assess the effect of Huel Powder on 30 generally healthy individuals over 4 weeks on the volunteer's micronutrient status. The aim is to identify any changes in the micronutrient status of volunteers in any of the 20 micronutrients to be monitored. Micronutrient status will be measured at the start of the study, after one week of their habitual diets and again after four weeks of consuming Huel powder as their single food source.

Huel Powder is a nutritionally complete powdered food that is high in protein and fibre, essential fats, carbohydrates, rich in phytonutrients and all 26 essential vitamins and minerals, with further information on Huel's website https://huel.com/pages/what-people-ask-about-huel.

Secondary measures of BMI, weight, waist and hip circumferences, and body composition will also be taken to observe any changes over the study period.

All researchers will be trained in GCP and phlebotomy. Potential volunteers will sent a health and activity questionnaire to assess their energy consumption and expenditure. This can be discussed over a Zoom call (or similar platform) if required. This will be used to screen the volunteers to see if they are suitable for the study. The energy intake information will also be verified from the first week of the study when they are consuming their habitual diet and completing their food diaries on my fitness pal. The energy requirements will inform the researcher how much Huel the volunteers will require over the course of the four weeks.

The volunteers will come to the study centre at Newcastle on three separate occasions. The first, at the start of the study they can have any further questions answered and if they are happy to take part in the study, they will be asked to complete a written consent form. They will also have their height, weight, body composition, waist and hip circumferences, measured as well as giving a blood sample (30ml) for micronutrient analysis. The second visit, at the end of the first week, will also measure the weight, body composition, waist circumference and take a blood sample. The final visit will be at the end of the study taking weight, body composition, waist circumference and a blood sample for micronutrient analysis.

The micronutrients and blood markers to be measure are listed below.

Markers to be tested; Haemoglobin Sodium Calcium HbA1c Cholesterol status Iron status Vitamin A Vitamin D Vitamin E Vitamin C Folate Vitamin B12 Choline Magnesium Potassium Zinc Copper Manganese Selenium Iodine (TSH)

Analysis Plan Although this trial is a pilot study, changes in BMI, weight, body composition, waist circumference, and micronutrient/blood marker will be compared between 0 and 1 week, as well as 1 week and 5 weeks, will be assessed. A one-way ANOVA will be used to assess differences for individual volunteers.

Test conditions Each volunteer will be asked to continue to consume their habitual diet for the first week and record their food intake in food diary app, myfitnesspal. At the end of the first week volunteers will be asked to consume only the Huel Powder provided and water. Volunteers will be asked not to consume any other food or drinks during these four weeks but still record their Huel intake in myfitnesspa.

  • 100% Huel - Only a diet comprising of Huel powder must be consumed for the last four weeks of the trial. No other snacks/food are permitted.
  • Energy intake - Daily calorie requirements varies from person to person and is determined by weight, height, gender, age and activity levels. The researchers will help estimate individual calorie requirements. Once you have your calorie requirements, manipulate your Huel serving sizes to reflect daily calorie intake.
  • Huel products - Only Huel powder - as well as Huel Flavour Boosts, if desired - must be consumed as part of this study. Huel Granola or Huel Bars cannot be consumed during this study.
  • Fluid intake - Only plain water, herbal tea (excluding citrus teas), black tea or coffee must be drunk. No additions must be made to fluid, i.e. no additional sugar, sweeteners, milk or honey are permitted during the length of the study.
  • Alcohol intake - No alcohol must be consumed during the study.
  • Exercise/Activity- Participants are able to continue with normal exercise and activity during the study.

Volunteers Thirty generally healthy volunteers, males and nonpregnant, nonlactating females aged over 18 years will be recruited for the study. Volunteers will be recruited by posters and word of mouth from Newcastle University staff and their associates.

Anonymity

Volunteers will be assigned a 'Participant Identification Number', which volunteers will use to complete questionnaires and researcher will use to label volunteers blood samples. Ony one documents will contain volunteers names and Participant Identification Number, and this will be destroyed after the final volunteer has completed the study or once the study has been concluded, which ever occurs first. Consent forms will not contain Participant Identification Numbers and will be kept for 12 months after the completion of the study.

Conditions
Micronutrients
Being tested
Huel Powder
Keywords
Micronutrients

What participants receive

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

  • Huel PowderDietary supplement

    Huel is made of an ultra-fine blend of sustainable ingredients. Oats, rice, peas, coconut, flaxseed, and our unique mix of vitamins and nutrients to provide you a meal with all the carbohydrates, protein, essential fats, fibre, and all the 26 essential vitamins and minerals your body needs to thrive. Volunteers will consume only Huel as their food source for the final four weeks of the study.

Study groups in NCT04734938
Study groupRoleWhat they receive
Habitual DietNo interventionAll volunteers will participate in this arm, continuing this habitual diet for 1 week
100% HuelExperimentalAll volunteers will participate in this arm of the study and consumer 100% Huel as their food for 4 weeks
Receives: Dietary Supplement: Huel Powder

What is being measured

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

  1. Change in level of calcium, cholesterol status, haemoglobin, magnesium, sodium, potassium in blood

    Change in the level of alcium, cholesterol status, haemoglobin, magnesium, sodium, potassium in blood (mmol/l)

    Measured: week 0 and week 1

  2. Change in level of calcium, cholesterol status, haemoglobin, magnesium, sodium, potassium in blood

    Change in the level of calcium, cholesterol status, haemoglobin, magnesium, sodium, potassium in blood (mmol/l)

    Measured: week 1 and week 5

  3. Change in level of HbA1c in blood

    Change in the level of HbA1c in blood (mmol/mol)

    Measured: week 0 and week 1

  4. Change in level of HbA1c in blood

    Change in the level of HbA1c in blood (mmol/mol)

    Measured: week 1 and week 5

  5. Change in level of choline, copper, Iron status, selenium, Vitamin A, Vitamin C, Vitamin E, Vitamin D and Zinc

    Change in the level of choline, copper, Iron status, selenium, Vitamin A, Vitamin C, Vitamin E, Vitamin D and Zinc in blood (micro mol/l)

    Measured: week 0 and week 1

  6. Change in level of choline, copper, Iron status, selenium, Vitamin A, Vitamin C, Vitamin E, Vitamin D and Zinc

    Change in the level of choline, copper, Iron status, selenium, Vitamin A, Vitamin C, Vitamin E, Vitamin D and Zinc in blood (micro mol/l)

    Measured: week 1 and week 5

  7. Change in level of manganese and Folate

    Change in the level of manganese and Folate in blood (nmol/l)

    Measured: week 0 and week 1

  8. Change in level of manganese and Folate

    Change in the level of manganese and Folate in blood (nmol/l)

    Measured: week 1 and week 5

  9. Change in level of Vitamin B12

    Change in the level of Vitamin B12 in blood (pmol/l)

    Measured: week 0 and week 1

  10. Change in level of Vitamin B12

    Change in the level of Vitamin B12 in blood (pmol/l)

    Measured: week 1 and week 5

  11. Change in level of Thyroid Stimulating Hormone (TSH)

    Change in the level of THS in blood (mU/l)

    Measured: week 0 and week 1

  12. Change in level of Thyroid Stimulating Hormone (TSH)

    Change in the level of THS in blood (mU/l)

    Measured: week 1 and week 5

Secondary outcomes (8)
  1. Change in BMI

    change in BMI (kg/m2)

    Measured: Week 0 and week 1

  2. Change in BMI

    change in BMI (kg/m2)

    Measured: week 1 and week 5

  3. Change in Weight

    change in weight (kg)

    Measured: Week 0 and week 1

  4. Change in Weight

    change in weight (kg)

    Measured: week 1 and week 5

  5. Change in hip to waist ratio

    change in hip to waist ratio

    Measured: Week 0 and week 1

  6. Change in hip to waist ratio

    change in hip to waist ratio

    Measured: week 1 and week 5

  7. Change in body composition of fat

    change in body composition of fat (%) as measured by impedance

    Measured: week 0 and week1

  8. Change in body composition of fat

    change in body composition of fat (%) as measured by impedance

    Measured: week 1 and week 5

Timeline

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

  1. First posted2 Feb 2021
  2. Study start19 Oct 2020
  3. Primary completion29 Jul 2021
  4. Study completion28 Oct 2021

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
Basic science
Allocation
Non-randomised
Intervention model
Crossover
Model description
Open label crossover trial
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04734938
Sponsor's protocol ID
2003/4657
Status last verified
Oct 2020
First submitted
8 Oct 2020
Last updated
13 May 2022
Results posted
No
Data monitoring committee
No
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 Huel Powder in people with Micronutrients, run by Newcastle University 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 1 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 13 May 2022. 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?

Change in level of calcium, cholesterol status, haemoglobin, magnesium, sodium, potassium in blood (time frame: week 0 and week 1). The study lists 12 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 13 May 2022.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in