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.
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
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 group | Role | What they receive |
|---|---|---|
| Habitual Diet | No intervention | All volunteers will participate in this arm, continuing this habitual diet for 1 week |
| 100% Huel | Experimental | All 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.
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
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
Change in level of HbA1c in blood
Change in the level of HbA1c in blood (mmol/mol)
Measured: week 0 and week 1
Change in level of HbA1c in blood
Change in the level of HbA1c in blood (mmol/mol)
Measured: week 1 and week 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
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
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
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
Change in level of Vitamin B12
Change in the level of Vitamin B12 in blood (pmol/l)
Measured: week 0 and week 1
Change in level of Vitamin B12
Change in the level of Vitamin B12 in blood (pmol/l)
Measured: week 1 and week 5
Change in level of Thyroid Stimulating Hormone (TSH)
Change in the level of THS in blood (mU/l)
Measured: week 0 and week 1
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)
Change in BMI
change in BMI (kg/m2)
Measured: Week 0 and week 1
Change in BMI
change in BMI (kg/m2)
Measured: week 1 and week 5
Change in Weight
change in weight (kg)
Measured: Week 0 and week 1
Change in Weight
change in weight (kg)
Measured: week 1 and week 5
Change in hip to waist ratio
change in hip to waist ratio
Measured: Week 0 and week 1
Change in hip to waist ratio
change in hip to waist ratio
Measured: week 1 and week 5
Change in body composition of fat
change in body composition of fat (%) as measured by impedance
Measured: week 0 and week1
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.
- First posted2 Feb 2021
- Study start19 Oct 2020
- Primary completion29 Jul 2021
- Study completion28 Oct 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for MicronutrientsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Newcastle University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Jeffrey Pearson, PhD, Principal investigator, Newcastle University
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
Study at a glance
From the registry record, last updated by the sponsor on 13 May 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect on Micronutrient Status of a Diet of 100% Huel
- ClinicalTrials.gov ID
- NCT04734938
- Acronym / sponsor ID
- 2003/4657
- Conditions
- Micronutrients
- Keywords
- Micronutrients
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- Newcastle UniversityUniversity, hospital or other
- Study start
- 19 Oct 2020 (actual)
- Primary completion
- 29 Jul 2021 (actual)
- Study completion
- 28 Oct 2021 (actual)
- First posted
- 2 Feb 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Basic science
- Allocation
- Non-randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Open label crossover trial
| Arm | Type | Receives |
|---|---|---|
| Habitual Diet | No intervention | –All volunteers will participate in this arm, continuing this habitual diet for 1 week |
| 100% Huel | Experimental | Dietary Supplement: Huel PowderAll volunteers will participate in this arm of the study and consumer 100% Huel as their food for 4 weeks |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- 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,
Key exclusion criteria (1 listed)
- taking medication for long term illnesses such as high blood pressure, heart disease, or medication that affects liver or kidney function.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Huel PowderHuel 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. | Dietary supplement | 100% Huel |
Primary outcome
Change in level of calcium, cholesterol status, haemoglobin, magnesium, sodium, potassium in blood
Time frame: week 0 and week 1
Change in the level of alcium, cholesterol status, haemoglobin, magnesium, sodium, potassium in blood (mmol/l)
Change in level of calcium, cholesterol status, haemoglobin, magnesium, sodium, potassium in blood
Time frame: week 1 and week 5
Change in the level of calcium, cholesterol status, haemoglobin, magnesium, sodium, potassium in blood (mmol/l)
Change in level of HbA1c in blood
Time frame: week 0 and week 1
Change in the level of HbA1c in blood (mmol/mol)
Change in level of HbA1c in blood
Time frame: week 1 and week 5
Change in the level of HbA1c in blood (mmol/mol)
Change in level of choline, copper, Iron status, selenium, Vitamin A, Vitamin C, Vitamin E, Vitamin D and Zinc
Time frame: week 0 and week 1
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)
Change in level of choline, copper, Iron status, selenium, Vitamin A, Vitamin C, Vitamin E, Vitamin D and Zinc
Time frame: week 1 and week 5
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)
Change in level of manganese and Folate
Time frame: week 0 and week 1
Change in the level of manganese and Folate in blood (nmol/l)
Change in level of manganese and Folate
Time frame: week 1 and week 5
Change in the level of manganese and Folate in blood (nmol/l)
Change in level of Vitamin B12
Time frame: week 0 and week 1
Change in the level of Vitamin B12 in blood (pmol/l)
Change in level of Vitamin B12
Time frame: week 1 and week 5
Change in the level of Vitamin B12 in blood (pmol/l)
Change in level of Thyroid Stimulating Hormone (TSH)
Time frame: week 0 and week 1
Change in the level of THS in blood (mU/l)
Change in level of Thyroid Stimulating Hormone (TSH)
Time frame: week 1 and week 5
Change in the level of THS in blood (mU/l)
8 secondary outcomes
Change in BMI
Time frame: Week 0 and week 1
Change in BMI
Time frame: week 1 and week 5
Change in Weight
Time frame: Week 0 and week 1
Change in Weight
Time frame: week 1 and week 5
Change in hip to waist ratio
Time frame: Week 0 and week 1
Change in hip to waist ratio
Time frame: week 1 and week 5
Change in body composition of fat
Time frame: week 0 and week1
Change in body composition of fat
Time frame: week 1 and week 5
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 May 2022.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Jeffrey Pearson, PhD principal investigator
Newcastle University
1 site in 1 country: see every site and its status.
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.