- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03315988
The Effects of an 8-week Vegan Diet on TMAO Levels and Post-challenge Glucose Levels in Individuals With Dysglycaemia (PYH)
The Effects of an 8-week Vegan Diet on Trimethylamine-N-Oxide (TMAO) Levels and Post-challenge Glucose Levels in Individuals With Dysglycaemia (The Plant Your Health Study)
The amount of people with diabetes mellitus has now reached over 4 million in the United Kingdom. Type 2 diabetes accounts for the majority of all cases of diabetes and increases the risk of many other diseases such as heart problems. Plant based diets are thought to be an effective way to improve markers of health related to type 2 diabetes and heart disease. One way that a plant based diet improves health could be through reducing waste products that are generated in the gut by the bacteria that break down food as part of the digestion process. For example, the digestion of some meats, fish and eggs results in the creation of a substance called Trimethylamine-N-Oxide (TMAO) which has been linked to worse health outcomes in several studies. However, the full impact on TMAO and blood glucose levels of swapping regular meat consumption for a plant based vegan diet is not fully understood and requires further research. Therefore, the aim of this study will be to develop and undertake a clinical trial to investigate the effects of an 8-week vegan diet on TMAO levels and post challenge glucose levels in individuals with dysglycaemia (drug naïve).
The study will be interventional single group prospective trial of adults aged 18-75 years of age from a multi-ethnic population with dysglycaemia (drug naïve). A sample of 29 people will be sought. The dietary intervention (vegan diet) will last 8 weeks. Then, the participants will go back to their normal diet and come for their final visit after a four week follow-up period (week 12). To assess the effectiveness of the intervention, primary and secondary outcome data collected at baseline will be compared with data collected at 1 week, 8 weeks and 12 weeks.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Design
Interventional single group prospective trial in a patient population with identified dysglycaemia within the past 36 months defined as 2h post-challenge glucose ≥7.8 mmol/L after a standard oral glucose tolerance test or HbA1c ≥5.7% (39-46 mmol/mol). This phase clinical trial will evaluate the efficacy and underlining mechanisms of a vegan diet in promoting cardiometabolic health in those with dysglycaemia. Specifically, this trial will aim to investigate the effect of an 8-week vegan diet with follow-up at 1, 8 and 12 weeks.
Study Setting
The study will be co-ordinated within the Leicester Biomedical Research Centre (Leicester Diabetes Centre) at the Leicester General Hospital. Clinical measurement sessions will be carried out by the appointed research team. Participants will be asked to visit the study centre on five occasions.
Intervention Description and Definition
The participants will be asked to follow a diet that excludes foods hypothesised to support the syntheses of TMAO, particularly meat (any), eggs and fish (any). A number of studies suggest that dairy products may also have an effect in modulating TMAO production whereas other studies do not. Therefore, in order to avoid any potential contaminating or confounding effect, dairy products will also be avoided.
The diet employed in this study is broadly aligned to a vegan diet. The term vegan will be used to aid behaviour change and food choice. For example, an increasing array of products are now pack marked as vegan. The participants will be asked to keep their diet similar to their original and the Registered Dietitian involved in this study will plan their weekly menus accordingly.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Leicester, United Kingdom, LE3 4PW
- Leicester Diabetes Centre
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Participant is willing and able to give informed consent for participation in the study
And either:
- Overweight (White: BMI>25 - <30, South Asian/ Black and minority ethnic group <27.5) with HbA1c between HbA1c ≥5.7% and ≤ 8% (39-64 mmol/mol) identified within the last 36 months
- Obese: (White: BMI ≥30, South Asian/ Black and minority ethnic group: ≥27.5)
- Male or Female
- Aged 18 - 75 years inclusive
- Able to understand, read and speak the English language to a sufficient level to understand and take part to the study in the investigators opinion
- Have access to a phone, and willing to use it as part of the study
- Regular meat and/or fish eater (at least 3 times per week)-self reported
Exclusion Criteria:
Participant is unwilling or unable to give informed consent
- Non-English speakers
- HbA1c above 8% (64 mmol/mol)
- Taking any form of glucose lowering medication currently or within the last 60 days
- Current smokers
- Current use of vegan or vegetarian diet
- Recent significant weight change (10% or more) over the last 3 months
- Pregnancy/lactation
- Clinical eating disorder as detected by their GP or relevant health professional (e.g. dietitian)
- Have a terminal illness
- Current or recent (within 6 months) oral antibiotics or steroid use as their usage could impact on the gut bacteria profile
Ongoing CVD (e.g. angina) *
- In the circumstance that an individual is not sure whether they meet the inclusion/ exclusion criteria, (i.e. they are not sure if they have ongoing CVD) this will be reviewed by a named medic on the delegation of authority log for a clinical decision to be made during baseline.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Vegan diet
Intervention Description and Definition The participants will be asked to follow a diet that excludes foods hypothesised to support the syntheses of TMAO, particularly meat (any), eggs and fish (any). A number of studies suggest that dairy products may also have an effect in modulating TMAO production whereas other studies do not. Therefore, in order to avoid any potential contaminating or confounding effect, dairy products will also be avoided. The diet employed in this study is broadly aligned to a vegan diet. The term vegan will be used to aid behaviour change and food choice. For example, an increasing array of products are now pack marked as vegan. The participants will be asked to keep their diet similar to their original and the Registered Dietitian involved in this study will plan their weekly menus accordingly. |
Adoption of a vegan diet The participants of this study wil be asked to adopt a vegan diet under the supervision of a Registered Dietitian.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline TMAO plasma levels at 1, 8 and 12 weeks.
Time Frame: at 1 (+ 5 days) week , 8 (+/- 5 days) weeks and 12 weeks (+/- 5 days)
|
urine and plasma samples for TMAO (μM)
|
at 1 (+ 5 days) week , 8 (+/- 5 days) weeks and 12 weeks (+/- 5 days)
|
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Change from Baseline 3-hour post-challenge glucose levels at 1, 8 and 12 weeks.
Time Frame: at 1 (+ 5 days) week , 8 (+/- 5 days) weeks and 12 weeks (+/- 5 days)
|
blood samples (mmol/l)
|
at 1 (+ 5 days) week , 8 (+/- 5 days) weeks and 12 weeks (+/- 5 days)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
TMAO (μM) urine levels at baseline.
Time Frame: at baseline
|
urine samples
|
at baseline
|
|
Change from Baseline in TMAO urine/plasma levels at 1 week following a vegan diet.
Time Frame: at 1 week (+ 5 days)
|
urine and plasma samples; TMAO (μM)
|
at 1 week (+ 5 days)
|
|
Change from Baseline 3-hour post-challenge glucose levels at 1 week following a vegan diet.
Time Frame: at 1 week (+ 5 days)
|
blood samples for glucose (mmol/l)
|
at 1 week (+ 5 days)
|
|
Change from week 8 in TMAO urine/plasma levels at 4 weeks after diet has returned to normal (week 12).
Time Frame: at 12 weeks (+/- 5 days)
|
urine and plasma samples for TMAO (μM)
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at 12 weeks (+/- 5 days)
|
|
Change from week 8 in 3-hour post-challenge glucose levels at 4 weeks after diet has returned to normal (week 12).
Time Frame: at 12 weeks (+/- 5 days)
|
blood samples for glucose (mmol/l)
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at 12 weeks (+/- 5 days)
|
|
Change from Baseline in body composition using dual energy X-ray absorptiometry (DXA) scan at 8 weeks following a vegan diet.
Time Frame: at baseline and week 8 (+/- 5 days)
|
DXA Scan
|
at baseline and week 8 (+/- 5 days)
|
|
Change from Baseline in biochemical measures of cardiometabolic health including post-challenge insulin at 1 week.
Time Frame: 1 week (+5 days)
|
blood samples (mmol/l)
|
1 week (+5 days)
|
|
Change from Baseline in biochemical measures of cardiometabolic health including post-challenge insulin at 8 weeks.
Time Frame: 8 weeks (+/- 5 days)
|
blood samples (mmol/l)
|
8 weeks (+/- 5 days)
|
|
Change from Baseline in biochemical measures of cardiometabolic health including post-challenge insulin at 12 weeks.
Time Frame: 12 weeks (+/- 5 days)
|
blood samples (mmol/l)
|
12 weeks (+/- 5 days)
|
|
Change from Baseline in biochemical measures of cardiometabolic health including fasting lipids and at 1 week.
Time Frame: 1 week (+5 days)
|
blood samples (mmol/l)
|
1 week (+5 days)
|
|
Change from Baseline in biochemical measures of cardiometabolic health including fasting lipids and inflammatory markers at 8 weeks.
Time Frame: 8 weeks (+/- 5 days)
|
blood samples (mmol/l)
|
8 weeks (+/- 5 days)
|
|
Change from Baseline in biochemical measures of cardiometabolic health including fasting lipids at 12 weeks.
Time Frame: 12 weeks (+/- 5 days)
|
blood samples (mmol/l)
|
12 weeks (+/- 5 days)
|
|
Change from Baseline in biochemical measures of cardiometabolic health including inflammatory markers at 1 week.
Time Frame: 1 week (+5 days)
|
blood samples (mmol/l)
|
1 week (+5 days)
|
|
Change from Baseline in biochemical measures of cardiometabolic health including inflammatory markers at 8 weeks.
Time Frame: 8 weeks (+/- 5 days)
|
blood samples (mmol/l)
|
8 weeks (+/- 5 days)
|
|
Change from Baseline in biochemical measures of cardiometabolic health including inflammatory markers at 12 weeks.
Time Frame: 12 weeks (+/- 5 days)
|
blood samples (mmol/l)
|
12 weeks (+/- 5 days)
|
|
The extent to which changes in the primary outcomes are mediated by, or independent of, changes to body composition.
Time Frame: baseline
|
DXA scan
|
baseline
|
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The extent to which changes in the primary outcomes are mediated by, or independent of, changes to body composition.
Time Frame: week 8 (+/- 5 days)
|
DXA scan
|
week 8 (+/- 5 days)
|
|
The extent to which changes in the primary outcomes are mediated by, or independent of, changes to lifestyle factors.
Time Frame: baseline
|
3-day diet diaries
|
baseline
|
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The extent to which changes in the primary outcomes are mediated by, or independent of, changes to lifestyle factors.
Time Frame: counselling visit (+5 days)
|
3-day diet diaries
|
counselling visit (+5 days)
|
|
The extent to which changes in the primary outcomes are mediated by, or independent of, changes to lifestyle factors.
Time Frame: week 1 (+5 days)
|
3-day diet diaries
|
week 1 (+5 days)
|
|
The extent to which changes in the primary outcomes are mediated by, or independent of, changes to lifestyle factors.
Time Frame: week 8 (+/- 5 days)
|
3-day diet diaries
|
week 8 (+/- 5 days)
|
|
The extent to which changes in the primary outcomes are mediated by, or independent of, changes to lifestyle factors.
Time Frame: week 12 (+/- 5 days)
|
3-day diet diaries
|
week 12 (+/- 5 days)
|
|
The extent to which changes in the primary outcomes are mediated by, or independent of, changes to lifestyle factors.
Time Frame: weeks 1-12
|
accelerometers
|
weeks 1-12
|
|
Semi-structured interviews with the completers, at the end of the study, to investigate perception responses having been on a vegan diet.
Time Frame: at week 12 (+/- 5 days)
|
semi-structured interviews
|
at week 12 (+/- 5 days)
|
Collaborators and Investigators
Sponsor
Collaborators
Publications and helpful links
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0625
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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