- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06216626
PRebiotic Intervention for Metabolic and MEntal Health (PRIME) (PRIME)
Assessing the Effects of a Daily Prebiotic Fibre Blend on Inflammation, the Gut Microbiome, and Self-Report Measures of Mental Health in Individuals With Metabolic Syndrome
The purpose of the study is to determine whether a daily prebiotic fibre blend can reduce systemic inflammation, dyslipidemia, and self-report measures of mental health in individuals with metabolic syndrome. This study will help shape a larger randomised controlled study (RCT) powered to assess efficacy in a bigger cohort of patients.
Primary outcome measures will explore the efficacy of a prebiotic fibre blend on systemic inflammation. Secondary and exploratory outcomes measures will explore the efficacy of the prebiotic blend on clinical biomarkers associated with cardiometabolic risk factors, microbiota features, and mental health. Using these data, we will also estimate in-year savings for the NHS in the metabolic syndrome population on a per participant basis.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Metabolic syndrome is not a chronic disease, but a cluster of metabolic abnormalities including central obesity, insulin resistance, hyperglycemia, hypertension, and dyslipidemia. In the UK, it's estimated that 1 in 3 adults aged 50 years or over meets the criteria of metabolic syndrome. Emerging evidence suggests that metabolic syndrome is associated with low-grade systemic inflammation, which is thought to play a critical role in the subsequent pathogenesis of various metabolic and cardiovascular diseases. In fact, the inflammatory biomarker, high-sensitivity (hs)-CRP, has been shown to be predictive of whether metabolic syndrome progresses to a chronic disease, including cardiovascular disease (CVD), type 2 diabetes (T2D), and cancer mortality. Alongside metabolic disturbances, recent studies have shown that repeated (or long-term) exposure to systemic inflammation is also associated with an increased risk of future depressive and anxiety symptoms, potentially acting via the blood-brain barrier (BBB) interface.
From both a physical and mental health standpoint, it's clear that novel interventions, beyond pharmacotherapy, are needed to reverse the progression of metabolic syndrome, and reduce the risk of developing a long-term chronic disease, and poor mental health.
It is well established that dietary fibre plays a critical role in reducing symptoms of metabolic syndrome, including improvements in insulin sensitivity, glucose metabolism, lipid profile, and blood pressure. Specifically, dietary fibre has been shown to reduce cholesterol levels by binding to bile acids and promoting their excretion, as well as by decreasing the absorption of dietary cholesterol. Additionally, dietary fibre can slow the absorption of carbohydrates and reduce post-prandial glucose spikes, which may contribute to improvements in insulin sensitivity and metabolic health.
Growing evidence also suggests that the mechanisms underlying the benefits of fibre are thought to be mediated, at least in part, by the gut microbiota and their metabolites, such as short-chain fatty acids (SCFAs). A recent systematic review and meta-analysis of 10 randomised controlled trials found that increased intake of dietary fibre was associated with significant improvements in fasting glucose, insulin resistance, total cholesterol, and low-density lipoprotein (LDL) cholesterol levels in individuals with type 2 diabetes. Furthermore, a randomised controlled trial in individuals with metabolic syndrome found that supplementation with a prebiotic fibre blend led to significant reductions in fasting glucose, insulin resistance, and inflammatory markers. Therefore, increasing prebiotic fibre intake may represent a promising strategy for the prevention and management of metabolic symptoms, but remains poorly understood.
Prebiotics are specific types of fibres found in foods like onion, garlic, artichokes, asparagus, leeks, and chicory root. However, to reap the benefits of prebiotics for given health indications, this requires someone to consume roughly 5-10 onions a day. Prebiotic fibre blends (in powder form) are derived from a diversity of plant-based sources, and allows for the study of prebiotic-based benefits in a feasible, easy, measurable, and controlled way.
In this current study, we aim to assess the effects of a daily prebiotic fibre blend on systemic inflammation, the gut microbiome, lipid profiles, and self-report measures of mental health in individuals with metabolic syndrome. The study will be conducted over 12 weeks, and the findings may provide new insights into the potential role of prebiotics in the prevention and management of physical and mental health risk factors associated with chronic disease.
The study population will include adults aged 18-75 years who meet the criteria for metabolic syndrome. To promote the inclusion and diversity of participants across England, this study will be conducted remotely, by posting participants the at-home collection kits (stool and finger prick tests) and online surveys. This gives access to participants who would otherwise not be able to take part in research.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
London, United Kingdom, EC1N 2SW
- Myota Health
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Individuals aged 18-75 years with a diagnosis of Metabolic Syndrome (MetS), yet not receiving treatment for their symptoms
- MetS is diagnosed using the IDF criteria (Alberti, Zimmet & Shaw, 2006). MetS is defined as having abdominal obesity (waist circumference ≥ 94 cm in men, and ≥ 80 cm in women) plus two or more of the following: raised triglycerides (≥1.7 mmol/L); reduced HDL-C (< 1.03 mmol/L in men and < 1.29 mmol/L in women); raised systolic blood pressure (≥ 130 mmHg); raised diastolic blood pressure (≥ 85 mmHg); treatment of previously diagnosed hypertension; raised fasting plasma glucose (≥ 5.6 mmol/L); or previously diagnosed with pre-diabetes.
- Capacity to give informed consent
- Ability to comply with study requirements.
Exclusion Criteria:
- Includes a current diagnosis of Type 1 or 2 diabetes or cardiovascular disease
- receiving medications that lower cholesterol, blood pressure, or blood glucose levels
- pregnancy, lactation, or an intent to become pregnant during the course of the study
- continuous antibiotic use for > 3 days within 1 month prior to enrolment
- continuous use of weight-loss drug for > 1 month before screening
- major change in dietary intake in past month (e.g. excluding whole food groups)
- currently consuming large doses of prebiotic or probiotic supplements
- prior use (< 6 months) of any blood glucose or cholesterol lowering medication
- a significant gastrointestinal (GI) condition affecting absorption including (but not limited to) inflammatory bowel disease; weight loss surgery
- irritable bowel disease
- end stage renal disease
- active cancer, or treatment for any cancer, in last 3 years.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Prebiotic fibre
The treatment group will consume 10g per day of a diverse prebiotic fibre supplement.
Supplements are powdered and unflavoured, and given to the participants in 300g packets lasting for 30 days.
A 10g scoop is included in each packet and participants are advised to consume one level scoop at any time of the day.
Participants are provided with examples on how to consume the supplement (e.g., breakfast cereal, coffee, tea, water).
|
Each 10g daily serve of supplement contains the following fibres:
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Active Comparator: Control
Participants are provided with standard of care (dietary advice).
Recommendations for diet and lifestyle advice are provided by a UK-registered GP, and follow the Heart UK's Healthy Eating Guidelines.
These recommendations emphasise a Mediterranean diet, rich in fruit, vegetables, and healthy fats (omega-3 fatty acids), while reducing refined sugar, salt, processed foods, and alcohol intake.
The Mediterranean diet is considered a gold-standard for participants with MetS and poor mental health.
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Each 10g daily serve of supplement contains the following fibres:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
C-Reactive Protein
Time Frame: Baseline and Week 12
|
To compare the effect of Myota's prebiotic fibre blend versus standard of care on C-Reactive Protein levels
|
Baseline and Week 12
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gut Microbiome Profiles
Time Frame: Baseline and Week 12
|
To compare the effect of Myota's prebiotic fibre blend versus standard of care on gut microbiome profiles
|
Baseline and Week 12
|
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Lipid Profiles
Time Frame: Baseline and Week 12
|
To compare the effect of Myota's prebiotic fibre blend versus standard of care on lipid profiles
|
Baseline and Week 12
|
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Depression, Anxiety and Stress Scale (42-item)
Time Frame: Baseline and Week 12
|
To compare the effect of Myota's prebiotic fibre blend versus standard of care on Depression, Anxiety and Stress Scale (42-item) scores.
Minimum score = 0, maximum score = 126, where higher scores indicate worse outcomes.
|
Baseline and Week 12
|
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Patient Health Questionnaire (PHQ)
Time Frame: Baseline and Week 12
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To compare the effect of Myota's prebiotic fibre blend versus standard of care on Patient Health Questionnaire scores.
Minimum score = 1, maximum score = 27, where higher scores indicate worse outcomes.
|
Baseline and Week 12
|
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Perceived Stress Scale (PSS)
Time Frame: Baseline and Week 12
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To compare the effect of Myota's prebiotic fibre blend versus standard of care on Perceived Stress Scale scores.
Minimum score = 0, maximum score = 40, where higher scores indicate worse outcomes.
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Baseline and Week 12
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Generalised Anxiety Disorder (GAD) Scale
Time Frame: Baseline and Week 12
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To compare the effect of Myota's prebiotic fibre blend versus standard of care on Generalised Anxiety Disorder Scale scores.
Minimum score = 0, maximum score = 21, where higher scores indicate worse outcomes.
|
Baseline and Week 12
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Gastrointestinal Symptom Rating Scale (GSRS)
Time Frame: Baseline and Week 12
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To compare the effect of Myota's prebiotic fibre blend versus standard of care on Gastrointestinal Symptom Rating Scale scores.
Scores are calculated for 5 sub-categories: reflux, pain, constipation, diarrhoea, indigestion, where the minimum score is 1 and maximum score is 21, where higher scores indicate worse outcomes.
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Baseline and Week 12
|
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Diastolic blood pressure
Time Frame: Baseline and Week 12
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To compare the effect of Myota's prebiotic fibre blend versus standard of care on diastolic blood pressure.
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Baseline and Week 12
|
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Systolic Blood pressure
Time Frame: Baseline and Week 12
|
To compare the effect of Myota's prebiotic fibre blend versus standard of care on systolic blood pressure.
|
Baseline and Week 12
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dietary fibre intake
Time Frame: Baseline and Week 12
|
Assess the difference in dietary fibre intake as a confounding variable.
|
Baseline and Week 12
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Caitlin V Hall, PhD, Myota Health
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PRIME
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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