- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01114399
Diet and Vascular Health Study (BROCCOLI)
July 28, 2014 updated by: Quadram Institute Bioscience
The aim of this study is to examine the effects of a diet rich in broccoli on cardiovascular disease risk using biochemical indicators such as blood lipid profiles, most notably cholesterol; markers of inflammation as well as established physiological measurements such as Pulse wave velocity (PWV), Augmentation index (AIx) and Ambulatory Blood Pressure Measurements (ABPM).
Broccoli contains compounds known as glucosinolates which are metabolised to isothiocyanates when consumed.
The major glucosinolate in broccoli is known as glucoraphanin which produces the isothiocyanate sulforaphane.
The glucosinolates are thought to be the principal component in broccoli that may reduce CVD risk.
The investigators will use a standard cultivar of broccoli and a cultivar that has enhanced levels of glucosinolates ('HG broccoli').
This broccoli has been used in previous intervention studies (e.g.
ClinicalTrials.gov
NCT00535977).
Volunteers will be asked to consume 400g of standard broccoli, HG broccoli or peas each week over a 12 week period in a double blinded (for the broccoli) parallel study.
The volunteers recruited will, according to the Joint British Societies (JBS 2) Guidelines on the prevention of cardiovascular disease (CVD) in clinical practise, have a 10-20% (mild to moderate) risk of developing cardiovascular disease or having a cardiovascular (CV) event in the next 10 years.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
48
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Norfolk
-
Norwich, Norfolk, United Kingdom, NR4 7UA
- Institute of Food Research
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
50 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Men and women aged ≥ 50 years will be recruited onto the study using the JBS 2 cardiac risk assessor calculator (Copyright University of Manchester 1998): Scores of 10-20% will be acceptable for participation in the study.
- Total cholesterol ≥ 5.0mmol/L
Blood pressure measurements
- Systolic≥ 120mmHg
- Diastolic ≥ 80mmHg
- BMI ≥20
- Smokers and Non Smokers
Exclusion Criteria:
- Diagnosed diabetics;
- Fasting glucose >6mmol/L;
- Blood pressure <90/50 or 95/55 if symptomatic; >160/100
- Chronic kidney disease;
- Those on any lipid lowering therapies like statins, bile acid sequestrants, cholesterol absorption inhibitors and nicotinic acid;
- Those who have suffered a cardiovascular event like stroke, myocardial infarction or trans ischemic attacks;
- Peripheral vascular disease including Claudication
- Consumption of fish oil supplements (unless volunteer is willing to discontinue their use 4 weeks prior to the start of the)
- Parallel participation in another research project which involves dietary intervention and/or sampling of biological fluids/materials
- Any person related or living with any member of the study team
- Participation in another research project which involves blood sampling within the last four months; Blood from both studies should not exceed 470mL
- BMI <20
- BMI >40
- Fasting total cholesterol > 8.0mmol/L
- Gastrointestinal disease (excluding hiatus hernia) unless symptomatic or study intervention/procedure is contraindicated
- Going on holiday for more than 7 days in any single period or within 2 weeks of their clinical appointment at the CRTU
- Currently suffering from or have suffered from any neck and throat injuries and surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Standard Broccoli
|
One group will consume 400g of standard broccoli each week for 12weeks; the second group will consume 400g of the high glucosinolate broccoli each week for 12weeks while the third group will consume 400g of peas each week for 12weeks.
The broccoli and the peas will be consumed on top of the volunteer's standard diet.
|
|
Experimental: High Glucosinolate Broccoli
|
One group will consume 400g of standard broccoli each week for 12weeks; the second group will consume 400g of the high glucosinolate broccoli each week for 12weeks while the third group will consume 400g of peas each week for 12weeks.
The broccoli and the peas will be consumed on top of the volunteer's standard diet.
|
|
Experimental: Peas
|
One group will consume 400g of standard broccoli each week for 12weeks; the second group will consume 400g of the high glucosinolate broccoli each week for 12weeks while the third group will consume 400g of peas each week for 12weeks.
The broccoli and the peas will be consumed on top of the volunteer's standard diet.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Examination of the indicators of CVD after the consumption of broccoli, high glucosinolate broccoli and peas.
Time Frame: Week 12
|
To examine the effects of a diet rich in broccoli on the systemic indicators of CVD including total cholesterol as well as established physiological measurements such as ambulatory blood pressure (BP), Augmentation Index (AIx) and Pulse Wave velocity (PWV) in subjects with a mild to moderate (10-20%) risk of developing CVD within the next 10 years
|
Week 12
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The determination of key polymorphic genes of the trial subjects
Time Frame: Baseline
|
To determine the genotype of individuals for key polymorphic genes (GSTM1, GSTT1 and GSTP1) and relate them to observed changes in CVD risk.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2010
Primary Completion (Actual)
December 1, 2013
Study Completion (Actual)
December 1, 2013
Study Registration Dates
First Submitted
April 27, 2010
First Submitted That Met QC Criteria
April 30, 2010
First Posted (Estimate)
May 3, 2010
Study Record Updates
Last Update Posted (Estimate)
July 29, 2014
Last Update Submitted That Met QC Criteria
July 28, 2014
Last Verified
July 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2009IFR01
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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