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Diet and Vascular Health Study

Diet and Vascular Health Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01114399
Acronym
BROCCOLI
Enrollment
48
Registered
2010-05-03
Start date
2010-01-31
Completion date
2013-12-31
Last updated
2014-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Disease

Keywords

Cardiovascular Disease, Cardiovascular Disease risk (mild to moderate), Cholesterol, Ambulatory blood pressure, Arterial Stiffness

Brief summary

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.

Interventions

DIETARY_SUPPLEMENTDiet and Vascular Health

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.

DIETARY_SUPPLEMENTDiet and Vascular Health Study

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.

Sponsors

Clinical Research and Trials Unit (Norfolk & Norwich University Hospital, UK)
CollaboratorOTHER
University of East Anglia
CollaboratorOTHER
Quadram Institute Bioscience
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Examination of the indicators of CVD after the consumption of broccoli, high glucosinolate broccoli and peas.Week 12To 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

Secondary

MeasureTime frameDescription
The determination of key polymorphic genes of the trial subjectsBaselineTo determine the genotype of individuals for key polymorphic genes (GSTM1, GSTT1 and GSTP1) and relate them to observed changes in CVD risk.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 22, 2026