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Diet and Vascular Health

Not Applicable
Completed
Conditions
Topic: Primary Care Research Network for England, Cardiovascular
Subtopic: Not Assigned, Cardiovascular (all Subtopics)
Disease: Cardiovascular, All Diseases
Circulatory System
Cardiovascular disease
Registration Number
ISRCTN20997112
Lead Sponsor
Institute of Food Research (UK)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
54
Inclusion Criteria

1. Men and women aged greater than or equal to 50 years
2. Recruited onto the study using the JBS cardiac risk assessor calculator. Scores of 1020% will be acceptable for participation in the study.
3. Total cholesterol greater than or equal to 5.0 mmol/L
4. Blood pressure measurements: systolic greater than or equal to 120 mmHg, diastolic greater than or equal to 80 mmHg
5. Body mass index (BMI) greater than 20 kg/m^2

Exclusion Criteria

1. Diagnosed diabetics
2. Fasting glucose greater than 6 mmol/L
3. Blood pressure less than 90/50 mmHg or 95/95 mmHg if symptomatic; greater than 160/100 mmHg
4. Chronic kidney disease
5. Those on hypolipidemic therapy
6. Those who have suffered a cardiovascular event like stroke, myocardial infarction, trans ischemic attacks etc within 2 years
8. Peripheral vascular disease including claudication
9. Consumption of fish oil supplements (unless volunteer is willing to discontinue their use at least 4 weeks prior to intervention starting)
10. Parallel participation in another research project which involves dietary intervention and/or sampling of biological fluids/materials
11. Any person related or living with any member of the study team
12. Participation in another research project which involves blood sampling within the last four months; blood from both studies should not exceed 470 mL
13. BMI less than 20 kg/m^2 or BMI greater than 40 kg/m^2
14. Fasting total cholesterol greater than 8.0 mmol/L
15. Gastrointestinal disease (excluding hiatus hernia) unless symptomatic or study intervention/procedure is contraindicated
16. Going on holiday for more than 7 days in any single period or within 2 weeks of their clinical appointment at the CRTU
17. Currently suffering from or have suffered from any neck and throat injuries and surgery

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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