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Omega (n)-3 PUFA Enriched Beef & Health Outcomes.

Omega (n)-3 PUFA Enriched Beef to Improve Circulating Lipid Concentrations and CVD Risk Markers in Adults: a Randomised Controlled Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03967678
Enrollment
90
Registered
2019-05-30
Start date
2018-11-07
Completion date
2019-04-19
Last updated
2019-06-03

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

Conditions

Cholesterol; Metabolic Disorder, CVD, Inflammation

Keywords

enriched beef, omega, poly unsaturated fatty acids (PUFA), cholesterol, grass fed

Brief summary

Red meat is an integral component of the habitual diet among the UK and Irish population, with adults consuming an average of 71grams/day. Although typically high in saturated fatty acids (SFA), red meat is also an important dietary source of protein and essential nutrients including iron, zinc, B vitamins and long chain n-3 polyunsaturated fatty acids (PUFA) which provide numerous benefits to human health, particularly related to cardiovascular disease (CVD) risk. N-3 and n-6 PUFA are a family of fatty acids with important roles in cardiovascular health, and it is often recommended in dietary guidelines to replace SFA with unsaturated fats, such as PUFA. Owing to the social and economic burden of CVD, increasing the proportions of these unsaturated fatty acids, in combination with a reduction in SFA within meat, could have a large impact on CVD risk at the population level, whilst retaining the beneficial nutrients and n-3 PUFA which meat provides. In this research, a total of 90 eligible and consenting participants will be randomly allocated to consume three portions per week of n-3 enriched beef (from either dietary supplemented or grass-fed cattle) or control beef (from standard supply). This beef will be offered within a lunchtime meal and served from the Human Intervention Studies Unit at Ulster University, Coleraine for a period of 5 weeks. A fasting blood sample will be taken before and after intervention to determine the effect the n-3 enriched beef on cholesterol concentrations, lipid profile, PUFA status and inflammation. Blood pressure, stiffness of the arteries and body shape, size and composition will also be assessed, and some health and lifestyle habits will be captured using questionnaires.

Interventions

DIETARY_SUPPLEMENTThree portions per week (690g beef (raw weight)) for 5 weeks

Lunches served in Human Intervention Studies Unit

Sponsors

Dunbia, Northern Ireland
CollaboratorUNKNOWN
University of Ulster
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

Double blind

Intervention model description

Double blind randomised controlled trial

Eligibility

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

Inclusion criteria

* Free-living, apparently healthy adults * Aged 20+ years at recruitment * Low oily fish consumers (\<2 servings/mo), or those willing to reduce their fish consumption 1 month prior to commencing the study * Non-smokers * Not regularly consuming plant stanols or other n-3 enriched foodstuffs

Exclusion criteria

* Non-free-living adults * Adults \<20 years at recruitment * Oily fish consumers (2 servings/mo or more) * Current smokers * Pregnant/lactating females (or planning to become pregnant) * Food allergy or intolerance that would prevent consumption of the study meals * Diagnosed with a chronic medical condition (such as diabetes; CVD; autoimmune/ inflammatory disorders; cancer) * Prescribed cholesterol or blood pressure lowering medications * Currently taking any fish oil-containing supplement Daily consumption of plant stanols or other n-3 enriched foodstuffs

Design outcomes

Primary

MeasureTime frameDescription
Cholesterol levelsChange at 5 weeks from baselinePlasma cholesterol measured colormetrically

Secondary

MeasureTime frameDescription
Polyunsaturated fatty acid profileChange at 5 weeks from baselineSerum fatty acids measured by GC-MS
Pulse Wave VelocityChange at 5 weeks from baselineMeasured by Sphygmocor XCEL
Lipid profileChange at 5 weeks from baselinePlasma lipids measured colormetrically
Whole body compositionChange at 5 weeks from baselineMeasured by Dual Energy X-ray Absorptiometry
Inflammation statusChange at 5 weeks from baselineMeasured by ELISA
Blood pressureChange at 5 weeks from baselineMeasured by electronic blood pressure monitor

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026