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Trial of Different Dietary Fats on Blood Lipids and Metabolic Measures in Healthy Participants

Randomized Trial of Coconut Oil, Butter or Olive Oil on Blood Lipids and Metabolic Measures in Healthy Participants

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03105947
Acronym
COB
Enrollment
94
Registered
2017-04-10
Start date
2017-06-22
Completion date
2017-08-10
Last updated
2017-10-27

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

Conditions

Cardiovascular Risk Factor

Keywords

lipids, dietary fats

Brief summary

This is a randomised trial in which healthy volunteers, men and women aged 50-75 years from the general community are randomized into one of three arms: participants will be provided with 50 gm extra virgin coconut oil,or 50 grams butter or 50 extra virgin olive oil to be eaten daily for a month. The key outcome is blood low density lipoprotein cholesterol concentrations and secondary outcomes blood lipid profile (total cholesterol, high density lipoprotein cholesterol, triglycerides) and anthropometric measures: weight and waist circumference. This trial is powered to detect a difference of 0.5 mmol/L LDL-cholesterol difference between the trial arms.

Detailed description

This is a randomized trial in which healthy volunteers from the general community are randomized into one of three arms: consumption of 50 gm of extra virgin coconut oil daily OR 50gm of butter daily OR 50gm of extra virgin olive oil daily (50gm is about 2 ounces, or 2 table spoons), to be consumed over a one month period. The research participants will be recruited from the general community through advertising (BBC). After full informed consent, participants will attend an assessment visit and have a baseline measures of weight, height, waist circumference, blood pressure, a blood sample for assessment of blood lipids and other metabolic markers, and fill in a health questionnaire and dietary questionnaire. Participants will be randomly allocated to one of three arms: coconut oil, butter or olive oil and will be given supplies of these (portioned, or with measuring spoons) with information about daily consumption of 50 gram of one of these fats. After one month, participants will return for follow up assessment which will include a repeat blood sample, anthropometric measures and blood pressure, and questionnaire. Blood samples collected by venepuncture will be stored at the University of Cambridge and analysed at the Department of Clinical Biochemistry, Cambridge University Addenbrooke's Hospital. At the end of the study, all participants will be given the individual participant results of the anthropometric measures and lipid profiles at baseline and follow up as well as the overall findings of the trial.

Interventions

OTHERCoconut oil

50g extravirgin coconut oil daily for four weeks

OTHERButter

50g butter daily for four weeks

OTHEROlive oil

50g extra virgin olive oil daily for four weeks

Sponsors

British Broadcasting Corporation
CollaboratorINDUSTRY
University of Cambridge
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Masking description

The primary outcome will be blood LDL-cholesterol, secondary outcomes, lipid profile which will be measured in a biochemistry lab by individuals who have no knowledge of the allocation to intervention arms.

Intervention model description

Randomized trial of different dietary fats

Eligibility

Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Willing to participate in the trial of dietary interventions for one month within the age range

Exclusion criteria

* No known cardiovascular disease: heart disease or stroke; no known cancer; no known diabetes; no use of lipid lowering medication eg. statins; no contraindications to high fat diet e.g. gall bladder or other gastrointestinal condition

Design outcomes

Primary

MeasureTime frameDescription
LDL-Cholesterolafter 4 weeks of the dietary fat interventionsBlood LDL cholesterol concentrations

Secondary

MeasureTime frameDescription
HDL-Cholesterolafter 4 weeks of the dietary fat interventionsblood HDL-Cholesterol
total cholesterolafter 4 weeks of the dietary fat interventionsblood total Cholesterol
weightafter four weeks of the dietary fat interventionsweight
triglyceridesafter 4 weeks of the dietary fat interventionsBlood triglycerides
Systolic Blood pressureafter four weeks of the dietary fat interventionssystolic blood pressure
waist circumferenceafter four weeks of the dietary fat interventionsWaist circumference

Other

MeasureTime frameDescription
Inflammatory markersafter four weeks of the dietary fat interventionsBlood inflammatory markers C-Reactive protein

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026