Skip to main content
OpenTrials
Completed

NCT Number: NCT03105947

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

50 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Cambridge

Cambridge, CB2 2QQ, United Kingdom

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Coconut oil

Other

50g extravirgin coconut oil daily for four weeks

Butter

Other

50g butter daily for four weeks

olive oil

Other

50g extra virgin olive oil daily for four weeks

Primary outcomes

  1. LDL-Cholesterol

    Time frame: after 4 weeks of the dietary fat interventions

    Blood LDL cholesterol concentrations

Secondary outcomes

  1. triglycerides

    Time frame: after 4 weeks of the dietary fat interventions

    Blood triglycerides

  2. HDL-Cholesterol

    Time frame: after 4 weeks of the dietary fat interventions

    blood HDL-Cholesterol

  3. total cholesterol

    Time frame: after 4 weeks of the dietary fat interventions

    blood total Cholesterol

  4. weight

    Time frame: after four weeks of the dietary fat interventions

    weight

  5. waist circumference

    Time frame: after four weeks of the dietary fat interventions

    Waist circumference

  6. Systolic Blood pressure

    Time frame: after four weeks of the dietary fat interventions

    systolic blood pressure

Other outcomes

  1. Inflammatory markers

    Time frame: after four weeks of the dietary fat interventions

    Blood inflammatory markers C-Reactive protein

Sponsors and collaborators

Lead sponsor

University of Cambridge

Other

Collaborators

  • British Broadcasting Corporation

Registry information

Official study title

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

Acronym: COB

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Apr 10, 2017
Registry last updated
Oct 27, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.