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临床试验/NCT03105947
NCT03105947已完成不适用

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

University of Cambridge2 个研究点 分布在 1 个国家目标入组 94 人开始时间: 2017年6月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
94
试验地点
2
主要终点
LDL-Cholesterol

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Outcomes Assessor)

盲法说明

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.

入排标准

年龄范围
50 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • 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

研究组 & 干预措施

Butter

Active Comparator

50g butter to be consumed daily for four weeks

干预措施: Butter (Other)

Coconut oil

Active Comparator

50g extra virgin coconut oil to be consumed daily for four weeks

干预措施: Coconut oil (Other)

Olive Oil

Active Comparator

50g extra virgin olive oil to be consumed daily for four weeks

干预措施: Olive oil (Other)

结局指标

主要结局

LDL-Cholesterol

时间窗: after 4 weeks of the dietary fat interventions

Blood LDL cholesterol concentrations

次要结局

  • triglycerides(after 4 weeks of the dietary fat interventions)
  • HDL-Cholesterol(after 4 weeks of the dietary fat interventions)
  • total cholesterol(after 4 weeks of the dietary fat interventions)
  • weight(after four weeks of the dietary fat interventions)
  • waist circumference(after four weeks of the dietary fat interventions)
  • Systolic Blood pressure(after four weeks of the dietary fat interventions)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kay-Tee Khaw

Professor of Clinical Gerontology

University of Cambridge

研究点 (2)

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