跳至主要内容
临床试验/NCT05537324
NCT05537324已完成不适用

Effects of a Single Dose of Brazil Nuts on Blood Lipids. A Randomised Controlled Trial.

Skogli Health and Rehabilitation Center1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2016年4月1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
发起方
入组人数
52
试验地点
1
主要终点
Changes in total cholesterol, LDL cholesterol and HDL cholesterol (mmol/l)

研究概览

简要总结

Several studies have shown that regular intake of nuts may improve blood lipids. However, few studies have investigated the effects on blood lipids after a single intake of nuts. The present study was conducted in order to evaluate the acute effects of a single intake of Brazil nuts on blood lipids.

The study was a non-blinded randomized controlled study with 52 participants, 26 participants in both the Brazil nut group and in the control group. Blood tests were taken at baseline and 3h, 6h, 24h, 7d and 14d after ingestion of either 50g Brazil nuts or an isocaloric amount of coconut flakes. We then conducted an unpaired t-test in order to compare changes in blood lipids between the two groups. P-values < 0.05 were considered statistically significant

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Patients who participated in a rehabilitation program over three weeks at a rehabilitation center. Participants were at the rehabilitation center due to rheumatic diseases or chronic pain conditions / fibromyalgia.

排除标准

  • •Food allergy, lactose intolerance, celiac disease, mild illness for the last 3 weeks (infections or inflammatory conditions), serious illness (eg. heart attack) or undergone surgery during the previous 3 months, intake of Brazil four weeks prior study enrollment, using cholesterol-lowering or blood-thinning drugs, planning to eat more than one meal in other places than the rehabilitation center during the study.

研究组 & 干预措施

Coconut

Other

46g Coconut flakes

干预措施: Coconut (Other)

Brazil nut

Experimental

50g Brazil nuts

干预措施: Brazil nut (Other)

结局指标

主要结局

Changes in total cholesterol, LDL cholesterol and HDL cholesterol (mmol/l)

时间窗: Blood tests are measured at baseline, 3 hours, 6 hours, 24 hours, 7 days and 14 days after intervention

Changes in total cholesterol, LDL cholesterol and HDL cholesterol (mmol/l) between the experimental group and the control group at specific times after intervention

次要结局

未报告次要终点

研究者

发起方
Skogli Health and Rehabilitation Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Allan Fjelmberg

Medical director

Skogli Health and Rehabilitation Center

研究点 (1)

Loading locations...

相似试验