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临床试验/NCT03410342
NCT03410342已完成不适用

The Effects of Types of Fruits and Vegetables on Vascular Function in Prehypertensive Participants: a Pilot Study

University of Cambridge2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2017年9月4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
36
试验地点
2
主要终点
Blood pressure

研究概览

简要总结

The CIRCUS study is a randomised controlled, cross-over trial to evaluate the effects of increased intakes of citrus fruits and cruciferous vegetables on vascular function in 36 untreated, prehypertensive participants.

详细描述

The study comprises three 14-day dietary intervention periods, preceded by one week run-in period and separated by one week wash-out periods, 9 weeks in total. The diet will be fully controlled and provided by the researchers. Participants will receive in random order three interventions:

  • 1 portion of fruits plus 1 portion of vegetables, of commonly consumed types per day. Intakes are at 25th percentile of UK consumption and will exclude citrus fruits, cruciferous and allium vegetables.
  • 4 portions of fruits plus 4 portions of vegetables, of commonly consumed types per day excluding citrus fruits, cruciferous and allium vegetables.
  • 4 portions of citrus fruits plus 4 portions of cruciferous vegetables per day.

研究设计

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

入排标准

年龄范围
40 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 40 - 65 years
  • Average systolic blood pressure of 125-140 mmHg at 2 measurements separated by >30 minutes
  • No use of antihypertensive medication
  • No reported current or previous diabetes mellitus, (secondary) hypertension, or metabolic, cardiovascular, renal, liver, thyroid, gastrointestinal diseases
  • Body Mass Index between 20 - 35 kg/m2
  • Non-smoker
  • Average fruit and vegetable consumption of <4 portions per day (UK average, 40-65 years), or willing to reduce habitual daily fruit and vegetable intake.

排除标准

  • Any medication likely to interfere with energy metabolism, appetite regulation and hormonal balance.
  • Excessive alcohol intake of > 21 units per week (females) or >28 units per week (male) and not willing to limit alcohol intake to maximum of 1 unit/day
  • Physical activity of >=10 hours/week of moderate to vigorous physical activity
  • Weight loss or gain of >=3 kg in the preceding 3 months
  • Use of dietary supplements or unwilling to stop supplement use >= 2 weeks before enrolment and during intervention
  • Pregnancy or lactation
  • Intervention specific factors, including:
  • Unable or unwilling to consume provided diets during the intervention
  • Unsufficient storage space for provided diets
  • Food sensitivities or vegetarian/vegan diet by choice
  • Participation in another intervention study at the same time
  • Living > 15 miles from the Imperial/NIHR Clinical Research Facility at Hammersmith Hospital
  • No signed informed consent

研究组 & 干预措施

Low Fruits and Vegetables (LFV)

Placebo Comparator

1 portion of fruits plus 1 portion of vegetables, of commonly consumed types per day.

Intakes are at 25th percentile of UK consumption (NDNS) and will exclude citrus fruits, cruciferous and allium vegetables.

干预措施: LFV (Other)

High Fruits and Vegetables (HFV)

Experimental

4 portions of fruits plus 4 portions of vegetables, of commonly consumed types per day excluding citrus fruits, cruciferous and allium vegetables.

干预措施: HFV (Other)

High Citrus fruits and Cruciferous vegetables (CC)

Experimental

4 portions of citrus fruits plus 4 portions of cruciferous vegetables per day excluding any other types of fruits and vegetables including allium vegetables.

干预措施: CC (Other)

结局指标

主要结局

Blood pressure

时间窗: Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks

Changes in systolic and diastolic blood pressure (mmHg) measured by automated oscillometric device (average of 3 measurements).

次要结局

  • Markers of low-grade inflammation measured in fasted blood samples(Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks)
  • Urinary metabolic profiles(Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks)
  • Arterial stiffness(Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks)
  • Established objective markers of food intake(Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks)
  • Faecal microbiome composition(Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks)
  • Circulatory metabolic profiles(Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks)
  • Markers of cardiometabolic health measured in fasted blood samples(Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks)
  • Markers of endothelial function measured in fasted blood samples(Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks)
  • Self-rated general health and mental well-being(Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks)
  • Cognitive function(Measured on the morning after each of three recurring run-in periods and after each of three recurring 2-week intervention periods, 6 times total during 9 weeks)

研究者

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

Linda Oude Griep

Senior Research Associate

University of Cambridge

研究点 (2)

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