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临床试验/NL-OMON52304
NL-OMON52304已完成不适用

The effect of alternating energy intake compared to regular energy intake on the fat content in the blood after a meal in abdominally obese adults - Alternating energy intake and blood fat content after a meal

niversiteit Maastricht0 个研究点目标入组 23 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
23

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • * Apparently healthy men and women as judged by study physician
  • * Abdominally obese males (waist circumference * 102 cm) and females (waist
  • circumference * 88 cm)
  • * Aged between 18 * 75 years
  • * Stable bodyweight (weight gain or loss * 3 kg in the past three months)
  • * Willingness to give up being a blood donor (or having donated blood) from 8
  • weeks before the start of the study, during the study and for 4 weeks after
  • completion of the study
  • * Women should be pre- or postmenopausal
  • * No difficult venipuncture as evidenced during the screening visit
  • * Sedentary (light exercise < 1 h per week) or moderately active (moderate
  • exercise 1-2 h per week)
  • * Having a general practitioner
  • * Agreeing that the participant and general practitioner will be informed about
  • medically relevant personal test results by a physician
  • * Willing to comply to study protocol during study
  • * Informed consent signed

排除标准

  • * Fasting plasma glucose * 7 mmol/l
  • * Fasting serum triacylglycerol * 4.5 mmol/l
  • * Fasting serum total cholesterol * 8 mmol/l
  • * Blood pressure * 160/100 mm Hg
  • * Current smoker, or smoking cessation < 12 months
  • * Drug abuse
  • * Alcohol abuse (* 21 alcohol consumptions per week)
  • * Use of medication known to affect blood pressure, serum lipid metabolism, or
  • glucose metabolism
  • * Having a medical condition or history which might impact study measurements,
  • to be judged by the study physician (e.g. myocardial infarction, angina,
  • thrombosis, stroke, cancer, familiar hypercholesterolemia, liver or bowel
  • disease or diabetes)
  • * Active cardiovascular disease like congestive heart failure or cardiovascular
  • event, such as an acute myocardial infarction or cerebrovascular accident
  • * Use of an investigational product within another biomedical intervention
  • trial within the previous 1-month
  • * Women who are perimenopausal, have an irregular menstrual cycle, or are
  • * Use of over-the-counter and prescribed medication, which may interfere with
  • study measurements (to be judged by the principal investigator), e.g. weight
  • loss medication
  • * Reported dietary habits: medically prescribed diets or slimming diets
  • * Reported participation in night shift work 2 weeks prior to screening and/or
  • during the study. Night work is defined as working between midnight and 6.00 AM

研究者

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