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临床试验/NCT05900609
NCT05900609已完成不适用

Gut Health Enhancement by Eating Favourable Food

VU University of Amsterdam2 个研究点 分布在 1 个国家目标入组 146 人开始时间: 2023年5月22日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
146
试验地点
2
主要终点
Microbiota diversity

研究概览

简要总结

Within the GEEF om je buik study the effects of an 8-week intervention with either a diet rich in fiber or fermented food on the gut microbiota will be investigated.

详细描述

This study is a randomized controlled trial (RCT) with three intervention groups (high dietary fiber group (HDF), high fermented foods group (HFF), and a control group (CG)). The total duration of the study is 5 months and consists of an 8-week intervention (2-week ramp up period with dietary guidelines, followed by 6-week period with dietary guidelines + additional consumption of study products) and a follow-up after 3 months. In total 147 subjects will be included.

研究设计

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

盲法说明

This study is partially blinded, study participants in the fiber and fermented group will be informed about their intervention after randomization. However, the control group will remain blind throughout the intervention period. Furthermore, participants are not made aware of the different types of intervention before start or during the intervention period. This is done to prevent any adjustments of their diets based on the advices in the other groups and to ensure that the control group stays blinded.

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men and Women, aged ≥18 - ≤70 years;
  • Being able to read and speak Dutch;
  • Willing to keep a stable dietary pattern throughout the study, apart from the dietary advice in the study;
  • Having a smartphone compatible with the Lifedata or PocketQ app to fill out the daily questionnaires.

排除标准

  • Having a disease or medical condition which can influence the study results such as diabetes, cancer, diagnosed irritable bowel syndrome, renal disease, liver enzyme abnormality, malignant neoplasm, or a history of inflammatory diseases (such as multiple sclerosis, rheumatoid arthritis, and inflammatory bowel disease);
  • Having a history of intestinal surgery that might interfere with study outcomes (this does not include an appendectomy or cholecystectomy);
  • Average dietary fiber intake of ≥18 gram (women) or ≥22 gram (men) per day, according to the fiber screen questionnaire (see F1 questionnaires);
  • More than 3 servings of fermented foods per day as assessed with the fermented food frequency questionnaire (see F1 questionnaires);
  • Having a Body Mass Index (BMI) of ≥ 30 kg/m2 (self-reported);
  • Currently following a strict diet and unwilling or unable to change; for example, a gluten free diet or a "crash diet" using meal substitutes;
  • Specific food allergies that interfere with dietary intervention (for example, gluten, lactose, etc);
  • Use of prebiotics, probiotics and/or synbiotics (this should be stopped 4 weeks before the start of the study) and use of fiber supplements;
  • Use of antibiotic treatment less than 3 months before start of the study and/or use of antibiotics during the study;
  • Use of medication that can interfere with the study outcomes, as judged by the medical supervisor;
  • Alcoholic use of ≥14 (women) or ≥28 (men) glasses of alcoholic beverages per week;
  • Use of soft or hard drugs (should be stopped at least 4 weeks before start of the study);
  • Being pregnant or lactating;
  • Participation in another clinical trial at the same time;
  • Student or employee working at either Food, Health and Consumer Research from Wageningen Food and Biobased Research, Microbiology at VU, the MLDS, at WholeFiber, Keep Food Simple or at Cidrani;
  • Unable to follow or comply to study rules.

结局指标

主要结局

Microbiota diversity

时间窗: End intervention (week 8)

Microbial richness (ASV) using 16s rRNA

次要结局

  • Gut microbiota composition(End intervention (week 8))
  • Dietary intake(End follow-up (5 months))
  • Stool frequency(Daily during intervention (week 0 - week 8))
  • Abundance of Prevotella(End intervention (week 8))
  • Ratio of Prevotella/Bacteroides(End intervention (week 8))
  • Well-being(End follow-up (5 months))
  • Carbohydrate Active Enzymes (CAZymes)(End intervention (week 8))
  • 92 inflammatory serum proteins(End intervention (week 8))
  • Gastrointestinal complaints(Daily during intervention (week 0 - week 8))
  • Intention to stay healthy (perception + awareness)(End follow-up (5 months))
  • Stool consistency(Daily during intervention (week 0 - week 8))
  • Abundance of Bacteroides(End intervention (week 8))
  • Microbial alpha diversity(End intervention (week 8))
  • Transit time(End intervention (week 8))
  • Sleep quality(End follow-up (5 months))
  • Digestion associated Quality of Life(End follow-up (5 months))
  • Dietary intrinsic motivation (perception + awareness)(End follow-up (5 months))
  • Dietary self-efficacy (perception + awareness)(End follow-up (5 months))
  • Subjective health (perception and awareness)(End follow-up (5 months))
  • Self-regulation (perception + awareness)(End follow-up (5 months))
  • Subjective knowledge (perception + awareness)(End follow-up (5 months))

研究者

发起方
VU University of Amsterdam
申办方类型
Other
责任方
Principal Investigator
主要研究者

Remco Kort

Professor doctor

VU University of Amsterdam

研究点 (2)

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