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临床试验/NCT06749327
NCT06749327尚未招募不适用

Ultra-processed Foods, Diet Quality, and Cardiometabolic Health

Queen's University, Belfast4 个研究点 分布在 2 个国家目标入组 330 人开始时间: 2026年10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
尚未招募
入组人数
330
试验地点
4
主要终点
Glycated haemoglobin (HbA1C) (mmol/mol)

研究概览

简要总结

Controversy remains around the role of ultra-processed food (UPF) consumption and health outcomes. A key question that remains to be answered is: when diet quality is the same, does food processing itself have any independent health effects? The current application aims to isolate the health effects of food processing from those of diet quality through the conduct of a dietary intervention study.

详细描述

Controversy remains around the role of UPF consumption and health outcomes. A key question that remains to be answered is: When diet quality is the same, does food processing itself have any independent health effects?

The current study aims to isolate the health effects of food processing from those of diet quality through the conduct of a dietary intervention study.

To isolate the health effects of food processing, the investigators propose to use healthy plant-based diets as the "base" diet. The investigators propose to initially discover plasma metabolomic features responsive to improved hPDI adherence and then conduct a dietary intervention trial to evaluate the impact of UPF consumption, in the setting of a high hPDI diet, on cardiometabolic outcomes and metabolic pathways.

The study will consist of a run-in phase where participants with a low adherence to a plant based diet will be randomized into (1) an intervention group that will receive diet counselling to follow a high hPDI diet over a period of 6 weeks and (2) a control group that will consume their usual diet (low hPDI). Both arms will be advised to avoid ultra processed food (UPF) consumption. Assuming 15% attrition, the study will enrol 118 participants for the run-in phase. Individuals with a high adherence to plant based diet will follow their normal diet for the 6 weeks of this run-in phase and then will be randomised into the main 4 month study.

In the main four month study, a randomized controlled parallel group dietary intervention will be conducted in participants with high hPDI in Ireland (North and South) to evaluate the impact of UPF consumption, in the context of a high hPDI diet, on cardiometabolic outcomes such as glycated haemoglobin and total cholesterol, and metabolic pathways. Participants will be randomized into one of 2 groups: high UPF hPDI diet or low UPF hPDI diet. Assuming an attrition rate of 15%, the study will enrol ~212 individuals to achieve a sample size of 180 participants who will complete the trial.

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
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Men and women aged between 18 and 65 years in general good health with BMI < 35 kg/m2 who can provide informed consent.

排除标准

  • Participants will be ineligible to enrol if they have diabetes, CVD, any type of cancer (except for basal cell skin cancer), or a condition (pregnancy, breastfeeding, etc) or dietary restriction(s) that would substantially limit their ability to complete the study.
  • Individuals will be screened for their adherence to the Plant based diet Index (PDI ).
  • Individuals with low adherence will enter run-in phase only (6 weeks)
  • Individuals with high adherence will enter the main intervention (4 months)

研究组 & 干预措施

High UPF, high hPDI diet

Experimental

High ultra-processed foods (UPFs) and healthy plant based diet

干预措施: High UPF, high hPDI diet (Behavioral)

Low UPF, high hPDI diet

Active Comparator

Low ultra-processed foods (UPFs) and high healthy plant-based diet

干预措施: Low UPF, high hPDI diet (Behavioral)

结局指标

主要结局

Glycated haemoglobin (HbA1C) (mmol/mol)

时间窗: Baseline and 4 months

Change in HbA1c over the course of the 4 month intervention.

Total cholesterol (mg/dL)

时间窗: Baseline and 4 months

Change in total cholesterol will be measured over the course of the 4 month intervention.

次要结局

  • Anthropometric measure: Weight (kg)(Baseline and 4 months)
  • Anthropometric measure: Height (m)(Baseline and 4 months)
  • Anthropometric measure: Hip circumference (cm)(Baseline and 4 months)
  • Anthropometric measure: Waist circumference (cm)(Baseline and 4 months)
  • Blood pressure (mmHg)(Baseline and 4 months)
  • Dietary assessment(Baseline and 4 months)
  • Physical activity(Baseline and 4 months)
  • Plasma metabolome(Pre and post run-in phase (6 week run-in) ; baseline and 4 months (main trial))
  • Demographic/lifestyle information(Baseline and 4 months)
  • Continuous Glucose Monitoring (mmol/L)(Baseline and 4 months)
  • Gut microbiome(Baseline and 4 months)
  • Inflammatory markers e.g. CRP (mg/L)(Baseline and 4 months)

研究者

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

Jayne Woodside, PhD

Professor

Queen's University, Belfast

研究点 (4)

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