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Identifying Wearable Biomarkers to Monitor Dietary Intake

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Contents

clinicaltrials.gov/study/NCT06398340
Is a
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Clinical study
0

Clinical Study attributes

NCT Number
NCT063983400
Health Conditions in Trial
Metabolism
Metabolism
0
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Digestion
0
Trial Recruitment Size
100
Trial Sponsor
Imperial College London
Imperial College London
0
Clinical Trial Start Date
May 1, 2024
0
Primary Completion Date
December 31, 2024
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Study Completion Date
July 31, 2025
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Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Basic Science0
Intervention Type
Other0
Interventional Trial Phase
Not Applicable0
Official Name
Identifying Physiological Biomarkers for Monitoring Dietary Behaviours0
Last Updated
May 6, 2024
0
Allocation Type
Randomized0
Intervention Model
Crossover Assignment0
Masking Type
Single0
Masked Party
Participant0

Other attributes

Intervention Treatment
High Calorie Meal Intervention0
Low Calorie Meal Intervention0
Study summary

Background: Measuring what people eat is a challenge in nutrition research. Traditional methods, like food diaries, rely on self-reporting of individuals, and suffer from poor accuracy and recall bias. Aims: This project aims to identify physiological biomarkers related to food and energy intake, which may be used to develop an objective tool to estimate individuals' food intake in future. Eating behaviours are accompanied by significant physiological changes such as skin temperature, blood oxygen saturation, pulse rate etc. The investigators intend to investigate whether monitoring these physiological changes can help us estimate eating behaviour, such as meal size, eating speed, and duration of meals. Study design: Ten healthy adults will be invited for two study visits at NIHR Imperial Clinical Research Facility. Each visit will last for approximately 2 hr. They will consume a high- and low-calorie meal designed by nutritional researchers in a randomised order. During eating events, the investigators will track their physiological changes via a bedside monitor and wearable sensors. Blood samples will be taken from participants to measure their glycaemic response. Associations between energy load, glycaemic response, and physiological changes will be investigated. Our findings may promote an accelerated development of a wearable tool for dietary assessment in future.

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