Dietary Intake AssessmentSODIAT-2NCT06879574
Identifying the Best Tools for Recording Diet in Free-living UK Adults (SODIAT-2 Study)
An observational study of Dietary Intake Assessment and Food Intake Measurement, run by University of Reading at 4 sites in United Kingdom.
Trial summary
The aim of the SODIAT-2 study is to evaluate the effectiveness of dietary intake assessment tools in a real-world setting. These tools include wearable cameras, spot urine samples, capillary blood samples, and a web-based food frequency questionnaire (FFQ). Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Dietary Intake Assessment, Food Intake Measurement
- What is being tested?
- Measuring dietary intake
- How many people
- 150 participants
- Where
- 4 sitesUnited Kingdom
- Study dates
- 25 Aug 2025to 17 Aug 2026
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: UK population.
Who may be able to join
- 18 years and older
- Lives in Great Britain (England, Schotland and Walse)
- Able to read/understand instructions written in English and are fluent in English
Who cannot join
- Diagnosed or self-report as being underweight (have a body mass index (BMI) of less than 18.5 kg/m2)
- Are unwilling/unable to collect urine and blood samples, use the wearable camera as instructed and/or spend 20-30 min online recording what they've recently had to eat/drink on multiple occasions
- Are unwilling/unable to have a video call with a researcher with cameras turned on
- Are unwilling/unable to post samples on specific days and receive/send a larger parcel at the start/end of the study (note: all return packaging and postage will be provided by us and will include a courier delivery and collection)
- Are unwilling/unable to receive a single grocery delivery from Sainsbury's or Tesco online supermarkets (delivery to be arranged by us), includes living in a postcode area that cannot receive grocery deliveries from Tesco or Sainsburys as well as not having space to refrigerate and freeze items.
- Are unwilling/unable to eat/drink any items on the calibration menu, e.g., food allergies/intolerances, dislike of food items, unable eat (e.g. vegan or have to avoid for a medical condition) or cannot eat 3 meals plus snacks daily (note: vegetarians can take part)
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- Are unwilling/unable to avoid taking dietary and herbal supplements for at least 1 week before and during the 5-week study (e.g. fish oils, vitamins, iron, protein shakes, nutrient powders, joint care)
- Are pregnant, may be pregnant or breast-feeding
- Currently experiencing, recovering or at a high risk of an eating disorder (e.g., previous diagnosis, or concerns that you have an unhealthy relationship with food)
- Have a health condition, are taking medication and/or undergoing medical treatment that affects metabolism, appetite and/or ability to eat the calibration menu (e.g. cancer, chemotherapy, diabetes, gastrointestinal disorders (such as inflammatory bowel disease, Crohn's disease), kidney disease, liver disease, HIV or AIDS)
- Are taking any of the following medications: androgens, blood thinners, phenytoin, erythromycin, or thyroid hormones
- Long-term use of any of the following medications: anti-inflammatories (NSAIDS), steroids/corticosteroids or antibiotics (eligible following a 4-week washout after short term use; eligible if use is infrequent)
- Use illicit substances/recreational drugs
- Have been diagnosed with dementia or other conditions affecting memory
- Do not have anyone at home, work, etc. to help them if they require assistance to use the study tools (such as arthritis, Parkinson's disease, sight loss, etc.)
- If the participants have recently taken part in another intervention study, a 4-week washout will be required before they are able to start the study.
Trial locations and contacts
4 sites in 1 country.
United Kingdom4 sites
Department of Life Sciences, Aberystwyth University
Aberystwyth, SY23 3DA
University of Cambridge, Pathology building level 4, Addenbrooke's Hospital
Cambridge, CB2 0QQ
Nutrition Research Section, Hammersmith Hospital Campus, Imperial College
London, W12 0NN
Hugh Sinclair Unit of Human Nutrition, University of Reading
Reading, Berkshire, RG6 6DZ
About this study
Official title: Investigating a Data-driven Standardized and Objective Dietary Intake Assessment Tool in Free-living Individuals - SODIAT-2 Study
The aim of the SODIAT-2 study is to evaluate the effectiveness of dietary intake assessment tools in a real-world setting. These tools include wearable cameras, spot urine samples, capillary blood samples, and a web-based food frequency questionnaire (FFQ). The main questions it aims to answer are:
Is the accuracy of dietary assessment improved in free-living environments when a combination of subjective and objective assessments tools are used?
Read more
Secondary research questions are:
Can wearable cameras accurately monitor the daily dietary intake of free-living individuals? Does a combination of capillary blood samples and spot urine samples provide a robust assessment of the nutrient status and habitual dietary exposure in a free-living setting? Can data-driven integration of multiple emerging technologies create a dietary assessment tool that is low burden, accurate and scalable in free-living populations? Can a condensed FFQ estimate diet quality as effectively as a detailed FFQ?
Participants will:
Use the dietary assessment tools (wearable camera, spot urine, capillary blood, and eNutri FFQ web-app) as instructed over a 5-week period from their home and/or working space.
Take part in two monitoring weeks (week 1 and week 5) where they will record their usual dietary intake over 3 days.
Consume an identical 3-day study meal plan during the test (calibration) diet week 3, whilst repeating the monitoring week measurements.
This study aims to recruit 133 adults living in Great Britain (GB) to better understand how these tools perform outside of a clinical environment.
Read the detailed description
The SODIAT project is a collaborative effort involving Aberystwyth University (AberU, project lead), University of Reading (UoR), Imperial College London (Imperial), and the University of Cambridge (UoC). Study 1, completed in July 2024, assessed the effectiveness of objective and subjective dietary intake assessment methods in highly-controlled clinical trial (protocol published at https://doi.org/10.12688/f1000research.155683.1) and informed the design of study 2.
Study 2 is led and sponsored by UoR. All study activities will be conducted remotely, with participants taking part from their usual locations (e.g., home, work).
►Screening and Welcome Week
Participants will use the online REDCap research platform to provide informed consent and complete a screening questionnaire to determine eligibility. Eligible participants will be contacted by a study researcher to discuss the study requirements, confirm consent, and schedule the study period.
A week before starting the 5-week study (Welcome Week), participants will be sent study materials/equipment and will be referred to the SODIAT webpage to view online video tutorials and read user guidelines for each study tool. Afterwards, participants will attend a video call with a study researcher to familiarize them with the study protocol and provide an opportunity to ask questions.
During the Welcome Week, participants will also self-collect a baseline blood sample (pre-video call) and complete the online eNutri FFQ to assess habitual diet. Within 2 days, they will then complete a condensed version of the FFQ to evaluate its effectiveness in estimating diet quality with reduced participant burden.
►5-week study period
Participants will follow their usual diet during weeks 1 \& 5 and record their diet using study tools (wearable cameras, blood samples, urine samples and online FFQ) for 3 consecutive days (Monitoring Weeks). During week 3 (Calibration Week), participants will use the same study tools as before whilst consuming the 3-day test diet. There will be two test diets (one diet for meat/fish consumers and another slightly adapted for non-consumers), consisting of foods and drinks that are common in the UK. During this controlled part of the study, participants will be requested to eat/drink all foods and drinks provided (delivered by an online supermarket) but cannot consume anything extra. They will receive recommendations on serving sizes for each food/drink but participants can choose how much they eat (either more or less).
►Wearable cameras
Participants will wear a small camera unit mounted on glasses (or attached to their own frames) during the 3-day periods of weeks 1, 3, and 5 (days 1-3; 15-17 and 32-34). The camera automatically captures still images every 7 seconds to document food and drink intake. The camera will be worn from waking to going to bed, although participants will be instructed to remove the camera during private times (e.g., bathroom), sensitive locations (e.g., changing rooms, GP surgeries) and if unsafe to wear (e.g., driving), and log these occasions, as well as the camera start time, on a paper-based log. At the end of the study, encrypted SD cards containing the images will be returned to the research team at Imperial for secure processing.
Images will be pre-processed using AI to exclude irrelevant images, and blur identifying details (e.g., faces, device screens). Only anonymised images will be analysed by researchers to estimate dietary intake.
►Capillary blood samples
When fasted, participants will self-collect blood samples using OneDraw kits on day 4 of each study week (day 4, 18 and 35), which collect a few drops of blood from the upper arm/thigh onto a filter paper cartridge. A baseline sample will also be collected during the Welcome Week. Instructions and video tutorials will be provided, and samples will be mailed to researchers at UoC for storage and biomarker analysis.
►Spot urine samples
Over 4 consecutive days of each study week (days 1-4, 15-18, 32-35), participants will collect first morning void and last evening void urine samples using straw and vacuum tube kits. Samples will be temporarily stored in a refrigerator before mailing them to AberU for processing where biomarkers of food and drink intake will be analysed.
►Online FFQ (eNutri)
Participants will complete the online eNutri FFQ on six occasions. Both the original (long-format) and condensed FFQ will be completed during Welcome Week to capture habitual intake during the previous 4 weeks. During the study, a 3-day, condensed FFQ adapted to capture foods/drinks not well-represented by biomarker analysis, will be completed at the end of each recording week (day 4, 18 and 35). During the test diet week, the original FFQ, adapted to capture 3-day intakes, will also be completed (day 18). The FFQ inputs, nutrient and food group intakes, and diet quality data will be exported in pseudonymised format for analysis.
At the study's conclusion, participants will complete a short, online usability questionnaire about the study tools via REDCap (day 35).
Participants will mail their blood and urine samples at designated timepoints using pre-paid postage, and return all study equipment and logs at the end of the study via a courier collection.
Researchers will monitor adherence and communicate with participants as needed. Daily reminders will also be sent via email or text (SMS) message during the recording days.
► Statistical analysis
Accuracy of integrating multiple dietary assessment technologies to report dietary intake in free living environments will be measured during the calibration week (week 3) using dietary intake data collected from wearable cameras, spot urine samples, capillary blood samples, and self-reported FFQs.
- Conditions
- Dietary Intake Assessment, Food Intake Measurement
- Being tested
- Measuring dietary intake
- Keywords
- Nutrition, Health, Dietary reporting, Misreporting
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Measuring dietary intakeOther
During 5-week study, participants will monitor their usual dietary intake during two 3-day periods (on weeks 1 and 5). During week 3 (calibration week) participants will consume a test diet. Wearable camera technology, self-collected blood and urine samples, and online FFQ (eNutri) will be used to monitor food intake during study weeks. Study tools as well as foods/drinks for the test diet will be delivered to each participant and they will be asked to comply with the study procedures in their home or working environment. Participants will post study samples and the study equipment/logs at designated times using pre-paid envelopes or a courier collection, respectively.
| Study group | Role | What they receive |
|---|---|---|
| Free-living adults living in GB | The study aims to recruit 133 adults living in GB with BMI more than 18.5 kg/m2 who are fluent in English. Participants will monitor their usual dietary intake during two 3-day monitoring periods during weeks 1 and 5 by wearing camera technology, self-collecting blood and urine samples at designated times, and completing online food frequency questionnaire on multiple occasions. During the calibration week (week 3) participants will consume the same 3-day test diet (either the diet for meat/fish consumers or non-consumers, as identified at screening). Receives: Other: Measuring dietary intake |
What is being measured
The primary outcome is the main question the study is designed to answer.
Dietary intake measured by wearable camera technology.
Wearable cameras will be worn by the participants during the study days. Images from wearable cameras will be analysed to estimate what foods and drinks were consumed during the study days, as well as estimating their portion sizes (grams per day).
Measured: Days 1- 3 (week 1), days 15-17 (week 3) and days 32-34 (week 5).
Dietary intake measured by spot urine.
A range of biomarkers indicating what a person has eaten/drank will be measured in urine samples.
Measured: Morning and evening spot urine samples collected over 4 consecutive days on weeks 1, 3 and 5 (days 1-4, 15-18, 32-35).
Dietary intake measured by blood sample.
A range of food/drink biomarkers will be measured in capillary blood samples to indicate what a person has eaten/ drank.
Measured: Samples collected at fasted state in the morning of days 4, 18 and 35 (weeks 1, 3 and 5).
Monitoring/calibration week dietary intake (condensed 3-day FFQ).
Food/drink intake during the 3-day study periods will be measured by the 3-day condensed FFQ (adapted to capture foods not represented by biomarker analysis). Outcomes include dietary intakes (frequency, portion size and grams per day) for each FFQ item, nutrient intakes, food group intakes and diet quality score.
Measured: Days 4, 18 and 35 (weeks 1, 3 & 5).
Secondary outcomes (4)
Habitual dietary intake (original eNutri FFQ).
Habitual intake will be measured by the original 4-week eNutri FFQ. Outcomes include dietary intakes (frequency, portion size and grams per day) for each FFQ item, nutrient intakes, food group intakes and diet quality score.
Measured: Baseline.
Habitual dietary intake (condensed original FFQ).
Habitual intake will be measured by the condensed 4-week eNutri. Outcomes include dietary intakes (frequency, portion size and grams per day) for each FFQ item, nutrient intakes, food group intakes and diet quality score.
Measured: Baseline, after original eNutri FFQ.
Calibration week dietary intake (3-day eNutri FFQ).
Food/drink intake during the 3-day calibration week ( week 3) will be measured by the 3-day FFQ. Outcomes include dietary intakes (frequency, portion size and grams per day) for each FFQ item, nutrient intakes, food group intakes and diet quality score.
Measured: Day 18, week 3.
Usability questionnaire for each research tool.
Short qualitative feedback questionnaire will be administered online via REDCap to determine participants' perspectives on usability of each study tool (including Likert scale questions "strongly disagree to strongly agree" and free text responses).
Measured: Day 35, week 5.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Mar 2025
- Study start25 Aug 2025
- Primary completion17 Aug 2026
- Study completion17 Aug 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Dietary Intake AssessmentStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Prospective
- Enrolment
- 150 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Reading
- Sponsor type
- University, hospital or other
- Collaborators
- Aberystwyth University, University of Cambridge, Imperial College London
- Responsible party
- Principal investigator, Julie Lovegrove, University of Reading
- Investigators
- Manfred Beckmann, Dr, Principal investigator, Department of Life Sciences, Aberystwyth UniversityJulie A Lovegrove, Professor, Principal investigator, Hugh Sinclair Unit of Human Nutrition Department of Food and Nutritional Sciences, University of ReadingGary Frost, Professor, Principal investigator, Nutrition Research Section, Hammersmith Hospital Campus, Imperial College
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06879574
- Sponsor's protocol ID
- UREC 24/43
- Other IDs
- (MR/W028336/1)
- Acronym
- SODIAT-2
- Status last verified
- Aug 2026
- First submitted
- 24 Feb 2025
- Last updated
- 16 Sep 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Anonymised individual participant data will be shared in accordance with confidentiality and consent agreements. This may include: sociodemographic information, anthropometric measurements, dietary intake data, blood and urine biomarkers. Public data repositories (to be agreed by the project team) will be used preserving fully anonymised individual data.
Study at a glance
From the registry record, last updated by the sponsor on 16 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Investigating a Data-driven Standardized and Objective Dietary Intake Assessment Tool in Free-living Individuals - SODIAT-2 Study
- ClinicalTrials.gov ID
- NCT06879574
- Acronym / sponsor ID
- SODIAT-2 / UREC 24/43
- Conditions
- Dietary Intake Assessment, Food Intake Measurement
- Keywords
- Nutrition, Health, Dietary reporting, Misreporting
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 150 participants (actual)
- Lead sponsor
- University of ReadingUniversity, hospital or other
- Collaborators
- Aberystwyth University, University of Cambridge, Imperial College London
- Study start
- 25 Aug 2025 (actual)
- Primary completion
- 17 Aug 2026 (actual)
- Study completion
- 17 Aug 2026 (actual)
- First posted
- 17 Mar 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of the SODIAT-2 study is to evaluate the effectiveness of dietary intake assessment tools in a real-world setting. These tools include wearable cameras, spot urine samples, capillary blood samples, and a web-based food frequency questionnaire (FFQ). The main questions it aims to answer are:
Is the accuracy of dietary assessment improved in free-living environments when a combination of subjective and objective assessments tools are used?
Secondary research questions are:
Can wearable cameras accurately monitor the daily dietary intake of free-living individuals? Does a combination of capillary blood samples and spot urine samples provide a robust assessment of the nutrient status and habitual dietary exposure in a free-living setting? Can data-driven integration of multiple emerging technologies create a dietary assessment tool that is low burden, accurate and scalable in free-living populations? Can a condensed FFQ estimate diet quality as effectively as a detailed FFQ?
Participants will:
Use the dietary assessment tools (wearable camera, spot urine, capillary blood, and eNutri FFQ web-app) as instructed over a 5-week period from their home and/or working space.
Take part in two monitoring weeks (week 1 and week 5) where they will record their usual dietary intake over 3 days.
Consume an identical 3-day study meal plan during the test (calibration) diet week 3, whilst repeating the monitoring week measurements.
This study aims to recruit 133 adults living in Great Britain (GB) to better understand how these tools perform outside of a clinical environment.
Detailed description
The SODIAT project is a collaborative effort involving Aberystwyth University (AberU, project lead), University of Reading (UoR), Imperial College London (Imperial), and the University of Cambridge (UoC). Study 1, completed in July 2024, assessed the effectiveness of objective and subjective dietary intake assessment methods in highly-controlled clinical trial (protocol published at https://doi.org/10.12688/f1000research.155683.1) and informed the design of study 2.
Study 2 is led and sponsored by UoR. All study activities will be conducted remotely, with participants taking part from their usual locations (e.g., home, work).
►Screening and Welcome Week
Participants will use the online REDCap research platform to provide informed consent and complete a screening questionnaire to determine eligibility. Eligible participants will be contacted by a study researcher to discuss the study requirements, confirm consent, and schedule the study period.
A week before starting the 5-week study (Welcome Week), participants will be sent study materials/equipment and will be referred to the SODIAT webpage to view online video tutorials and read user guidelines for each study tool. Afterwards, participants will attend a video call with a study researcher to familiarize them with the study protocol and provide an opportunity to ask questions.
During the Welcome Week, participants will also self-collect a baseline blood sample (pre-video call) and complete the online eNutri FFQ to assess habitual diet. Within 2 days, they will then complete a condensed version of the FFQ to evaluate its effectiveness in estimating diet quality with reduced participant burden.
►5-week study period
Participants will follow their usual diet during weeks 1 \& 5 and record their diet using study tools (wearable cameras, blood samples, urine samples and online FFQ) for 3 consecutive days (Monitoring Weeks). During week 3 (Calibration Week), participants will use the same study tools as before whilst consuming the 3-day test diet. There will be two test diets (one diet for meat/fish consumers and another slightly adapted for non-consumers), consisting of foods and drinks that are common in the UK. During this controlled part of the study, participants will be requested to eat/drink all foods and drinks provided (delivered by an online supermarket) but cannot consume anything extra. They will receive recommendations on serving sizes for each food/drink but participants can choose how much they eat (either more or less).
►Wearable cameras
Participants will wear a small camera unit mounted on glasses (or attached to their own frames) during the 3-day periods of weeks 1, 3, and 5 (days 1-3; 15-17 and 32-34). The camera automatically captures still images every 7 seconds to document food and drink intake. The camera will be worn from waking to going to bed, although participants will be instructed to remove the camera during private times (e.g., bathroom), sensitive locations (e.g., changing rooms, GP surgeries) and if unsafe to wear (e.g., driving), and log these occasions, as well as the camera start time, on a paper-based log. At the end of the study, encrypted SD cards containing the images will be returned to the research team at Imperial for secure processing.
Images will be pre-processed using AI to exclude irrelevant images, and blur identifying details (e.g., faces, device screens). Only anonymised images will be analysed by researchers to estimate dietary intake.
►Capillary blood samples
When fasted, participants will self-collect blood samples using OneDraw kits on day 4 of each study week (day 4, 18 and 35), which collect a few drops of blood from the upper arm/thigh onto a filter paper cartridge. A baseline sample will also be collected during the Welcome Week. Instructions and video tutorials will be provided, and samples will be mailed to researchers at UoC for storage and biomarker analysis.
►Spot urine samples
Over 4 consecutive days of each study week (days 1-4, 15-18, 32-35), participants will collect first morning void and last evening void urine samples using straw and vacuum tube kits. Samples will be temporarily stored in a refrigerator before mailing them to AberU for processing where biomarkers of food and drink intake will be analysed.
►Online FFQ (eNutri)
Participants will complete the online eNutri FFQ on six occasions. Both the original (long-format) and condensed FFQ will be completed during Welcome Week to capture habitual intake during the previous 4 weeks. During the study, a 3-day, condensed FFQ adapted to capture foods/drinks not well-represented by biomarker analysis, will be completed at the end of each recording week (day 4, 18 and 35). During the test diet week, the original FFQ, adapted to capture 3-day intakes, will also be completed (day 18). The FFQ inputs, nutrient and food group intakes, and diet quality data will be exported in pseudonymised format for analysis.
At the study's conclusion, participants will complete a short, online usability questionnaire about the study tools via REDCap (day 35).
Participants will mail their blood and urine samples at designated timepoints using pre-paid postage, and return all study equipment and logs at the end of the study via a courier collection.
Researchers will monitor adherence and communicate with participants as needed. Daily reminders will also be sent via email or text (SMS) message during the recording days.
► Statistical analysis
Accuracy of integrating multiple dietary assessment technologies to report dietary intake in free living environments will be measured during the calibration week (week 3) using dietary intake data collected from wearable cameras, spot urine samples, capillary blood samples, and self-reported FFQs.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Free-living adults living in GB | – | Other: Measuring dietary intakeThe study aims to recruit 133 adults living in GB with BMI more than 18.5 kg/m2 who are fluent in English. Participants will monitor their usual dietary intake during two 3-day monitoring periods during weeks 1 and 5 by wearing camera technology, self-collecting blood and urine samples at designated times, and completing online food frequency questionnaire on multiple occasions. During the calibration week (week 3) participants will consume the same 3-day test diet (either the diet for meat/fish consumers or non-consumers, as identified at screening). |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- UK population.
Key inclusion criteria (3 listed)
- 18 years and older
- Lives in Great Britain (England, Schotland and Walse)
- Able to read/understand instructions written in English and are fluent in English
Key exclusion criteria (16 listed)
- Diagnosed or self-report as being underweight (have a body mass index (BMI) of less than 18.5 kg/m2)
- Are unwilling/unable to collect urine and blood samples, use the wearable camera as instructed and/or spend 20-30 min online recording what they've recently had to eat/drink on multiple occasions
- Are unwilling/unable to have a video call with a researcher with cameras turned on
- Are unwilling/unable to post samples on specific days and receive/send a larger parcel at the start/end of the study (note: all return packaging and postage will be provided by us and will include a courier delivery and collection)
- Are unwilling/unable to receive a single grocery delivery from Sainsbury's or Tesco online supermarkets (delivery to be arranged by us), includes living in a postcode area that cannot receive grocery deliveries from Tesco or Sainsburys as well as not having space to refrigerate and freeze items.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Measuring dietary intakeDuring 5-week study, participants will monitor their usual dietary intake during two 3-day periods (on weeks 1 and 5). During week 3 (calibration week) participants will consume a test diet. Wearable camera technology, self-collected blood and urine samples, and online FFQ (eNutri) will be used to monitor food intake during study weeks. Study tools as well as foods/drinks for the test diet will be delivered to each participant and they will be asked to comply with the study procedures in their home or working environment. Participants will post study samples and the study equipment/logs at designated times using pre-paid envelopes or a courier collection, respectively. | Other | Free-living adults living in GB |
Primary outcome
Dietary intake measured by wearable camera technology.
Time frame: Days 1- 3 (week 1), days 15-17 (week 3) and days 32-34 (week 5).
Wearable cameras will be worn by the participants during the study days. Images from wearable cameras will be analysed to estimate what foods and drinks were consumed during the study days, as well as estimating their portion sizes (grams per day).
Dietary intake measured by spot urine.
Time frame: Morning and evening spot urine samples collected over 4 consecutive days on weeks 1, 3 and 5 (days 1-4, 15-18, 32-35).
A range of biomarkers indicating what a person has eaten/drank will be measured in urine samples.
Dietary intake measured by blood sample.
Time frame: Samples collected at fasted state in the morning of days 4, 18 and 35 (weeks 1, 3 and 5).
A range of food/drink biomarkers will be measured in capillary blood samples to indicate what a person has eaten/ drank.
Monitoring/calibration week dietary intake (condensed 3-day FFQ).
Time frame: Days 4, 18 and 35 (weeks 1, 3 & 5).
Food/drink intake during the 3-day study periods will be measured by the 3-day condensed FFQ (adapted to capture foods not represented by biomarker analysis). Outcomes include dietary intakes (frequency, portion size and grams per day) for each FFQ item, nutrient intakes, food group intakes and diet quality score.
4 secondary outcomes
Habitual dietary intake (original eNutri FFQ).
Time frame: Baseline.
Habitual dietary intake (condensed original FFQ).
Time frame: Baseline, after original eNutri FFQ.
Calibration week dietary intake (3-day eNutri FFQ).
Time frame: Day 18, week 3.
Usability questionnaire for each research tool.
Time frame: Day 35, week 5.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Sep 2026.
- SODIAT webpageLink provided by the sponsor.
- Individual participant dataSharing planned: Yes. Anonymised individual participant data will be shared in accordance with confidentiality and consent agreements. This may include: sociodemographic information, anthropometric measurements, dietary intake data, blood and urine biomarkers. Public data repositories (to be agreed by the project team) will be used preserving fully anonymised individual data.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Manfred Beckmann, Dr principal investigator
Department of Life Sciences, Aberystwyth University
Julie A Lovegrove, Professor principal investigator
Hugh Sinclair Unit of Human Nutrition Department of Food and Nutritional Sciences, University of Reading
Gary Frost, Professor principal investigator
Nutrition Research Section, Hammersmith Hospital Campus, Imperial College
4 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Dietary Intake Assessment and Food Intake Measurement, run by University of Reading at 4 sites in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 16 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 16 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 4 sites in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Dietary intake measured by wearable camera technology. (time frame: Days 1- 3 (week 1), days 15-17 (week 3) and days 32-34 (week 5).). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Sep 2026.