- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07371559
Assessment of Food Intake Using Both 3D Scanning Method and a Photographic Method
Assessment of Calories in the Diets Using 3D Scanning and a Photographic Method
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: John Roger Speakman, PhD
- Phone Number: 15810868669
- Email: j.speakman@abdn.ac.uk
Study Contact Backup
- Name: Ying Yu, PhD
- Phone Number: 18513508048
- Email: y.yu@siat.ac.cn
Study Locations
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Guangdong
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Shenzhen, Guangdong, China
- Recruiting
- Shenzhen Institute of Advanced Technology
-
Contact:
- John Speakman, PhD
- Phone Number: 13466654659
- Email: j.speakman@abdn.ac.uk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Recently measured body mass index (BMI): normal control group (21.5 ≤ BMI < 25); Recently measured body mass index (BMI): healthy underweight group (15 < BMI ≤ 18.5); Must be able to choose the food as requested.
Exclusion Criteria:
Metabolic diseases; Recent weight loss due to various disease causes; Ongoing treatment for weight loss; Eating disorders; Pregnant or lactating women; Infectious diseases such as HIV, Hepatitis; Diabetes mellitus.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Control
21.5≤BMI<25, age between 25-40 years old, 100subjects.
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Superlean
15<BMI≤18.5, age between 25-40 years old, 100 subjects.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
BMI of the volunteers
Time Frame: This study will take about 1 year and a half to finish, starting from May 1 2025 to Dec 31 2026.
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The volunteers' BMI is chosen between normal and underweight for easy comparison.
|
This study will take about 1 year and a half to finish, starting from May 1 2025 to Dec 31 2026.
|
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3D scanning of the foods chosen by volunteers using a Bodyscan3d smartphone application
Time Frame: This study will take about 1 year and a half to finish, starting from May 1 2025 to Dec 31 2026.
|
The volunteers will be asked to choose 5 out of 20 dishes in a buffet and 3D scanning of the foods chosen by volunteers will be taken using a Bodyscan3d application.
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This study will take about 1 year and a half to finish, starting from May 1 2025 to Dec 31 2026.
|
|
Weight and name of each food
Time Frame: This study will take about 1 year and a half to finish, starting from May 1 2025 to Dec 31 2026.
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The weight and name of the food selected by the volunteers will be systematically recorded using a digital electronic scale and food record form.
This scale and food record form will be employed to ensure accurate measurements of each food item's mass that the volunteers consume throughout the study period and each food item they choose.
|
This study will take about 1 year and a half to finish, starting from May 1 2025 to Dec 31 2026.
|
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Calories of the food chosen by the volunteers will be evaluated using the Hava smartphone application
Time Frame: This study will take about 1 year and a half to finish, starting from May 1 2025 to Dec 31 2026.
|
We use another Hava application to evaluate the calories of the food selected by the volunteers and compare with the calories we calculated, with the smaller the difference, the better the Hava assessment.
|
This study will take about 1 year and a half to finish, starting from May 1 2025 to Dec 31 2026.
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SIAT-IRB-250215-H0960
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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