- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05635825
Energy and Nutrient Profiles When Asians Transit From a Meat-based to a Plant-based Diet: A Modelling Exercise
November 23, 2022 updated by: JeyaKumar Henry, Clinical Nutrition Research Centre, Singapore
This study aims to model and present a simulation exercise to assess the nutritional effects of replacing meat-based protein with meat analogues.
The hypothesis of our study is to understand if any positive or detrimental effects on nutrition and health will ensue, when people replace a meat-based diet with plant-based and alternative protein substitutes.
Study Overview
Detailed Description
A total of up 100 participants (Chinese/Malay/Indian), non-vegetarians, aged between 21 to 99 years, literate and numerate will be recruited for this study.
Participants will be required to complete a 4-day food record as part of the exercise.
To ensure accuracy of food records, participants will be requested to either weigh their foods or take photographs of all food and drink consumed during the duration of the study.
After all the food records have been collected, the data will be analysed using food composition tables.
Nutritional profiles of all participants will be generated.
Animal-based products will then be substituted with plant-based counterparts and a new nutritional profile will be generated for each participant.
Study Type
Observational
Enrollment (Actual)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Singapore, Singapore, 117599
- Clinical Nutrition Research Centre
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
17 years to 95 years (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Healthy Asian, non-vegetarian, literate and numerate participants aged between 21-99 years.
Description
Inclusion Criteria:
- Healthy males and females
- 21-99 years old
- Non-vegetarians
- Access to smart phone devices if participants intend to use photographic methods
Exclusion Criteria:
- Non-english speaking
- Members of any vulnerable populations
- Members of the research team or their immediate family members. Immediate family member is defined as a spouse, parent, child, or sibling, whether biological or legally adopted
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy Asian
Healthy Asian, non-vegetarian that is aged between 21 to 99, literate and numerate.
|
Collection of a 4-day food record
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Protein
Time Frame: 4 days
|
Food record of dietary protein intake
|
4 days
|
|
Carbohydrates
Time Frame: 4 days
|
Food record of carbohydrate intake
|
4 days
|
|
Fats
Time Frame: 4 days
|
Food record of fat intake
|
4 days
|
|
Minerals
Time Frame: 4 days
|
Food record of mineral intake
|
4 days
|
|
Dietary fibre
Time Frame: 4 days
|
Food record of dietary fibre intake
|
4 days
|
|
Cholesterol
Time Frame: 4 days
|
Food record of cholesterol intake
|
4 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 5, 2021
Primary Completion (Actual)
November 20, 2021
Study Completion (Actual)
November 28, 2021
Study Registration Dates
First Submitted
November 23, 2022
First Submitted That Met QC Criteria
November 23, 2022
First Posted (Actual)
December 2, 2022
Study Record Updates
Last Update Posted (Actual)
December 2, 2022
Last Update Submitted That Met QC Criteria
November 23, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2021-110
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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