Empowering Consumers to 'PREVENT' Diet-related Diseases Through 'OMICS' Sciences
NCT04590989 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100
Last updated 2021-07-15
Summary
The over-all aim of this 10-week randomized-controlled study, taking place only in Denmark, is to examine whether the PREVENTOMICS platform integrated in an e-commerce digital tool created to deliver personalized meals and dietary advices is able to produce more favorable health effects than meals based on general dietary recommendations in overweight subjects with elevated waist circumference.
Conditions
- Overweight
- Obesity
- Metabolic Syndrome
Interventions
- OTHER
-
Personalized Nutrition Plan
* Personalized breakfasts and dinners designed and cooked by Simplefeast, delivered twice a week (eaten 6 days per week) + access to Simplefeast's App for recipes of other meals not provided (i.e. lunches and Saturdays) which are designed to match the individual nutritional recommendations. * Personalized behavioral change program via electronic push notifications by ONMI
- OTHER
-
Non-Personalized Nutrition Plan
* Standard meals of breakfasts and dinners designed and cooked by Simple feast, based on general dietary recommendations, and delivered to participants twice a week. In addition, they will also have access to Simple feast's recipe App for other meals not provided. The recipes presented are generic, not personalized. * Subjects in the control group will also be enrolled in the behavioral program by ONMI, but the program will not be personalized nor based on the same behavior change methodology as in the PP group. In other words, the control group will get information more than is triggered to take actual action (i.e. general guidelines that is available from the National Health Service and World Health Organization).
Sponsors & Collaborators
-
Fundació Eurecat
collaborator OTHER -
Simple Feast
collaborator UNKNOWN -
Alimentómica
collaborator UNKNOWN -
University of Parma
collaborator OTHER -
ONMI
collaborator UNKNOWN -
University of Copenhagen
lead OTHER
Principal Investigators
-
Mads F Hjorth, PhD · University of Copenhagen
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-10-26
- Primary Completion
- 2021-06-14
- Completion
- 2021-06-14
Countries
- Denmark
Study Locations
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